EXHIBIT 10.35
CONFIDENTIAL TREATMENT REQUESTED. CONFIDENTIAL PORTIONS
OF THIS DOCUMENT MARKED [****] HAVE BEEN REDACTED AND HAVE BEEN
FILED SEPARATELY WITH THE U.S. SECURITIES AND EXCHANGE COMMISSION
LICENSE AND COLLABORATION AGREEMENT
BETWEEN
ATHEROGENICS, INC.
AND
IPR PHARMACEUTICALS, INC.
DECEMBER 22, 2005
THIS CONFIDENTIAL DOCUMENT IS SUBJECT TO A NONDISCLOSURE AGREEMENT
BETWEEN THE PARTIES HERETO AND MAY NOT BE VIEWED BY, COPIED FOR OR
DISTRIBUTED TO ANY PERSON NOT SUBJECT TO SUCH NONDISCLOSURE
AGREEMENT OR NOT AUTHORIZED BY THE PARTIES HERETO.
TABLE OF CONTENTS
Page
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1. DEFINITIONS.................................................................................... 1
2. PRODUCT DEVELOPMENT............................................................................ 17
2.1 Development Plan 17
2.2 Development Activities of the Parties 18
3. REGULATORY MATTERS............................................................................. 20
3.1 Regulatory Strategy 20
3.2 Regulatory Responsibility in General 20
3.3 Regulatory Authority Communications and Cooperation Between the Parties 23
3.4 Communications Concerning Product 24
3.5 Records 24
3.6 Safety Matters 25
4. COMMERCIALIZATION.............................................................................. 25
4.1 Global Commercialization Team and U.S. Commercialization Team 25
4.2 Commercially Diligent Efforts 25
4.3 Commercialization Plan 26
4.4 Commercialization Activities of the Parties 26
4.5 Commercial Manufacturing and Supply of Products 27
5. DILIGENCE AND COOPERATION...................................................................... 27
5.1 Information Sharing 27
5.2 Diligence Requirements 28
5.3 Failure To Use Diligence 29
6. GOVERNANCE..................................................................................... 29
6.1 General 29
6.2 Alliance Managers 29
6.3 Committees 30
7. LICENSES AND COVENANTS......................................................................... 34
7.1 License Grants to AstraZeneca 34
7.2 License Grants to AGIX 35
7.3 Rights Acquired from Third Parties 35
7.4 Covenants Concerning the Products, the Compound and the Field 36
8. PAYMENTS AND REPORTS........................................................................... 39
8.1 Upfront Payment 39
8.2 Milestone Payments 39
8.3 Royalties 41
8.4 Adjustments and Changes to Royalty Rates in Certain Circumstances 44
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8.5 Payment; Report 48
8.6 Exchange Rate; Manner and Place of Payment 48
8.7 Representations and Covenants Concerning Certain Matters 51
9. INTELLECTUAL PROPERTY.......................................................................... 51
9.1 Ownership of Inventions; Obligation to Update 51
9.2 IPC53 52
9.3 Patent Prosecution 55
9.4 Patent Marking 57
9.5 Infringement by Third Parties 57
9.6 Infringement of Third Party Rights 59
9.7 Cooperation 59
9.8 Awards and Recovery 60
9.9 Costs 60
9.10 Trademarks 61
10. CONFIDENTIALITY................................................................................ 62
10.1 Nondisclosure Obligation 62
10.2 Permitted Disclosures 63
10.3 Use of Name 64
10.4 Publicity 64
10.5 Publications 65
11. REPRESENTATIONS AND WARRANTIES................................................................. 65
11.1 Corporate Existence and Authority 65
11.2 Authorized Execution; Binding Obligation 65
11.3 No Conflicts 65
11.4 All Consents and Approvals Obtained 66
11.5 AGIX Representations and Warranties. AGIX represents and warrants to AstraZeneca as
follows: 66
11.6 Other Agreements 68
11.7 Debarment 68
11.8 Knowledge of Pending or Threatened Litigation 69
11.9 Pre-Existing Third Party Licenses 69
11.10 Disclaimer of Implied Warranties 70
11.11 Limitation of Liability 70
11.12 Guarantee of Performance of Affiliates 70
12. INDEMNIFICATION................................................................................ 71
12.1 AstraZeneca Indemnification 71
12.2 AGIX Indemnification 71
12.3 Indemnification Procedures 72
12.4 Indemnification Payment Adjustments 73
12.5 Indemnification Payment 74
12.6 Survival 74
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13. TERM AND TERMINATION........................................................................... 74
13.1 Term 74
13.2 Condition Precedent 74
13.3 Termination by AstraZeneca 75
13.4 Termination for Material Breach or Bankruptcy 76
13.5 Effects of Termination 77
13.6 Non-Exclusive Rights 81
13.7 Rights in Bankruptcy 81
13.8 Accrued Rights and Obligations; Survival 81
14. DISPUTE RESOLUTION............................................................................. 82
14.1 Procedure 82
14.2 Alternative Dispute Resolution 82
14.3 Arbitration Procedure 83
14.4 Special Rules for Disputes Concerning Diligence Covenant 84
15. MISCELLANEOUS.................................................................................. 84
15.1 Standstill 84
15.2 Termination of Certain Rights Upon AGIX Change of Corporate Control 84
15.3 Assignment 85
15.4 Force Majeure 86
15.5 Further Assurances 86
15.6 Severability 86
15.7 Notices 86
15.8 Jurisdiction and Venue 87
15.9 Affiliates 87
15.10 Entire Agreement 87
15.11 Headings 87
15.12 Independent Contractors 87
15.13 Waiver 88
15.14 No Third Party Beneficiaries 88
15.15 Cumulative Remedies 88
15.16 Counterparts 88
15.17 Waiver of Rule of Construction 88
Exhibit 1A ....... AGIX Compound Patents
Exhibit 1B ....... Co-Promotion Agreement
Exhibit 1C ....... Other AGIX Patents
Exhibit 1D ....... Pre-Existing Third Party Licenses
Exhibit 1E ....... Probucol Analog
Exhibit 1F ....... Transition Services Agreement
Exhibit 11.5 ..... Disclosure Concerning AGIX Representations and Warranties
iii
LICENSE AND COLLABORATION AGREEMENT
This LICENSE AND COLLABORATION AGREEMENT (the "AGREEMENT") is made and is
effective as of December 21, 2005 (the "EXECUTION DATE") by and between
ATHEROGENICS, INC., a corporation organized and existing under the laws of the
State of Georgia ("AGIX"), and IPR PHARMACEUTICALS, INC., a corporation
organized and existing under the laws of Puerto Rico ("ASTRAZENECA").
RECITALS
A. AGIX is engaged in manufacturing, research and development of
pharmaceutical products and is currently engaged in the development of AGI-1067.
B. AstraZeneca is engaged in the research, development, manufacture and
marketing of pharmaceutical products. AGIX and AstraZeneca wish to collaborate
in the further clinical development and marketing of the Compound, upon the
terms described in this Agreement and the Related Agreements (as defined
herein).
NOW, THEREFORE, in consideration of the foregoing premises and the mutual
covenants herein contained, the Parties hereby agree as follows:
1. DEFINITIONS
When used and capitalized in this Agreement (other than the headings of
the Sections and subsections), including the foregoing recitals, the following
terms shall have the meanings assigned to them in this Section and include the
plural as well as the singular. All financial and accounting terms not otherwise
defined in this Agreement, whether capitalized or not, shall have the meanings
assigned to them in accordance with generally accepted accounting principles
based on International Accounting Standards/International Financial Reporting
Standards as in effect from time to time ("GAAP").
"Accelerated Assumption Payment" has the meaning provided in Section
3.2(c)(i) hereof.
"Action" has the meaning provided in Section 12.3(a) hereof.
"ADR" has the meaning provided in Section 14.2 hereof.
"ADR Request" has the meaning provided in Section 14.2(a) hereof.
"Adverse Event" means any adverse medical occurrence in a patient or
clinical investigation subject administered a pharmaceutical product and that
does not necessarily have to have a causal relationship with any treatment,
including as designated under 21 C.F.R. Section 312.32 and any other Applicable
Laws.
"Adverse Event Report" means any oral, written or electronically
transmitted report of any Adverse Event.
"Affiliate" means any Person that directly (or indirectly through one or
more intermediaries) controls, is controlled by, or is under common control with
a Party. For purposes of this definition only, the terms "controls,"
"controlled," and "control" means (i) the direct or indirect ability or power to
direct or cause the direction of the management and policies of an entity or
otherwise direct the affairs of such entity, whether through ownership of
equity, voting securities, or beneficial interest, by contract, or otherwise, or
(ii) the ownership, directly or indirectly, of at least 50% of the voting
securities (or other comparable ownership interest for an entity other than a
corporation) of a Party.
"AGIX Compound Patents" mean those Patents listed in Exhibit 1A, including
all foreign counterparts thereof, as supplemented and updated from time to time
pursuant to Section 9.1(c) hereof.
"AGIX Indemnitees" has the meaning provided in Section 12.1 hereof.
"AGIX IP" means the Licensed Patents and AGIX Know-How.
"AGIX Know-How" means Know-How Controlled by AGIX or any of its Affiliates
on or after the Effective Date that is necessary or useful for the research,
Development, Manufacture, Commercialization, use, sale, offer for sale or
importation of the Compound and Products in the Field.
"AGIX Losses" has the meaning provided in Section 12.1 hereof.
"Alliance Manager" has the meaning provided in Section 6.2 hereof.
"Annualized Quarterly Net Sales" means the Net Sales for a given Calendar
Quarter multiplied by four (4).
"Applicable Laws" means all applicable statutes, ordinances, regulations,
rules, or orders of any kind whatsoever of any Governmental Authority,
including, without limitation, the FD&C Act, Prescription Drug Marketing Act,
Generic Drug Enforcement Act of 1992 (21 U.S.C. Section 335a et seq.), and
Anti-Kickback Statute (42 U.S.C. Section 1320a-7b et seq.), all as amended from
time to time in the Territory.
2
"Approvable Letter" means a written communication from the FDA to the
owner of the application for Regulatory Approval stating that the FDA will not
approve the application, or that the FDA will approve the application if
additional information is submitted or specific conditions are met, pursuant to
21 C.F.R. Section 314.3(b).
"Arbitration Panel" has the meaning provided in Section 14.3(a) hereof.
"ARISE Results" means the statistical summary tables for efficacy and
safety of the unblinded efficacy and safety results from the ARISE Study, which
summary tables are determined by a Third Party statistician, mutually agreed to
by the Parties in advance, to be complete and final, analyzed in accordance with
the last Statistical Analysis Plan submitted to the FDA before locking the
database of the ARISE Study for unblinding.
"ARISE Study" means the pivotal Phase III Study being conducted by AGIX
known as ARISE.
"AstraZeneca Indemnitees" has the meaning provided in Section 12.2 hereof.
"AstraZeneca IP" means AstraZeneca Patents and AstraZeneca Know-How.
"AstraZeneca Know-How" means Know-How Controlled by AstraZeneca or any of
its Affiliates that is necessary or useful for the research, Development,
Manufacture, Commercialization, use, sale, offer for sale or importation of the
Compound and Products in the Field.
"AstraZeneca Losses" has the meaning provided in Section 12.2 hereof.
"AstraZeneca Patents" means any Patents Controlled by AstraZeneca or any
of its Affiliates on or after the Effective Date that are necessary or useful
for the Development, Manufacture, Commercialization, use, sale, offer for sale
or importation of the Compound or any Product in the Field.
"Assumption Date" means the earlier of (i) the date of receipt of U.S. NDA
Approval for the First Product and (ii) the date AstraZeneca pays to AGIX the
Accelerated Assumption Payment.
"Blocking Patent" means a patent owned or controlled by a Third Party that
contains a Valid Patent Claim that (a) is necessary for the Manufacture or sale
of a Compound or Product; and (b) the Development, use, Manufacture, sale, offer
for sale or importation of such Compound or Product would infringe such Third
Party's patent rights but for the grant of a license to such rights by such
Third Party.
"Business Combination" means any merger, consolidation, sale or transfer
of all or substantially all of the assets, or other similar transaction to which
AGIX is a party unless, following such transaction or transactions, (i) the
individuals and entities who
3
were the beneficial owners of the outstanding voting securities of AGIX
immediately prior to such transaction beneficially own, directly or indirectly,
more than fifty percent (50%) of the combined voting power of the then
outstanding voting securities entitled to vote generally in the election of
directors or similar governing persons of the corporation or other entity
resulting from such transaction ("SUCCESSOR") in substantially the same
proportions as their ownership immediately prior to such transaction of such
outstanding voting securities, and (ii) at least fifty percent (50%) of the
members of the Board of Directors or similar governing body of the Successor
were members of the Board of Directors of AGIX at the time of the execution of
the initial agreement, or the action of the Board of Directors of AGIX,
providing for such transaction.
"Business Day" means any day other than a Saturday, Sunday or any day that
is a banking holiday in the United States, United Kingdom or Puerto Rico.
"Calendar Quarter" means the respective periods of three (3) consecutive
calendar months ending on March 31, June 30, September 30 and December 31.
"Calendar Year" means each successive period of twelve (12) months
commencing on January 1 and ending on December 31.
"cGCP" means the then current good clinical practices as defined in U.S.
Regulations 21 C.F.R. Sections 50, 54, 56, 312 and 314, (or in the case of
foreign jurisdictions, comparable regulatory standards), the International
Conference of Harmonization (ICH) E6 "Good Clinical Practice: Consolidated
Guidance," and in any successor regulation or any official guidance documents
issued by a Regulatory Authority.
"cGLP" means the then current good laboratory practice standards as
defined by the FDA pursuant to 21 C.F.R. Part 58 (or in the case of foreign
jurisdictions, comparable regulatory standards), and in any successor regulation
or any official guidance documents issued by a Regulatory Authority.
"cGMP" means the then-current good manufacturing practices as defined by
the FDA pursuant to 21 C.F.R. Sections 210 and 211 and/or the current
EC-GMP-Directives and relevant EC guidelines and the ECC-GMP-Guide and in any
successor regulation or any official guidance documents issued by a Regulatory
Authority.
"Change of Corporate Control" means the occurrence of either of the
following:
(a) a Business Combination involving AGIX; or
(b) a change in the beneficial ownership of fifty percent (50%) or
more of AGIX's voting securities (whether in a single transaction or
series of related transactions) where, immediately after giving effect to
such change, the legal or beneficial owner of more than fifty percent
(50%) of AGIX's voting securities is a Third Party or Group, excluding any
equity investments by venture capitalists or
4
investment banks or other non-strategic investors, who alone or with their
Affiliates, are not themselves in the business of developing and
commercializing pharmaceutical products.
"Coated Stent" means a stent coated with a Product for use in the Field.
"Combination Product" means a Product in final form that includes one or
more pharmaceutically active ingredients other than the Compound, in combination
with the Compound that are sold as a fixed dose or separate doses in a single
package and priced as one item. All references to Product in this Agreement
shall be deemed to include Combination Product(s).
"Commercialization" means all appropriate activities undertaken before and
after Regulatory Approval pursuant to an approved Commercialization Plan for a
Product or otherwise relating specifically to the marketing, sale and
distribution of Products including, without limitation, (i) sales force
detailing, advertising, education, planning, marketing, sales force training and
distribution, and (ii) scientific and medical affairs.
"Commercialization Plan" has the meaning provided in Section 4.3(a)
hereof.
"Commercially Diligent Efforts" means, with respect to the research,
Development, Manufacture or Commercialization by a Party of a Compound or
Product, as the case may be, efforts and resources reasonably used by an entity
of similar resources and expertise as such Party (and in the case of
AstraZeneca, AstraZeneca or its Affiliates), for such similar entity's own
compounds or products (including internally developed, acquired and in-licensed
compounds or products) with similar commercial potential at a similar stage in
their lifecycle (assuming continuing development of such product), taking into
consideration their safety, tolerability and efficacy, the competitiveness of
alternative products, the likelihood of Regulatory Approval, their profitability
(taking into account any payments payable under this Agreement), the extent of
market exclusivity, cost to develop the Compound or Product, health economic
claims, and other similar factors reasonably determined by AstraZeneca to be
relevant. If, at the time of measurement of Commercially Diligent Efforts, the
efforts and resources used by AGIX or AstraZeneca and their Affiliates, as the
case may be, for such entity's own similar compounds and products (other than
the Compound and the Product(s)) are greater than those used by an entity of
similar resources and expertise, then "Commercially Diligent Efforts" shall mean
such entity's level of effort and resources, rather than the efforts and
resources used by an entity with similar resources and expertise.
"Compete" means, with respect to a pharmaceutical product, that such
product is in the same Uniform System of Classification (USC) class as another
product, as reported by IMS or any comparable successor agency.
5
"Competing Generic Product" means, with respect to a Product, a product
(i) having the same active pharmaceutical ingredient as the Compound, and (ii)
that has been approved by applicable Regulatory Authorities for sale in the
Field; provided, however, that a Competing Generic Product shall not include any
product being sold or offered for sale by AstraZeneca or any AstraZeneca
Affiliate.
"Competing 1067 Product" means any pharmaceutical product that Competes
with the Product.
"Compound" means AGI-1067, which is [****]; including its
pharmacologically acceptable salts, solvates, hydrates, hemihydrates,
polymorphs, metabolites, free base forms, pro-drugs, esters, tautomers and if
applicable, any isomers, stereoisomers, racemates, enantiomers and all optically
active forms thereof.
"Compound-Only Issue" means an issue relating to an AGIX Compound Patent
or a claim included within an AGIX Compound Patent that in either case claims,
or is directed to, solely the Compound or solely a Product.
"Compulsory Sublicense" means a sublicense of the rights granted in this
Agreement entered into by AstraZeneca or an AstraZeneca Affiliate because a
court or other governmental agency of competent jurisdiction has required
AstraZeneca or an AstraZeneca Affiliate to grant to a Third Party rights to
make, have made, use sell, offer to sell or import the Product in a country in
the Territory; provided, however, that any such requirement shall not include a
requirement by a court or other governmental agency of competent jurisdiction
resulting from a merger with or acquisition of or by another company or entity
involving AstraZeneca, or the acquisition by AstraZeneca of other products.
"Confidential Information" has the meaning provided in Section 10.1
hereof.
"Control" or "Controlled" means, with respect to any intellectual property
right, that the Party or its Affiliate owns or has a license to such
intellectual property right and has the ability to grant access, a license, or a
sublicense to such intellectual property right to the other Party as provided
for in this Agreement without violating an agreement with, or infringing any
rights of, a Third Person.
"Co-Promotion Agreement" means the Co-Promotion Agreement between
AstraZeneca Pharmaceuticals LP and AGIX dated as of the Execution Date and
attached hereto as Exhibit 1B.
"De Minimis Amount" has the meaning provided in Section 15.1 hereof.
"Development" means the conduct of all activities that are reasonably
required to obtain Regulatory Approval or create other Indications for a
Product, including, without limitation: (i) toxicology, in vitro testing, in
vivo testing, in silico testing, stability testing,
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[****] indicates that certain confidential information contained in this
document has been omitted pursuant to a request for confidential treatment and
filed separately with the Securities and Exchange Commission.
6
statistical analysis and report writing, packaging and regulatory affairs,
pre-clinical studies and clinical trials in accordance with, to the extent
applicable, the cGLPs, cGCPs and cGMPs or other designated quality standards and
Applicable Laws; (ii) all activities relating to developing the ability to
Manufacture the Compound and Product, including, without limitation,
formulation, delivery technologies and devices, bulk production, fill/finish,
Manufacturing process development, and Manufacturing and quality assurance
technical support; (iii) Manufacture of clinical supplies of the Compound; and
(iv) all interactions with any Regulatory Authority regarding the foregoing.
"Development Budget" means the budget for Development activities that is
included within each Development Plan, as such budget may be amended or updated
from time to time in accordance with Section 2.1(d).
"Development Costs" means the reasonable costs incurred by a Party or its
Affiliates for Development of Product(s), as in accordance with the Development
Plan, including without limitation (to the extent included in the Development
Plan): (a) all out-of-pocket costs and expenses, including without limitation
payments to investigators and contract research organizations, data management,
statistical design and analysis, and document preparation; (b) fees incurred in
connection with filings related to Regulatory Approvals; (c) the costs and
expenses of clinical supplies for such efforts as set forth in the Development
Plan, including the cost of clinical supplies of Products, costs and expenses
incurred to purchase or package combination drugs or devices, and costs and
expenses of disposal of clinical samples; (d) the costs of internal scientific,
medical, technical or managerial personnel necessary to conduct the activities
set forth in the Development Plan; and (e) any other costs necessary to conduct
the activities described in the Development Plan.
"Development Plan Outline" means the outline of the minimum items to be
included in the Development Plan, which outline is contained in a letter
delivered by AGIX to AstraZeneca on the date hereof.
"Development Plan" means a written rolling three-year plan for the
Development of Product(s), including, without limitation, a budget for such
activities, as such plan may be amended or updated from time to time in
accordance with Section 2.1(d). The Initial Development Plan has been agreed
upon by the Parties and is included in a letter delivered by AGIX to AstraZeneca
on the date hereof.
"Development Program" means the activities undertaken by AGIX and
AstraZeneca as set forth in the Development Plan.
"Diabetes" means diabetes mellitus, insulin resistance, and complications
of diabetes, excluding the treatment of diabetic retinopathy using nonsystemic
preparations (such as eyedrops, intraocular injections or local ointments or
creams or eye patches).
"Dispute" has the meaning provided in Section 14.1(a) hereof.
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[****] indicates that certain confidential information contained in this
document has been omitted pursuant to a request for confidential treatment and
filed separately with the Securities and Exchange Commission.
7
"Drug Device" means a combination of the Product and a therapeutic device
and/or a device used to deliver the Compound.
"Effective Date" has the meaning provided in Section 13.2(a) hereof.
"Exchange Act" has the meaning provided in Section 15.1 hereof.
"Exclusive Market Product" means a product (other than a Product) sold or
offered for sale by a person other than AGIX in a country that is the subject of
a Valid Patent Claim directed to the composition of matter or use of such
product in such country.
"Expanded Field Indication" has the meaning provided in Section 7.4(a)
hereof.
"FDA" means the U.S. Food and Drug Administration, or any successor
federal agency having responsibility over U.S. Regulatory Approvals.
"FD&C Act" means the U.S. Federal Food, Drug, and Cosmetic Act, as amended
from time to time (21 U.S.C. Section 301 et seq.), together with any rules and
regulations promulgated thereunder.
"Field" means intravenous , injectable, solid and all other dosage or
delivery and therapeutic forms (oral and otherwise, and Drug Devices, such as
Coated Stents) to treat, prevent or control atherosclerosis and related
cardiovascular, renovascular, and cerebrovascular indications, including but not
limited to peripheral vascular disease, post- coronary artery by-pass graft
patency, restenosis following percutaneous coronary intervention, carotid artery
disease, acute coronary syndrome, heart failure, stroke, impaired renal
functions and Diabetes. "Field" shall not include any other indications not
described in the preceding sentence, including, without limitation, other
inflammatory and autoimmune diseases such as rheumatoid arthritis, asthma,
chronic obstructive pulmonary disease, psoriasis, inflammatory bowel disease,
and transplant vasculopathy, central nervous system diseases and other
ophthalmic diseases and conditions not expressly included in the Field, such as
treatment of diabetic retinopathy using nonsystemic preparations (such as
eyedrops, intraocular injections or local ointments or creams or eye patches).
"Final ARISE Results" has the meaning provided in Section 13.3(a).
"First Commercial Sale" means the date on which a Product is first shipped
in commercial quantities by AstraZeneca, its Affiliates, or Sublicensees, as the
case may be, for commercial sale to Third Persons (other than AstraZeneca's
Sublicensees) in a country in the Territory following Regulatory Approval of
such Product in such country.
"First Product" means the Product contemplated by the Initial Development
Plan.
8
"GAAP" has the meaning provided in the first paragraph of this Section 1.
"Generic Competition" means, for a Product sold in a country, a situation
where the following three conditions exist and continue:
(i) a court or agency of competent jurisdiction has cancelled or
held invalid or unenforceable claims under the Licensed Patents,
AstraZeneca Patents or Joint Patents prior to the expiration of the
Royalty Term for such country, such that a Third Party may, without
infringing any Licensed Patents, AstraZeneca Patents or Joint Patents and
without a license from or other agreement from AstraZeneca, sell a
Competing Generic Product in such country; provided, however, that Generic
Competition shall be considered to no longer be in effect if such decision
is reversed or modified such that any such claim in such Licensed Patent,
AstraZeneca Patent or Joint Patent is reinstated or revalidated on appeal;
(ii) a Competing Generic Product is being sold to the public in such
country pursuant to required approvals from applicable Regulatory
Authorities; and
(iii) the Net Sales of the Product in such country are reduced by at
least [****] compared with such Net Sales in such country immediately
preceding the sale of such Competing Generic Product in such country.
The comparison in clause (iii) above shall be measured for a given Calendar
Quarter by comparing Net Sales in such country for (A) the twelve-month period
immediately preceding and including the three months in such Calendar Quarter,
with (B) the twelve month period preceding and including the month immediately
preceding the month containing the date that AstraZeneca reasonably determines
as the date the Competing Generic Product was first offered for sale to the
public in such country, or was first shipped in such country in commercial
quantities following receipt for such Competing Generic Product of required
regulatory approvals from applicable Regulatory Authorities. Where less than
twelve (12) months of Net Sales for the Product has occurred prior to the first
sale of the Competing Generic Product, Net Sales shall be determined on an
annualized basis.
"Global Commercialization Team" means AstraZeneca's and its Affiliates'
team responsible for the commercialization of Products throughout the world.
"Governmental Authority" means any court tribunal, arbitrator, agency,
commission, official or other instrumentality of any federal, state, or other
political subdivision, or supranational body, domestic or foreign.
"Group" means a group of related Persons deemed a "person" for purposes of
Section 13(d) of the Securities Exchange Act of 1934, as amended.
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[****] indicates that certain confidential information contained in this
document has been omitted pursuant to a request for confidential treatment and
filed separately with the Securities and Exchange Commission.
9
"HSR" means the Xxxx-Xxxxx-Xxxxxx Antitrust Improvements Act of 1976, as
amended.
"Indemnifying Party" means the Party to whom the Indemnitee is entitled to
look for indemnification, pursuant to Section 12.3(a) hereto.
"Indication" means any use of the Product in the Field as approved by
Regulatory Authorities.
"Indication Fee" has the meaning provided in Section 7.4(a) hereof.
"Indication Information" has the meaning provided in Section 7.4(a)
hereof.
"Indirect Taxes" means value added taxes, sales taxes, consumption taxes
and other similar taxes.
"Initial Development Plan" means that development plan which AGIX has
previously agreed with the FDA will be completed prior to submission by AGIX of
an NDA for the Product, and which is contained in a letter delivered by AGIX to
AstraZeneca on the date hereof.
"IPC Patent Counsel" has the meaning provided in Section 9.2(b)(iv)
hereof.
"IPC" has the meaning provided in Section 6.3(h) hereof.
"JDC" has the meaning provided in Section 6.3(b) hereof.
"JMC" has the meaning provided in Section 6.3(a) hereof.
"Joint Inventions" has the meaning provided in Section 9.1(d) hereof.
"Joint Patents" has the meaning provided in Section 9.1(e) hereof.
"Know-How" means all tangible and intangible: (a) techniques, technology,
practices, trade secrets, discoveries, inventions, methods, formulas, knowledge,
know-how, skill, experience, tests, assays, test data and results (including
pharmacological, toxicological, pre-clinical and clinical test data and
results), technical, non-technical, analytical and quality control data, results
or descriptions, drawings, plans, diagrams, software and algorithms; and (b)
compounds, compositions of matter, cells, cell lines, assays, animal models and
physical, biological or chemical material that, in either case, is Controlled by
a Party or the Parties, or Affiliates of a Party on or after the Effective Date
and that is necessary or useful for the Development, Manufacture or
Commercialization of a Compound or Product.
"Knowledge of AGIX" means the actual knowledge of the following AGIX
employees: any Vice-President or Senior Vice-President of AGIX or higher, the
Chief
10
Executive Officer of AGIX and, with respect to intellectual property matters,
the Director of Legal Affairs and Intellectual Property, and, in the case of
each such officer, such additional knowledge as could be obtained upon
reasonable inquiry of AGIX employees and AGIX records.
"Licensed Patents" means AGIX Compound Patents and Other AGIX Patents.
"Licensed Probucol Analog" has the meaning provided in Section 7.4(b)
hereof.
"Major Market" means any of the following jurisdictions: [****].
"Manufacture" and "Manufacturing" means, with respect to a Product or
Compound, the synthesis, manufacturing, processing, formulating, packaging,
labeling, holding and quality control testing of such Product or Compound.
"Material Restructuring" means the transfer to any Third Party by either
Party of more than fifty percent (50%) of its fixed (tangible and intangible)
assets as shown on the balance sheet of the Party at December 31, 2005.
"Mixed Issue" means an issue relating to a Licensed Patent that is not a
Compound-Only Issue.
"NDA" means the single application or set of applications (and any other
required registrations, notifications, forms or supplements) for a Product
and/or pre-market approval to make and sell commercially a Product, filed with
the FDA or with a Regulatory Authority anywhere in the Territory.
"NDA Acceptance" means the acceptance in writing for regulatory filing of
a NDA by the FDA.
"Net Sales" means the gross invoiced amount on sales of Products to Third
Parties by AstraZeneca, its Affiliates, distributors and Sublicensees (except
for sales by Sublicensees who are parties to Compulsory Sublicenses and for
sales by AstraZeneca to Sublicensees), after deduction of the following items:
(a) discounts or rebates given that are consistent with
AstraZeneca's group accounting (except for bundled Products as provided below);
(b) amounts repaid or credited because of rejections, returns,
refunds, recalls and the like;
(c) rebates and similar payments made with respect to sales paid for
by any government or Regulatory Authority (except for bundled Products);
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[****] indicates that certain confidential information contained in this
document has been omitted pursuant to a request for confidential treatment and
filed separately with the Securities and Exchange Commission.
11
(d) [****] net of the amounts described in clauses (a), (b), (c)
and (e) in this definition, for transportation costs, distribution expenses,
special packaging and related insurance charges;
(e) taxes, excise taxes, Indirect Taxes, customs duties, customs
levies and import fees paid on the sale, importation, use or distribution of a
Licensed Product; and
(f) bad debts actually incurred.
Net Sales shall be calculated (i) using AstraZeneca's internal audited
systems used to report gross invoiced sales as adjusted for any of the items in
clauses (a) through (f) of the preceding sentence, and (ii) consistent with
GAAP, with the exception of bundled Products in clauses (a) and (c), and bad
debts in clause (f), of the preceding sentence. Where any discount or rebate
(including rebates or payments described in clause (a) or (c) of the first
sentence of this definition) is based on sales of a bundled set of products in
which a Product is included, the discount or rebate would be allocated as
actually credited unless the Product receives a higher than pro rata share of
the discount or rebate then the bundled product receives. In such case, the
Product discount or rebate shall be allocated to such Product on no greater than
a pro rata basis based on the sales value (i.e., the unit average selling price
multiplied by the unit volume) of the Product relative to the sales value
contributed by the other products in the bundled set with respect to such sale.
The calculation of Net Sales for Combination Products is set forth in
Section 8.4(f) hereof and shall be the sole method for calculating Net Sales for
such Combination Products.
"Noncompulsory Sublicense" means any sublicense of the rights granted in
this Agreement entered into by AstraZeneca or an AstraZeneca Affiliate, other
than a Compulsory Sublicense.
"Non-Exclusive Market Product" means a product sold or offered for sale by
a person other than AGIX in a country that is not the subject of any Valid
Patent Claim directed to the composition of matter or use of such product in
such country.
"Other AGIX Patents" means any Patents, other than AGIX Compound Patents,
Controlled by AGIX or any of its Affiliates on or after the Effective Date that
are necessary or useful for the Development, Manufacture, Commercialization,
use, sale, offer for sale or importation of the Compound or any Products in the
Field, including those Patents listed in Exhibit 1C and all foreign counterparts
thereof, as supplemented and updated from time to time pursuant to Section
9.1(d) hereof.
"Party" or "Parties" means AGIX and/or AstraZeneca.
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[****] indicates that certain confidential information contained in this
document has been omitted pursuant to a request for confidential treatment and
filed separately with the Securities and Exchange Commission.
12
"Patent" or "Patents" means (a) United States and non-United States patent
applications (including provisional applications, continuation applications,
continued prosecution applications, continuation-in-part applications,
divisional applications, substitute applications, or abandoned applications and
applications for certificates of invention), including without limitation patent
applications under the International Treaties and Conventions, including the
Patent Cooperation Treaty and the European Patent Convention; (b) any patents
issued or issuing from such patent applications (including certificates of
invention); (c) all patents and patent applications based on, corresponding to,
or claiming the priority date(s) of any of the foregoing; (d) any reissues,
substitutions, confirmations, registrations, renewals, patents of addition,
validations, re-examinations, additions, continuations, continued prosecution
applications, continuations-in-part, or divisionals of or claiming priority to
any of the foregoing; and (e) term extensions, supplementary protection
certificates and other governmental action which provide exclusive rights to a
product beyond the original patent expiration date.
"Person" means a natural person, a corporation, a partnership, a trust, a
joint venture, a limited liability company, any Governmental Authority or any
other entity or organization.
"Plaque Regression Claim" means the date that AstraZeneca or its
Affiliates (a) may through its sales representatives promote atherosclerotic
plaque regression in connection with the promotion of a Product in the United
States consistent and in accordance with the FD&C Act and (b) actually
authorizes its sales force to engage in such promotion.
"Pre-Existing Third Party Licenses" means the Patent Purchase Agreement
between Xxxxxxx Xxxxxxxxxxxxx, Ph.D. and AtheroGenics, Inc., dated April 26,
1995 and the License Agreement between Emory University and AtheroGenics, Inc.,
dated January 23, 1995, as amended August 3, 2005, as attached hereto as Exhibit
1D.
"Probucol Analog" has the meaning set forth in Exhibit 1E.
"Probucol Analog Fee" has the meaning provided in Section 7.4(b) hereof.
"Probucol Analog Information" has the meaning provided in Section 7.4(b)
hereof.
"Product" means a pharmaceutical product that contains or incorporates the
Compound, whether in development or approved by any Regulatory Authority,
including all formulations, line extensions and modes of administration
(including, without limitation, all delivery devices, dosage forms or other
peripherals and consumables), including, without limitation, Combination
Products.
13
"Product Complaint" means any written, verbal, or electronic expression of
dissatisfaction regarding a Product including, but not limited to, actual or
suspected product tampering, contamination, mislabeling, or wrong ingredients.
"Product Launch" shall mean the date on which the First Product is first
shipped in commercial quantities by AstraZeneca, its Affiliate or Sublicensee
for commercial sale to Third Persons in the Territory (not Affiliates or
Sublicensees) following Regulatory Approval of such Product.
"Product Trademarks" means (i) the Trademarks for or relating to any
Products and the registrations thereof, (ii) any pending or future Trademark
registration applications relating to the Products, (iii) any unregistered
Trademark rights relating to the Products as may exist through use prior to or
as of the date hereof, (iv) any current or future modifications or variants of
any of the foregoing rights, and (v) any future Trademarks adopted by
AstraZeneca or its Affiliates for use in connection with the Products.
"Promotable Diabetes Claim" means that AstraZeneca or its Affiliates (a)
may through its sales representatives promote treatment or prevention of
Diabetes in the United States consistent and in accordance with the FD&C Act and
(b) actually authorizes its sales force to engage in such promotion.
"Promotion" means those activities normally undertaken by a pharmaceutical
company's sales force to implement marketing plans and strategies aimed at
encouraging the appropriate use of a particular prescription or other
pharmaceutical product, including detailing. When used as a verb, "Promote"
means to engage in such activities.
"Promotional Materials" means any printed or other materials bearing a
Product name (trade name or generic name) used to promote Product, (examples
include, but are not limited to, all promotional brochures, journal ads,
brochures, selling aids, posters, reprints, video or audio tapes, press
releases, service items, managed care pull through sheets, formulary
presentations, price lists, monographs, Internet pages and websites, and
telephone, radio or television advertisements) and materials produced by outside
sources (examples include, but are not limited to, medical reprints, textbooks
and CME materials) to the extent funded by, created in cooperation with,
reviewed by or distributed by a Party, and any other items defined as labeling
or advertising in Section 201(m) of the FD&C Act or 21 C.F.R. Section
202.1(l)(1) (as such sections may be amended from time to time). "Promotional
Materials" shall also be deemed to include any advertising and promotional
labeling bearing the Parties' names but not bearing a Product name (examples
include "coming soon" or "reminder" advertisements) that may be used prior to
obtaining Regulatory Approval to market, sell and distribute a Product to
promote only the Indications of the Product.
"Prosecution" has the meaning provided in Section 9.3(a) hereof.
14
"Recent Monthly Net Sales" means an amount equal to the aggregate monthly
Net Sales of the Products during the last twelve (12) months preceding the date
that notice of termination is provided by AstraZeneca to AGIX, divided by twelve
(12).
"Regulatory Approval" means any and all approvals (including, to the
extent necessary, pricing approvals), licenses, registrations or authorizations
of any Regulatory Authority, necessary for the Development, Manufacture or
Commercialization of a Product.
"Regulatory Authority" means, in a particular country or jurisdiction, any
applicable government regulatory authorities involved in granting Regulatory
Approval of Product in such country or jurisdiction, including without
limitation, (a) in the United States, the FDA, and any other applicable
governmental or regulatory authority in the United States having jurisdiction
over Product, and any successor government authority having substantially the
same function, and (b) any non-United States equivalent thereof.
"Regulatory Materials" means any regulatory submissions, notifications,
registrations, approvals and/or other filings and correspondence made to or with
a Regulatory Authority, and any other records required to be maintained for
possible audit by a Regulatory Authority, that may be necessary or reasonably
desirable to Develop, Manufacture, market, sell or otherwise Commercialize
Products in the Territory.
"Related Agreements" means the Co-Promotion Agreement and Transition
Services Agreement entered into by the Parties contemporaneously with this
Agreement.
"Representatives" shall be deemed to include each Person that is or
becomes (i) an Affiliate of AstraZeneca, or (ii) an officer, director, employee,
attorney, advisor, accountant, agent or representative of AstraZeneca or of any
of AstraZeneca's subsidiaries or other Affiliates, providing such person is
acting on behalf of AstraZeneca.
"Royalty" or "Royalties" means the running royalties paid pursuant to
Section 8.3.
"Royalty Term" means, with respect to each Product, for each country in
the Territory, the period of time commencing on the First Commercial Sale of
such Product in any country and ending upon the expiration of the later of: (a)
the last Valid Patent Claim of a Licensed Patent, a Joint Patent or an
AstraZeneca Patent that would preclude a Third Party from developing, making,
using, selling or importing such Product in such country; and (b) ten (10) years
from the First Commercial Sale of such Product.
"Secondary Market" means the following countries: [****].
"Standard Sales Price" means the published sales price for the Product in
the relevant country.
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[****] indicates that certain confidential information contained in this
document has been omitted pursuant to a request for confidential treatment and
filed separately with the Securities and Exchange Commission.
15
"Sublicensee" means any Third Person (including, without limitation, a
distributor) to which a Party or any of its Affiliates grants any right to make,
use, market, or import and sell a Product in accordance with Section 7.1(c).
Notwithstanding the foregoing, a Third Person who is granted only the right to
distribute or promote a Product (such as a contract sales organization) shall
not be considered a Sublicensee.
"Successor" has the meaning provided in the definition of Business
Combination.
"Term" has the meaning provided in Section 13.1 hereof.
"Territory" shall mean all countries of the world.
"Third Party" or "Third Person" means any Person other than AGIX or
AstraZeneca and their respective Affiliates.
"Third Party Royalties" means upfront, milestone, royalty and any other
similar payments paid by AstraZeneca or any AstraZeneca Affiliate to any Third
Party for any Blocking Patent for the Development or Commercialization of
Compounds or Products, other than pursuant to a Pre-Existing Third Party
License.
"Trademark" means any trademark, trade dress, brand xxxx, trade name,
brand name, corporate name, logo or business symbol.
"Transition Services Agreement" means the Transition Services Agreement
between the Parties, dated as of the Execution Date and attached hereto as
Exhibit 1F.
"U.S." means the United States of America, including its territories and
possessions.
"U.S. Commercialization Team" means AstraZeneca's and its Affiliates' team
responsible for the commercialization of Products in the United States.
"U.S. NDA Approval" means approval by the FDA of the NDA filed with the
FDA relating to a Product.
"Valid Patent Claim" means a claim of an issued and unexpired Patent,
together with any patent term extension, supplementary protection certificate,
and/or regulatory approved period of exclusivity which has not been revoked or
held unenforceable or invalid by a decision of a court or other governmental
agency of competent jurisdiction, and which is not appealable or has not been
appealed within the time allowed for appeal, and which has not been disclaimed,
denied or admitted to be invalid or unenforceable through reissue,
re-examination, opposition, disclaimer or otherwise.
16
2. PRODUCT DEVELOPMENT
2.1 Development Plan
(a) Contents of the Development Plan. The Development Plan shall, to
the extent applicable, (i) identify the Product(s) to be Developed by the
Parties, including any Combination Product(s), Coated Stent(s) and other Drug
Devices; (ii) describe the overall program of Development for each such Product
through Regulatory Approval (A) in all Major Markets; (B) in the Secondary
Market taken as a whole; and (C) in other countries; (iii) describe the
Development activities of the Parties, including preclinical studies,
pharmacology, toxicology, ADME, formulation, Manufacturing of clinical supply,
clinical pharmacology studies, clinical studies and regulatory plans and other
key elements necessary to obtain Regulatory Approval for each such Product; (iv)
specify plans and protocols for clinical studies (including protocol outlines
for Phase IIIb and Phase IV clinical studies for label indication); and (v)
establish a schedule for all such activities. In addition, the Development Plan
shall include a detailed Development Budget that shall specify the Development
Costs for all Development activities covered by the Development Plan supported
by a financial business case.
(b) Initial Development. The Initial Development Plan is contained
in a letter delivered by AGIX to AstraZeneca on the date hereof.
(c) Additional Development . The Parties shall, within one hundred
eighty (180) days of the Effective Date, prepare a Development Plan, which shall
describe the Development activities in addition to those activities described in
the Initial Development Plan which will include additional Development
activities both before and after submission of the NDA for the First Product,
and an anticipated schedule for such activities. Such additional Development
Plan shall comply with Section 2.1(a) and shall be consistent with the
Development Plan Outline. The amendment shall become effective upon approval by
the JMC.
(d) Further Amendments to the Development Plan
(i) The JDC shall prepare for approval by the JMC amendments
and updates to the Development Plan at least once each Calendar Year.
(ii) Prior to the Assumption Date, notwithstanding anything
else in this Agreement to the contrary, no Development Plan or amendment to a
Development Plan shall be inconsistent with or contradict the Initial
Development Plan or Development Plan Outline; provided, however, that
AstraZeneca shall remain subject to the obligations set forth in Section
2.2(c)(i). In addition, no Development Plan shall obligate a Party to undertake
Development activities or expenditures beyond those
17
contemplated by the Initial Development Plan or Development Plan Outline without
the written agreement of such Party.
2.2 Development Activities of the Parties
(a) Compliance with the Development Plan. The Parties agree to use
Commercially Diligent Efforts to carry out Development of Product(s) in
accordance with the Development Plan under the direction and oversight of the
JDC; provided, however, that:
(i) Neither Party shall be obligated to incur Development
Costs in excess of the amounts allocated to such Party as specified in the
Development Plan;
(ii) The JMC shall be responsible for strategic planning
regarding Development of Products, and shall have the authority to approve the
Development of Coated Stent(s), identify Combination Products for which
Regulatory Approval will be sought, and identify any other potential Indications
or Products. The JMC shall be responsible for approval of amendments to and
updates of the Development Plan to provide for any such additional Products and
to oversee Development of any such Products; and
(iii) In no event shall the JDC or the JMC be authorized to
take any action, including approving any amendment to the Development Plan, that
would cause either Party to increase its Development Costs in excess of those
expressly contemplated by the Agreement or the then approved Development Plan
without the approval of such Party.
(b) AGIX Development Activities
(i) AGIX shall have responsibility, at its sole cost and at
the direction of the JDC, for Development, including without limitation
conducting and managing clinical studies, for those Development activities
described in the Initial Development Plan.
(ii) AGIX shall sponsor, prepare and submit, at its sole cost
and at the direction of the JDC, the U.S. NDA with respect to such First
Product; provided, however, that AstraZeneca shall cooperate and assist AGIX
with such filing.
(iii) AGIX may, at any time prior to the Assumption Date, in
its discretion and at its own expense, elect to sponsor and conduct a FOCUS
Study (Further Follow up Of AGI-1067 in ARISE Continuation as an Unblinded
Study) and/or a LOCATE Study (Limited Outcome Collection following ARISE for
Terminal Endpoints), unless the Parties otherwise agree to include either or
both such studies in the Development Plan, in which case AstraZeneca shall pay
the cost of such study or studies.
18
If AGIX elects to sponsor and conduct either such study or both studies, and if
AstraZeneca does not terminate the Agreement pursuant to Section 13.3(a), then
AstraZeneca shall thereafter be responsible for [****] of such Studies
(including costs incurred by AGIX prior to and subsequent to the date when
AstraZeneca elects not to terminate the Agreement pursuant to Section 13.3(a)).
(iv) AGIX shall have the right to Manufacture clinical
supplies of the Compound for its own Development activities pursuant to the
Development Plan.
(c) AstraZeneca Development Activities
(i) Except as set forth in Section 3.2(c), AstraZeneca shall
have responsibility, at its sole cost and at the direction of the JDC, for all
Development activities described in the Development Plan associated with the
Products that are not described in the Initial Development Plan, which shall
include conducting and managing a Carotid Intima Medial Thickness (CIMT) Study
(unless AstraZeneca can demonstrate that it would be commercially unreasonable
to do so).
(ii) Except as set forth in Section 3.2(c), AstraZeneca shall
have responsibility, at its sole cost and at the direction of the JDC, for all
Development activities described in the Development Plan necessary to seek
Regulatory Approval for the Products in the Territory outside the United States,
including without limitation conducting and managing clinical studies required
for Regulatory Approval in such countries.
(iii) The JDC shall identify, and the JMC shall have the
authority to approve as a part of the Development Plan, potential post-marketing
clinical studies, and AstraZeneca shall be responsible for conducting and
managing such post-marketing Clinical Studies, with AGIX assisting in such
management to the extent mutually agreed by the Parties.
(d) Cooperation
(i) Each Party shall assist the other Party in all Development
activities to the extent reasonably requested and mutually agreed to by the
Parties.
(ii) AstraZeneca shall be entitled, but not required, to have
three (3) representatives designated by AstraZeneca participate on AGIX's
Development team prior to U.S. NDA Approval. AGIX shall provide space at its
facility for such representatives to facilitate such participation.
(iii) AGIX shall be entitled, but not required, to have three
(3) representatives designated by AGIX participate on AstraZeneca's Development
team after U.S. NDA Approval. AstraZeneca shall provide space at its facility
for such representatives to facilitate such participation.
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[****] indicates that certain confidential information contained in this
document has been omitted pursuant to a request for confidential treatment and
filed separately with the Securities and Exchange Commission.
19
(e) Costs. Unless otherwise indicated in this Agreement or as
otherwise agreed to by the Parties, each Party shall bear its own costs in
connection with its activities under this Section.
3. REGULATORY MATTERS
3.1 Regulatory Strategy. The Parties shall work together through the JDC
and the JMC to determine regulatory strategy in the Territory.
3.2 Regulatory Responsibility in General
(a) AGIX's Responsibilities
(i) AGIX shall be responsible for the preparation, submission,
and maintenance of Regulatory Materials, including without limitation the NDA,
for the First Product in the United States prior to the Assumption Date;
provided, however, that AstraZeneca shall cooperate and assist AGIX as
reasonably requested by AGIX.
(ii) Promptly after the Assumption Date, AGIX shall assign to
AstraZeneca all of AGIX's rights in and to all Regulatory Materials relating to
the First Product, and shall take all other necessary actions required to allow
AstraZeneca to assume ownership, possession and control of such Regulatory
Materials.
(b) AstraZeneca's Responsibilities
(i) After the date of assignment described in Section
3.2(a)(ii), AstraZeneca shall be responsible for the preparation, submission and
maintenance of Regulatory Materials for the First Product in the United States.
(ii) AstraZeneca shall, to the extent set forth in the
Development Plan, be responsible for the preparation, submission and maintenance
of Regulatory Materials for the First Product in all countries outside of the
United States.
(iii) AstraZeneca shall, to the extent set forth in the
Development Plan, be responsible for the preparation, submission and maintenance
of Regulatory Materials for all other Products in the Territory.
(c) Accelerated Assumption Payment
(i) Notwithstanding anything herein to the contrary, at any
time following payment by AstraZeneca to AGIX of the ARISE Milestone and the NDA
Acceptance Milestone and prior to U.S. NDA Approval for the First Product,
AstraZeneca may elect to pay to AGIX a nonrefundable, noncreditable payment of
U.S. [****] (the "ACCELERATED ASSUMPTION PAYMENT"), and thereby (A) become the
owner of
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[****] indicates that certain confidential information contained in this
document has been omitted pursuant to a request for confidential treatment and
filed separately with the Securities and Exchange Commission.
20
the Regulatory Materials in the United States for the First Product in lieu of
AGIX, and (B) assume decision-making authority and responsibility for the
preparation, submission and maintenance of Regulatory Materials and for
interaction with Regulatory Authorities, with the JDC oversight as set forth in
Section 6.3(b) and in accordance with the Development Plan, for any decisions
concerning the First Product. Notwithstanding the foregoing, if Regulatory
Approval for the First Product has not occurred within one hundred eighty (180)
days of the Accelerated Assumption Payment, the Parties shall accept the label
then proposed by the FDA for Regulatory Approval, so as to allow the Parties to
promptly obtain U.S. NDA Approval for the First Product.
(ii) If AstraZeneca makes the Accelerated Assumption Payment,
AstraZeneca shall not be obligated to pay the U.S. NDA Approval Milestone.
(d) Expenses
(i) AGIX's Expenses. Prior to the Assumption Date, AGIX shall
be responsible for the cost of preparing, submitting and maintaining the
Regulatory Materials for the First Product in the United States.
(ii) AstraZeneca's Expenses. AstraZeneca shall be responsible
for the cost of preparing, submitting and maintaining the Regulatory Materials
for (i) the First Product (a) in the United States after the Assumption Date,
and (b) in all of the other countries other than the United States in the
Territory and (ii) for all other Product(s) in the Territory.
(iii) Cooperation Expenses. Each Party shall bear its own
expenses incurred in cooperating with the owner of the Regulatory Materials or
participating in the preparation, submission and maintenance of Regulatory
Materials pursuant to this Section 3.2.
(e) Ownership
(i) Prior to the Assumption Date, AGIX shall own all
Regulatory Materials and any applications and other filings made with the FDA
relating to the First Product.
(ii) Promptly after the Assumption Date as the Parties agree
is appropriate, but no later than promptly after the date of U.S. NDA Approval,
AstraZeneca shall own all Regulatory Materials and any applications and other
filings made with the FDA relating to the First Product.
(iii) AstraZeneca shall own all Regulatory Materials and any
applications and other filings made with a Regulatory Authority relating to the
First Product in all countries other than the United States in the Territory.
Prior to the transfer of ownership of the Regulatory Materials to AstraZeneca as
described in
21
Section 3.2(e)(ii), AGIX shall provide a right of reference to the Regulatory
Materials and shall take all action necessary to effect such right of reference,
to the extent necessary or useful for AstraZeneca to pursue Regulatory Approval
of Products in countries other than the United States.
(iv) AstraZeneca shall own all Regulatory Materials and any
applications and other filings made with a Regulatory Authority relating to any
other Product(s) in the Territory.
(v) Notwithstanding anything in this Agreement to the
contrary:
(A) AGIX may keep archival copies of all Regulatory
Materials that AGIX creates or receives during the Term;
(B) AstraZeneca shall provide to AGIX promptly after
their creation, and AGIX may keep, archival copies of any material
Regulatory Materials (as agreed upon by the Parties) created subsequent to
the Assumption Date, or in connection with Regulatory Materials created or
received by or on behalf of AstraZeneca pursuant to this Agreement at any
time during the Term, including without limitation Section 3.2(e)(i)-(iv);
(C) AGIX shall have the right to use Regulatory
Materials (including study protocols, study results, analytical
methodologies, bulk and final product manufacturing process descriptions,
batch records, vendor qualifications, validation documentation, and
regulatory documentation) for its own internal use in connection with its
research, development and commercialization activities consistent with the
requirements of this Agreement but shall remain obligated under Section 10
with respect to such Regulatory Materials.
(f) Periodic Updates. The owner of the Regulatory Materials shall be
exclusively responsible (with reasonable cooperation from the other Party as may
be requested by the owner of the Regulatory Materials from time to time) for all
post-approval updates to Regulatory Materials, such as annual updates,
supplements and amendments and routine maintenance of the submissions of the
Regulatory Materials that must be provided on a Product at periodic intervals to
the Regulatory Authorities. In addition, the owner of the Regulatory Materials
shall be the sponsor of all filings for Indications.
(g) Relationship with Regulatory Authorities. The Party who owns the
Regulatory Materials shall have primary responsibility for interacting with
Regulatory Authorities, chairing meetings with such Regulatory Authorities,
responding to inquiries of such Regulatory Authorities, and other communications
with such Regulatory Authorities, with regard to such Regulatory Materials or a
Product, including but not
22
limited to, Regulatory Materials related to Indications and Drug Devices. Each
Party shall provide to the other Party copies of any material Regulatory
Materials (and any updates thereto and any other Regulatory Materials reasonably
requested by a Party) submitted to Regulatory Authorities, within five (5) days
of such Party's submission thereof to such Regulatory Authorities .
3.3 Regulatory Authority Communications and Cooperation Between the Parties
(a) General. Each Party shall provide the other Party with a copy of
all material correspondence received from a Regulatory Authority (and any other
correspondence reasonably requested by a Party). Each Party shall consult and
cooperate with the other Party in the preparation of its Regulatory Materials
and any meetings or other correspondence with a Regulatory Authority. Each Party
shall further consult with and keep the other Party regularly and fully informed
of, the preparation, Regulatory Authority review and approval of NDA filings for
which such Party is responsible. Each Party agrees to consider in good faith any
comments or suggestions made by the other Party in relation to any Regulatory
Materials, but the Party responsible for submitting such Regulatory Materials
shall have the final authority to determine the content of such Regulatory
Materials. In the event a Party is meeting in person or by telephone with or has
a hearing before any Regulatory Authority, such Party shall provide the other
Party with reasonable advance notice of the time and date of such meeting or
hearing and any preparatory material for use in such meeting or hearing and a
reasonable number of representatives of the other Party shall have the right to
attend such hearing or meeting.
(b) Communications With Regulatory Authorities. Except as otherwise
provided in the Development Plan, the Party that does not own any particular
Regulatory Materials shall not, without the prior consultation with, and
agreement of the owner of the Regulatory Materials, or unless so required by
law, correspond or communicate with Regulatory Authorities concerning a Product
covered by such Regulatory Materials or any Regulatory Materials related
thereto. Each Party shall keep the other Party informed of notification of any
action by, or notification or other information which it receives (directly or
indirectly) from any Regulatory Authority which: (i) raises any material
concerns regarding the safety or efficacy of a Product; (ii) indicates or
suggests a potential material liability for either Party to third parties
arising in connection with a Product; (iii) is reasonably likely to lead to a
recall or market withdrawal of a Product; (iv) relates to a Product, Regulatory
Materials, Promotional Materials, samples, package inserts, the Indications,
labeling, expedited and periodic Adverse Event Reports, medical inquiries,
Product Complaints, this Agreement or the Related Agreements, or (v) is
otherwise important to the Development and/or Commercialization of the Product.
(c) Communications from Regulatory Authorities. In the event that a
Party receives any communication or questions from any Regulatory Authority,
such
23
Party shall promptly notify the other Party. The owner of the Regulatory
Materials shall then prepare the response to the communication (except for
responses to FDA communications regarding a loss, theft, or significant loss of
the other Party's Product samples). Before submitting a response to a Regulatory
Authority regarding correspondence received by a Party, the owner of the
Regulatory Materials shall give the other Party a reasonable and timely
opportunity to comment on the response to the extent such response may affect
the other Party's rights or obligations under this Agreement. If it is necessary
for such other Party to respond to the FDA or any other Regulatory Authority,
such Party shall seek the input and approval of the owner of the Regulatory
Materials before responding.
(d) Audit by Regulatory Authority. If a Regulatory Authority desires
to conduct an inspection or audit of AstraZeneca or AGIX with regard to a
Product or this Agreement, AstraZeneca and AGIX each agrees to cooperate with
the Regulatory Authority and the other Party during such inspection or audit,
including by allowing, to the extent practicable, a representative of the other
Party to be present during the applicable portions of such inspection or audit.
In the event a Party receives notice that a Regulatory Authority intends to
conduct such an inspection or audit, such Party shall promptly notify the other
Party of receipt of such notice.
3.4 Communications Concerning Product. The Parties shall mutually agree
upon procedures for communication and handling of Product Complaints and medical
inquiries concerning a Product. All Product Complaints concerning suspected or
actual Product tampering, contamination or mix-up (e.g. wrong ingredients) shall
be notified to the owner of the Regulatory Materials by telephone immediately
and delivered in writing within twenty-four (24) hours of receipt of the same.
Except as mutually agreed, the other Party shall not take any other action in
connection with any such Product Complaint without the consent of the owner of
the Regulatory Materials.
3.5 Records. Each Party shall maintain records, in sufficient detail and
in appropriate good scientific manner, that shall fully and properly reflect all
work done and results achieved in the performance of its activities under the
Development Plan and the Commercialization Plan. Each Party shall have the
right, during normal business hours and upon reasonable prior notice, to inspect
those records of the other Party referred to herein that are necessary or useful
to the inspecting Party for any appropriate purpose under this Agreement,
including for the purposes of making any required filings with Regulatory
Authorities in order to obtain Manufacturing approvals and/or Regulatory
Approvals. Each Party shall have the right to copy any such records to the
extent such Party is required to have a copy to comply with Applicable Laws.
Each Party shall maintain such records and the information disclosed therein in
confidence in accordance with Section 10.1.
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3.6 Safety Matters
(a) Information. Until the Assumption Date, AGIX shall provide
AstraZeneca with all information necessary or desirable for AstraZeneca to
comply with all Applicable Laws with respect to the Compounds and the Products,
as the case may be. In furtherance thereof, AGIX shall (a) develop appropriate
adverse experience reporting procedures, (b) provide to AstraZeneca any material
information on the Compounds or Products from preclinical or clinical
laboratory, animal toxicology and pharmacology studies, as well as serious or
unexpected adverse experience reports from clinical trials and commercial
experiences with the Compounds or Products, and (c) report and provide such
information to AstraZeneca in such a manner and time so as to enable AstraZeneca
to comply with all Applicable Law in countries for which Regulatory Approval is
or will be sought or in which the Product is being developed, marketed or sold.
(b) Records and Notice. Until the Assumption Date, AGIX shall (a)
maintain a record of any and all complaints it receives with respect to the
Compounds of the Products, (b) notify AstraZeneca in reasonable detail or any
complaint received by it within ten (10) days after the event, and in any event
in sufficient time to allow AstraZeneca to comply with all Applicable Law in any
country in which the Product is being developed, marketed or sold.
(c) Safety Agreement. The Parties shall, unless both Parties
otherwise agree, after the Execution Date but before the Assumption Date,
negotiate and execute a Safety Agreement containing appropriate provisions
addressing safety issues relating to Products which is consistent with the terms
of this Agreement and the Related Agreements.
4. COMMERCIALIZATION
4.1 Global Commercialization Team and U.S. Commercialization Team. So long
as AGIX is not Developing, Commercializing or Promoting a Competing 1067
Product, AGIX shall be entitled to have up to three (3) representatives
designated by AGIX, at AGIX's expense, attend, observe and participate in
meetings of each of the Global Commercialization Team and U.S. Commercialization
Team having the relevant experience and skill appropriate for service on such
Teams. Such representatives shall be regular working members of the Global
Commercialization Team and U.S. Commercialization Team. AstraZeneca shall
provide AGIX office space at its facilities for such representatives to
facilitate such participation; provided that such representatives shall comply
with all policies and reasonable restrictions imposed by AstraZeneca.
4.2 Commercially Diligent Efforts. AstraZeneca shall use Commercially
Diligent Efforts to Commercialize Product(s) in the Territory as set forth in
Section 5.
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4.3 Commercialization Plan
(a) Commercialization Plan. Within ninety (90) days after the
Effective Date, the Global Commercialization Team shall prepare and provide to
the JMC for the JMC's approval an initial commercialization plan summarizing the
plan for Commercializing the Product given the stage of the Product at the time
of such plan (as such plan may be updated pursuant to Section 4.3(c), the
"COMMERCIALIZATION PLAN"). Promptly following such approval, AstraZeneca shall
implement the activities described in the Commercialization Plan, including, to
the extent set forth in the Commercialization Plan, pre-launch market
development, market research and activities to increase scientific awareness of
the Product.
(b) Content of the Commercialization Plan. An outline of the
anticipated principal components of the Commercialization Plan is included in a
letter delivered by AGIX to AstraZeneca on the date hereof. The
Commercialization Plan as approved by the JMC pursuant to Section 4.3(a), and as
updated from time to time pursuant to Section 4.3(c), shall include, at a
minimum, the items listed in such Commercialization Plan outline, unless the
Parties otherwise agree. Upon adoption, the Commercialization Plan shall
describe the overall plan for Commercializing each Product during the first
three years after Product Launch of such Product in (i) each of the countries in
the Major Markets, (ii) the Secondary Market, and (iii) other countries in the
Territory to the extent applicable. The Commercialization Plan shall include for
each Product, without limitation, (A) a comprehensive marketing, sales, pricing,
distribution and licensing strategy for such Product, including market research
and activities to increase scientific awareness of the Product and
pharmacoeconomic activities and programs to support pricing of the Product; (B)
estimated date of Product Launch, market and sales forecasts, in numbers of
patients and local currency, and competitive analysis for such Product; and (C)
production and inventory forecasts. The Commercialization Plan shall include a
budget which shall detail the levels of spending for all Commercialization
activities covered by the Commercialization Plan and the allocation of projected
sales support and time such sales support shall be spending on the
Commercialization of each such Product.
(c) Updates to the Commercialization Plan. At least once per
Calendar Year, the Global Commercialization Team shall prepare an updated
Commercialization Plan, which shall cover the ensuing three Calendar Years. The
Global Commercialization Team shall provide all such updated Commercialization
Plans to the JMC for review and approval.
4.4 Commercialization Activities of the Parties
(a) Compliance with the Commercialization Plan. The Parties agree to
carry out their activities under the Commercialization Plan.
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(b) AstraZeneca Activities. AstraZeneca shall be responsible for the
distribution and Commercialization of each Product in the Territory, subject to
the terms and conditions of the Co-Promotion Agreement which provides for AGIX's
rights to co-promote Product(s) in the United States.
(c) AGIX Co-Promotion Activities. AGIX shall have the right to
co-promote Product(s) and certain other products in the United States in
accordance with the Co-Promotion Agreement; provided, however, that AGIX shall
only use Promotional Materials supplied to AGIX by AstraZeneca to promote
Product(s).
(d) Commercialization Costs. Except as provided in the Co-Promotion
Agreement, AstraZeneca shall bear all costs for the Commercialization of
Product(s) in the Territory, including pre-approval and market development
activities.
(e) Pricing Decisions. AstraZeneca shall have sole responsibility
for setting pricing for all Product(s), provided that the initial pricing for
any Product(s) shall be subject to JMC approval.
(f) Booking Sales. AstraZeneca (and, as appropriate, its Affiliates
and Sublicensees) shall record on its books all sales of Products worldwide.
4.5 Commercial Manufacturing and Supply of Products
(a) Supply of Compound in Spray Dried Form. The Manufacture and
supply of the active pharmaceutical ingredient in a spray dried form shall be
effected in accordance with the Transition Services Agreement.
(b) Management. Subject to the terms of the Transition Services
Agreement, the JMC shall oversee Manufacturing pursuant to the Development Plan
and the Commercialization Plan.
(c) Product Packaging, Labeling and Formulation. AstraZeneca shall
be solely responsible, at its sole cost, for supplying all of the requirements
of Product formulation, packaging and labeling. AGIX shall use Commercially
Diligent Efforts to facilitate any necessary transfer of technology to
AstraZeneca or a Third Party chosen by AstraZeneca for Product formulation,
packaging and labeling.
5. DILIGENCE AND COOPERATION
5.1 Information Sharing
(a) Cooperation. The Parties agree to fully cooperate in sharing
information regarding Development and Commercialization, including
Manufacturing, of Products in order to keep each Party informed of material
developments and to provide
27
each Party with necessary information (including without limitation any decision
not to pursue Commercialization of Products in a particular country as
contemplated by the Commercialization Plan) for each Party to make decisions in
the manner set forth in this Agreement on material issues as they arise.
(b) Technology Transfer. Each Party agrees to use Commercially
Diligent Efforts to facilitate any necessary transfer of technology to the other
Party, as reasonably requested by such other Party, to support the Development
and Commercialization of Products as contemplated by this Agreement.
5.2 Diligence Requirements
(a) Product Development. Each Party shall use Commercially Diligent
Efforts to conduct Development of Product(s) in accordance with the Development
Plan. Each Party shall conduct its portion of the Development Program, in a good
scientific manner and in compliance in all material respects with all
requirements of Applicable Laws, including cGCPs, cGLPs and cGMPs, to Develop
Products as provided in the Development Plan. Each Party shall use Commercially
Diligent Efforts to provide the other Party with all reasonable assistance and
take all actions reasonably requested by that Party, without changing the
allocation of responsibilities assigned in the Development Plan or this
Agreement, that are necessary or desirable to enable each Party to comply with
the terms and intent of this Agreement. Each Party shall use Commercially
Diligent Efforts to assist the other Party, as provided in the Development Plan,
to conduct Development of and obtain Regulatory Approvals of Products.
(b) Commercialization
(i) AstraZeneca shall, itself or through its permitted
Sublicensees, use Commercially Diligent Efforts to Commercialize Products in
each Major Market.
(ii) AstraZeneca shall, itself or through its Sublicensees,
use Commercially Diligent Efforts to Commercialize Products in the Secondary
Market. All of the countries comprising the Secondary Market shall for this
purpose be considered together as one market as a whole. The level of
Commercially Diligent Efforts made in the Secondary Market shall take into
consideration the total commercial potential of Products in the Secondary Market
taken as a whole.
(iii) Each Party shall conduct its portion of the
Commercialization Plan in compliance in all material respects with all
requirements of Applicable Laws.
(c) Coated Stents. AstraZeneca shall, itself or through its
permitted Sublicensees, use Commercially Diligent Efforts to Develop and
Commercialize a
28
Coated Stent in the United States if, after the first U.S. NDA Approval, the JMC
approves Development of a Coated Stent. AstraZeneca shall not have any other
obligation to use Commercially Diligent Efforts (or any other level of efforts)
to Develop or Commercialize a Coated Stent prior to any such approval, or in any
jurisdiction outside the United States.
5.3 Failure To Use Diligence
(a) Notice of Failure. If AGIX believes that AstraZeneca is failing
to satisfy its obligations to use Commercially Diligent Efforts in accordance
with this Section 5, AGIX may give AstraZeneca notice of such alleged failure,
which notice shall describe such failure with reasonable specificity.
(b) AstraZeneca Response. Within thirty (30) days following
AstraZeneca's receipt of any such notice from AGIX, AstraZeneca shall provide
AGIX with a written response specifying, in reasonable detail, whether or not it
agrees with AGIX's belief and the reasons for its disagreement, if applicable.
(c) Disputes. In the event of a dispute between the Parties with
respect to whether AstraZeneca is using its Commercially Diligent Efforts in
accordance with Section 5, as evidenced by notice from AstraZeneca of a
disagreement pursuant to Section 5.3(b), such dispute shall be resolved in
accordance with Section 14. Neither Party may initiate dispute resolution under
Section 14 until sixty (60) days after receipt by AGIX of a notice of
disagreement described in Section 5.3(b).
6. GOVERNANCE
6.1 General. The activities of the Parties pursuant to this Agreement
shall be governed by the Alliance Managers, the JMC, the JDC, the IPC and such
additional committees as established by the JMC, as provided in this Section 6.
6.2 Alliance Managers
(a) Appointment and Roles. Promptly after the Effective Date, each
of the Parties shall appoint a single individual to act as that Party's alliance
manager (the "ALLIANCE MANAGER"). The role of the Alliance Managers is to
facilitate the relationship between the Parties. Alliance Managers may attend
JMC meetings, JDC meetings and any other meetings of additional committees or
subgroups established by the JMC pursuant to Section 6.1 and shall support the
chairpersons of each such committee and group in the discharge of their
responsibilities. Alliance Managers shall be nonvoting participants in such
Committee meetings, unless they are also appointed members of such Committee.
Each Party's Alliance Manager shall alternate serving as the secretary to the
JMC on an annual basis, starting with AGIX.
29
(b) Availability of Facilities. Each Party shall allow the other
Party's Alliance Manager to spend any amount of time at the other Party's
offices as is necessary for the other Party to perform its activities under this
Agreement; provided that, each Alliance Manager shall comply with all policies
and reasonable restrictions imposed by the Party hosting such Alliance Manager.
(c) Changes in Alliance Managers. Each Party may change its
designated Alliance Manager from time to time upon written notice to the other
Party.
6.3 Committees
(a) JMC
(i) Formation and Duration. No later than thirty (30) days
after the Effective Date, the Parties shall establish a Joint Management
Committee ("JMC").
(ii) Activities of the JMC. The JMC shall be responsible for
overall strategic and operational direction of the Collaboration, including
without limitation:
(A) developing and implementing accountability
mechanisms for the JDC, IPC and any other committees formed under this
Agreement;
(B) overseeing the Manufacture of Product for commercial
sales;
(C) reviewing and approving the Commercialization Plan
and Development Plan and any amendments thereto;
(D) making decisions regarding Development for
Indications and Combination Products and any Coated Stent or other Drug
Device following the first Regulatory Approval of the first Product
(however, the JMC will consider and plan, but not decide, such activities
prior to such Regulatory Approval); provided that, the JMC shall have no
obligation to approve Development for Combination Products that include
Exclusive Market Products;
(E) establishing additional committees or subgroups as
the JMC deems necessary or appropriate; and
(F) Product life cycle management relating to the
Products.
30
(iii) Composition. Each Party shall designate up to four (4)
representatives and a nonvoting Alliance Manager for membership on the JMC
having the relevant experience and skill appropriate for service on the JMC.
(iv) Meetings. During the Term and unless otherwise agreed to
by the Parties, the JMC shall meet a minimum of four times each Calendar Year in
accordance with a schedule determined by the Parties and to be held in Atlanta,
Georgia or Puerto Rico, unless the Parties otherwise mutually agree. Additional
ad hoc meetings of the JMC may be called by either Party upon reasonable advance
notice to the other Party. A Party may attend any meeting of the JMC by
teleconference, video or Webex.
(b) JDC
(i) Formation and Duration. No later than thirty (30) days
after the Effective Date, the Parties shall establish a Joint Development
Committee ("JDC").
(ii) Activities of the JDC. The JDC shall be responsible for
oversight of all Development, including without limitation the following:
(A) clinical trials (including Phase IV trials) of a
Product;
(B) preparing for approval by the JMC the Development
Plans and the budgets of Development Costs and overseeing the
implementation thereof ;
(C) proposing updates and amendments to the Development
Plan for approval by the JMC;
(D) reviewing protocols for clinical studies of a
Product;
(E) reviewing and overseeing regulatory strategies for
each Product
(F) reviewing and approving the final Statistical
Analysis Plan; and
(G) reviewing, prior to its submission to the Third
Party statistician of the ARISE Study, the ARISE Results.
(iii) Composition. AGIX shall designate three (3)
representatives and AstraZeneca shall designate three (3) representatives for
membership on the JDC having the relevant experience and skill appropriate for
service on the JDC.
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(iv) Meetings. Prior to U.S. NDA Approval for the First
Product, the JDC shall meet at least once a month. After U.S. NDA Approval and
unless otherwise agreed to by the Parties, the JDC shall meet at least four
times each Calendar Year. Such meetings shall be in accordance with a schedule
and at a location mutually determined by the Parties. Ad hoc meetings of the JDC
may be called by either Party upon reasonable advance notice to the other Party.
Upon mutual agreement, such ad hoc meetings may be face-to-face or by
teleconference, video or Webex.
(c) Representatives. The Parties, through the committee structure,
may establish and later change the number of representatives on the JMC or JDC
committee as long as an equal number of representatives from each of AstraZeneca
and AGIX are maintained. Each Party may change its representatives to the JDC or
JMC at any time by written notice to the other Party.
(d) Committee Chairs. The JMC shall be co-chaired by AstraZeneca and
AGIX. Prior to the earlier of (a) the date U.S. NDA Approval is received and (b)
the date that AstraZeneca makes an Accelerated Assumption Payment, the JDC shall
be chaired by a representative of AGIX. After such date, the JDC shall each be
chaired by a representative of AstraZeneca.
(e) Expenses. Each Party shall bear the expense of the participation
of its respective members and the Alliance Managers in the JMC and JDC meetings.
(f) Agenda and Minutes. At least five (5) Business Days prior to
each JDC or JMC meeting, each Party shall provide written notice to the other
Party of agenda items proposed by such Party for discussion or decision at such
meeting, together with appropriate information related thereto. At least two (2)
Business Days prior to each JDC or JMC meeting, each Party shall provide written
copies to the other Party of all presentations to be made at such meeting.
Reasonably detailed written minutes shall be kept of all JDC and JMC meetings
and shall reflect, without limitation, material decisions made at such meeting.
Responsibility for keeping the JMC minutes shall alternate between the co-chairs
of each Party, beginning with AstraZeneca. The chairperson of the JDC shall be
responsible for keeping the JDC minutes. Meeting minutes shall be sent to each
committee member for review and approval within five (5) Business Days after
such meeting. Minutes shall be deemed approved unless a committee member objects
to the accuracy of such minutes within ten (10) Business Days of receipt.
(g) Decision-making
(i) Decisions. The Parties' representatives on the JMC and JDC
shall use all reasonable efforts, acting in good faith, to resolve all issues
presented to them as expeditiously as possible. Each Party's representatives on
the JMC and JDC shall make decisions by consensus. All JMC and JDC decisions
shall be made by unanimous vote, and each Party's representatives shall
collectively have one vote.
32
(ii) Decision-making Authority. Notwithstanding anything to
the contrary, neither the JDC or the JMC shall have the authority to determine
any of the matters for which (i) one or more of the Parties is allocated
decision-making authority elsewhere in this Agreement or (ii) the Agreement
provides that the matter in question is explicitly a matter requiring the mutual
or joint agreement of the Parties. Each of the JDC and JMC shall be deemed to
have a quorum if they have at least two (2) designated representatives from each
Party. A quorum shall also be deemed to have been achieved if at least ten (10)
Business Days written notice of a meeting, including a proposed agenda, has been
provided for a meeting held by telephone conference or in Atlanta, Georgia or
Puerto Rico.
(iii) Disputes
(A) JDC Disputes. The JDC, or either Party, may, after
thirty (30) days (or such other period as the Parties otherwise agree) of
good faith efforts to reach a unanimous decision on an issue, refer any
unresolved issue to the respective heads of the appropriate department for
each Party. If the department heads can not resolve such issue within ten
(10) days, then such issue shall be referred to the JMC.
(B) JMC Disputes. The JMC or either Party may, after
thirty (30) days (or such other period as the Parties may otherwise agree)
of good faith efforts to reach a unanimous decision on an issue refer such
issue to the officers set forth in Section 14.1(b), or their designee.
Such officers of the Parties shall meet promptly thereafter and shall
negotiate in good faith to resolve the issues. If the issues were raised
by the JDC and if they cannot resolve the issue within thirty (30) days of
commencing negotiations, prior to the earlier of (i) the date U.S. NDA
Approval is received and (ii) the date upon which AstraZeneca makes an
Accelerated Assumption Payment, the resolution of such issue shall be
determined by AGIX. For all other JMC issues, the resolution of any such
issue shall be determined by AstraZeneca.
(iv) Decisions Affecting Development and Commercialization
Plans. Notwithstanding anything in this Section 6 to the contrary:
(A) no decision by the JDC or the JMC shall affect
AstraZeneca's control of all aspects regarding the Commercialization of
Products;
(B) neither Party's rights and obligations as contained
in this Agreement can be amended without such Party's consent;
(C) prior to the Assumption Date, no decision by the JDC
or the JMC shall increase AstraZeneca's development obligations as set
forth in the Development Plan Outline or AstraZeneca's commercialization
obligations
33
as set forth in the Commercialization Plan outline included in a letter
delivered by AGIX to AstraZeneca on the date hereof, without the consent
of AstraZeneca; and
(D) after the Assumption Date, AstraZeneca shall have
authority to determine the resolution of any disagreement in the JMC with
respect to the approval of the Development Plan governing activities
following U.S. NDA Approval, even if such Development Plan was approved
prior to U.S. NDA Approval.
(h) IPC. No later than thirty (30) days after the Effective Date,
the Parties shall establish an Intellectual Property Committee ("IPC"). The IPC
shall be responsible for overseeing all intellectual property matters as further
described in Section 9. The IPC shall be governed by the rules and procedures
set forth in Section 9.2.
7. LICENSES AND COVENANTS
7.1 License Grants to AstraZeneca
(a) License to AGIX IP. Subject to the terms of this Agreement,
including Section 7.1(b) and Section 7.1(c), and AGIX's retained rights solely
to the extent necessary to perform it obligations under the Transition Services
Agreement, AGIX hereby grants to AstraZeneca an exclusive license, with the
right to sublicense, under the AGIX Compound Patents, Other AGIX Patents and
AGIX Know-How (other than as set forth in Exhibit 11.5), to research, develop,
make, have made, use, sell, have sold, offer for sale and import the Compound
and Products in the Field in the Territory.
(b) Distribution and Co-Promotion
(i) Neither AstraZeneca nor its Affiliates shall be permitted
to appoint distributors to distribute, market or sell Products in any Major
Market [****] without the prior approval of AGIX.
(ii) AstraZeneca and its Affiliates shall have the right, in
their sole discretion, to appoint distributors to distribute, market and sell
the Products [****] and in any other countries in the Territory that are not
part of the Major Market.
(iii) AstraZeneca and its Affiliates shall have the right, in
their sole discretion, to co-promote the Products with Third Parties in
countries other than the Major Market and to appoint Third Parties to promote
the Products in such countries.
(iv) Notwithstanding the foregoing, AstraZeneca may appoint
any Affiliate to distribute, market or sell Products without restriction.
-------
[****] indicates that certain confidential information contained in this
document has been omitted pursuant to a request for confidential treatment and
filed separately with the Securities and Exchange Commission.
34
(v) Notwithstanding anything herein to the contrary,
AstraZeneca may engage contract sales organizations to Promote Products,
provided that any sales of Products effected by any such organization are booked
by AstraZeneca.
(c) Sublicenses
(i) Neither AstraZeneca nor its Affiliates shall be permitted
to enter into any Noncompulsory Sublicenses in any Major Market [****] without
the prior approval of AGIX.
(ii) AstraZeneca and its Affiliates shall be permitted to
enter into Compulsory Sublicenses and Noncompulsory Sublicenses in any country
in the Territory other than a Major Market on the terms set forth in this
Section 7.1(c).
(iii) AstraZeneca and its Affiliates shall not enter into any
Noncompulsory Sublicense of the rights granted in this Agreement with a
Sublicensee to the extent permitted in this Section 7.1(c) unless the
Sublicensee agrees to all applicable terms of this Agreement.
(iv) No Compulsory Sublicenses or Noncompulsory Sublicense
shall relieve AstraZeneca of any obligations it has under this Agreement.
(v) AstraZeneca shall promptly notify AGIX upon entering into
any Compulsory Sublicense and any Noncompulsory Sublicense.
(vi) Notwithstanding the foregoing, AstraZeneca may enter into
any Sublicense with any Affiliate without restriction, except as described in
clauses (iii) and (iv) of this Section 7.1(c).
(vii) All Sublicensees shall be bound by the provisions of
Section 10 of this Agreement.
7.2 License Grants to AGIX. Subject to the terms and conditions of this
Agreement, AstraZeneca hereby grants to AGIX a non-exclusive, royalty-free
license, with the right to sublicense, under AstraZeneca IP and AGIX IP, to
Develop, Manufacture and Commercialize the Compound and Products in the Field
only to the extent necessary for AGIX to perform its obligations and exercise
its rights under this Agreement and the Transition Services Agreement. AGIX
shall promptly notify AstraZeneca upon entering into any sublicense under this
Section 7.2. All such sublicensees shall be bound by the provisions of Section
10 of this Agreement.
7.3 Rights Acquired from Third Parties
(a) Option. In the event that AGIX acquires or licenses, or has the
opportunity to acquire or license, rights from any Third Party (other than the
Pre-Existing
-------
[****] indicates that certain confidential information contained in this
document has been omitted pursuant to a request for confidential treatment and
filed separately with the Securities and Exchange Commission.
35
Third Party Licenses) that, if Controlled by AGIX would be Licensed Patents or
AGIX Know-How, and where AGIX is required to pay upfront payments, royalties,
milestones or other payments to such Third Party for such rights, then:
(i) AGIX shall send AstraZeneca a written notice within thirty
(30) days of when AGIX has licensed or otherwise acquired such rights;
(ii) AstraZeneca shall have the option to acquire a
Non-Exclusive Sublicense to such rights to Develop, Manufacture and
Commercialize the Compound and Products in the Field during the Term from any
Party where AGIX is required to pay royalties, milestones or other payments
(including upfront payments) to such Third Party for such rights (to the extent
that such Third Party permits such Sublicense to be granted to AstraZeneca);
provided that AstraZeneca reimburses AGIX for a portion of the amounts paid by
AGIX to such Third Party that are reasonably allocable to AstraZeneca as agreed
to by the Parties based on the value to AstraZeneca of such Sublicense relative
to its use by AGIX and Third Parties for other purposes; and
(iii) The option described in this Section 7.3 may be
exercised by written notice to AGIX at any time within sixty (60) days after
receipt of the written notice described in Section 7.3(a)(i), which shall be
accompanied by an undertaking by AstraZeneca to pay to AGIX the payments
required by this Section 7.3.
(b) Participation in Discussion with Third Parties. To the extent
practicable and permitted, if AGIX identifies any rights described in Section
7.3(a) that are controlled by a Third Party and that were developed
independently of AGIX and where AGIX is considering acquiring such rights solely
for use in Development and Commercialization of the Compound and Products, AGIX
shall permit AstraZeneca to participate in any discussions with such Third Party
regarding obtaining a Sublicense to any such rights.
7.4 Covenants Concerning the Products, the Compound and the Field
(a) Expansion of Field for the Compound. In the event that AGIX can
reasonably demonstrate that the exploitation of the Compound in an indication
outside of the Field (the "EXPANDED FIELD INDICATION") presents a reasonable
commercial opportunity, then AGIX may, but shall not be required to, present to
AstraZeneca all relevant information demonstrating such opportunity for the
Compound in the Expanded Field Indication (the "INDICATION INFORMATION"). Any
dispute regarding whether an Expanded Field Indication presents reasonable
commercial opportunity shall be resolved in accordance with Section 14 of this
Agreement. For the [****] Expanded Field Indications, within thirty (30)
days of receipt of the Indication Information, (i) AstraZeneca shall pay to AGIX
[****] and (ii) the Field shall automatically be expanded to include the
Expanded Field Indication. Following the [****] payments of the Indication
Fee as described in the preceding sentence, upon delivery of Indication
Information regarding additional Expanded Field Indications, the
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[****] indicates that certain confidential information contained in this
document has been omitted pursuant to a request for confidential treatment and
filed separately with the Securities and Exchange Commission.
36
Field shall automatically be expanded to include such Expanded Field
Indications, but no further Indication Fees shall be due to AGIX. AstraZeneca
shall be free to Develop, Commercialize and Manufacture, in its discretion, the
Compound and any Product within any Expanded Field Indication. The provisions of
Articles 2, 3, 4, 5, 6 and Sections 8.1, 8.2 shall not apply to any Development,
Manufacture or Commercialization of a Product within the Expanded Field
Indication. AGIX shall not directly or indirectly Develop, Commercialize or
Manufacture the Compound other than pursuant to this Agreement.
(b) Expansion of Field for Probucol Analogs. In the event that AGIX
can reasonably demonstrate that the exploitation of a Probucol Analog in the
Field (the "LICENSED PROBUCOL ANALOG") presents a reasonable commercial
opportunity, then AGIX may, but shall not be required to, present to AstraZeneca
all relevant information demonstrating such opportunity for such Licensed
Probucol Analog (the "PROBUCOL ANALOG INFORMATION"). Any dispute regarding
whether an Licensed Probucol Analog presents reasonable commercial opportunity
shall be resolved in accordance with Section 14 of this Agreement. For the
[****] Licensed Probucol Analogs, within thirty (30) days of receipt of the
Indication Information, (i) AstraZeneca shall pay to AGIX [****] and (ii) the
definition of Compound under this Agreement shall automatically be expanded to
include the Licensed Probucol Analog. Following the [****] payments of the
Probucol Analog Fee as described in the preceding sentence, upon delivery of
Probucol Analog Information regarding additional Licensed Probucol Analogs, the
definition of Compound shall automatically be expanded to include such Licensed
Probucol Analogs, but no further Probucol Analog Fee shall be due to AGIX.
AstraZeneca shall be free to Develop, Manufacture and Commercialize, in its
discretion, any Licensed Probucol Analog within the Field. The provisions of
Articles 2, 3, 4, 5, 6 and Sections 8.1, 8.2 shall not apply to any Development,
Manufacture or Commercialization of a Licensed Probucol Analog within the Field.
AGIX shall not directly or indirectly Develop, Manufacture or Commercialize any
Probucol Analog in the Field other than the Development, Manufacture or
Commercialization of Products pursuant to this Agreement and otherwise pursuant
to this Section.
(c) Cooperation
(i) Subject to Section 7.4(c)(iii), AGIX shall consult with
AstraZeneca prior to engaging in any activity that AGIX believes could violate
the requirements of this Section 7.4. As part of such consultation, AGIX shall
provide to AstraZeneca such information as AstraZeneca reasonably requests to
assist AstraZeneca in discussing such activities.
(ii) Subject to Section 7.4(c)(iii), AstraZeneca may at any
time initiate discussions with AGIX if AstraZeneca reasonably believes that AGIX
has been violating or could violate the requirements of this Section 7.4. AGIX
shall provide to AstraZeneca such information as AstraZeneca reasonably believes
is necessary to assist
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[****] indicates that certain confidential information contained in this
document has been omitted pursuant to a request for confidential treatment and
filed separately with the Securities and Exchange Commission.
37
AstraZeneca in considering whether such activities constituted or could
constitute such a violation.
(iii) AGIX may, in lieu of consulting with AstraZeneca
pursuant to Section 7.4(c)(i) or Section 7.4(c)(ii), or in lieu of providing
information pursuant to either such section, elect to seek an opinion from a
neutral outside patent counsel with appropriate legal and technical credentials
as to whether a compound to be developed, manufactured or commercialized by AGIX
is a Probucol Analog in the Field. AGIX shall inform AstraZeneca in writing
promptly upon making any such election. AGIX shall select the neutral outside
patent counsel from the list of appropriate outside patent counsel created by
the IPC pursuant to Section 9.2(c)(i). Such counsel shall not disclose to
AstraZeneca any discussions between AGIX and the counsel, or any other
information provided to such counsel by AGIX. AGIX shall provide to AstraZeneca
a copy of any such opinion, with such opinion to be redacted as AGIX reasonably
considers appropriate to protect AGIX's proprietary interests. In the event such
counsel determines that, in such counsel's opinion, the compound AGIX proposes
to develop, manufacture or commercialize is not a Probucol Analog in the Field,
AGIX shall (assuming its activities otherwise comply with Section 7.4(b)) be
permitted to continue engaging in such activities subject to AstraZeneca's
further right to initiate discussions pursuant to Section 7.4(c)(ii); provided,
however, that to the extent AstraZeneca disagrees with such determination,
AstraZeneca may refer such issue to arbitration in accordance with Section 14.
In the event such counsel determines that, in such counsel's opinion the
compound proposed to be developed, manufacture or commercialized is a Probucol
Analog in the Field, AGIX shall cease such activities promptly; provided,
however, that to the extent that AGIX disagrees with such determination, AGIX
may refer the issue to arbitration in accordance with Section 14. If such
neutral patent counsel determines that such compound is not a Probucol Analog in
the Field and AstraZeneca refers such issue to arbitration pursuant to Section
14, AGIX shall be permitted to continue such activities during the pendency of
such arbitration proceedings.
(d) AGIX Activities Outside this Agreement. AstraZeneca shall not
take any action that would prevent appropriate cardiovascular safety studies on
Probucol Analogs being developed for therapeutic uses outside the Field,
including, but not limited to, preclinical studies and clinical studies such as
Thorough QT Studies or long-term cardiovascular safety studies required by
Regulatory Authorities for clinical development and registration of such
compounds for indications outside the Field; provided that no such study shall
result in a label for a Probucol Analog that would permit a promotable efficacy
claim in the Field.
(e) Equitable Remedies. Each Party acknowledges that its breach of
Section 7.4 would cause the other Party irreparable injury for which it would
not have an adequate remedy at law. In the event of such a breach, the
non-breaching Party shall be entitled to obtain injunctive relief, without the
need to show damages or harm, in addition to any other remedies it may have at
law or in equity.
38
(f) Certain AstraZeneca Actions Involving AGIX Patents. AstraZeneca
shall not (i) directly or indirectly oppose, or assist any Third Party to
oppose, in any patent office or court proceeding, the grant of any patent or
patent application within the Licensed Patents, and, in any patent office or
court proceeding, dispute or directly or indirectly assist any Third Party to
dispute, the validity of any patent within the Licensed Patents or any of the
claims thereof, including opposing any application for amendment thereto; or
(ii) bring any claim or proceedings of whatever nature in relation to the
Licensed Patents against AGIX and AGIX's Affiliates (and in respect of the
foregoing their directors and officers) in respect of any activities carried out
by them under any Licensed Patents which may be the subject of a Valid Patent
Claim of the Licensed Patents; provided, however, that the foregoing shall not
prohibit AstraZeneca from bringing an action against AGIX as the result of any
breach of a representation, warranty, covenant or obligation by AGIX or
Affiliates or otherwise under or arising out of this Agreement.
(g) Non-solicitation. During the Term, neither Party, nor any of its
Affiliates, or Representatives of such Party or Affiliate, shall, in any manner,
directly or indirectly, independently, in concert with a Third Party, or on
behalf of a Third Party, solicit to employ any of the officers or management
employees of the other Party, or of any Affiliate of such other Party, as well
as any employee in such other Party's, or the other Party's Affiliate's,
research department, without in any such case obtaining the prior written
consent of such other Party; provided that nothing herein prevents a Party from
making general solicitations not directed to the other Party's or the other
Party's Affiliate's employees, such as customary advertisements or website
postings.
8. PAYMENTS AND REPORTS
8.1 Upfront Payment. In partial consideration for the licenses and other
rights granted in this Agreement and the Related Agreements, AstraZeneca shall
pay to AGIX a nonrefundable, noncreditable payment of Fifty Million Dollars (US
$50,000,000) within three (3) Business Days following the Effective Date. Such
payment shall be made in immediately available funds via a Federal Reserve
electronic wire transfer to a bank account designated by AGIX.
8.2 Milestone Payments
(a) Timing of Payment
(i) The Parties shall be obligated to pay the milestones
described in this Section 8 upon occurrence of the applicable milestone event
and a notice from the Party that first becomes aware of the event to the other
Party.
39
(ii) The Party obligated to pay the milestone shall have
fifteen (15) days following receipt of each notification of the achievement of a
Development Milestone listed below and the milestone listed in Section 8.2(e) in
which to pay the corresponding amount to the other Party in immediately
available funds via a Federal Reserve electronic wire transfer to an account
designated by such receiving Party.
(iii) Each Commercial Milestone listed below shall be payable
with the Royalty due for the fourth Calendar Quarter of the Calendar Year in
which the Commercial Milestone is met for the first time. If more than one
Commercial Milestone is achieved in any Calendar Year, all Commercial Milestones
due for such Calendar Year shall be payable with the Royalty due for the fourth
Calendar Quarter of the Calendar Year in which the Commercial Milestones are
met.
(b) Disclosure of Development Milestone Obligation. Each Party shall
inform the other Party within five (5) days of the achievement of any such
Development Milestone by such Party, its Affiliate or Sublicensee, and shall
provide the other Party with substantiation of the achievement of the milestone.
(c) No Multiple Milestones. Each Development Milestone and
Commercial Milestone shall be payable one time only and not for each Product or
Indication or for each time that the "Annual Net Sales" (total Net Sales in a
Calendar Year) exceeds a certain amount.
40
(d) Milestones Payable to AGIX
Payment Amount
--------------
Development Milestones
[****]
TOTAL ACHIEVABLE DEVELOPMENT MILESTONES ...................................... $ 300 MILLION
Commercial Milestones
[****]
TOTAL ACHIEVABLE COMMERCIAL MILESTONES .............................. $ 650 MILLION
Notwithstanding the foregoing, the [****] period specified for [****] shall be
tolled (i.e., extended) for an additional period equal to the number of days
between when it is determined that there are Final Arise Results and the date
that AstraZeneca advises AGIX that it has initiated a CMIT Study.
(e) Milestone Payable to AstraZeneca. AGIX shall pay AstraZeneca
[****] upon Product Launch of a Coated Stent in the United States.
8.3 Royalties. AstraZeneca will pay to AGIX Royalties as provided in this
Section 8.3.
(a) Royalties for Sales in [****] During [****]. Except as provided
in Section 8.4, for each of the first three Calendar Quarters of each Calendar
Year during the applicable Royalty Term, AstraZeneca will pay AGIX, no later
than forty-five (45) days following the end of each such Calendar Quarter, the
following Royalties on Net Sales for such Calendar Quarter at the applicable
royalty rates based on Annualized
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[****] indicates that certain confidential information contained in this
document has been omitted pursuant to a request for confidential treatment and
filed separately with the Securities and Exchange Commission.
41
Quarterly Net Sales of all Products sold in the [****], subject to
adjustment in accordance with Section 8.4:
(i) [****] if such Annualized Quarterly Net Sales are less
than or equal to [****];
(ii) [****] if such Annualized Quarterly Net Sales are greater
than [****] and less than or equal to [****];
(iii) [****] if such Annualized Quarterly Net Sales are
greater than [****]and less than or equal to [****];
(iv) [****] if such Annualized Quarterly Net Sales are greater
than [****] and less than or equal to[****];
(v) [****]if such Annualized Quarterly Net Sales are greater
than [****] and less than or equal to [****]; and
(vi) [****]if such Annualized Quarterly Net Sales are greater
than[****] and less than [****].
The percentage rate specified in Sections 8.3(a)(i) through (vi) above shall
apply to all Net Sales and not just Net Sales above the levels specified in each
subsection. For example, if Net Sales in [****] for a Calendar Quarter are
[****], the Royalty payable to AGIX for such sales would be [****].
For Annualized Quarterly Net Sales in [****] in excess of [****], a Royalty
of[****] plus an additional Royalty of [****] of the amount in excess of [****]
shall be paid. Thus, for example, if Net Sales in [****] for a Calendar Quarter
are [****], the Royalty payable to AGIX for such sales would be [****].
(b) Royalties for Sales Outside [****] During [****]. Except as
provided in Section 8.4, for each of the first three Calendar Quarters of each
Calendar Year during the applicable Royalty Term, AstraZeneca will pay AGIX, no
later than forty-five (45) days following the end of each such Calendar Quarter,
the following Royalties on Net Sales for such Calendar Quarter at the applicable
royalty rates based on the aggregate Annualized Quarterly Net Sales of all
Products sold in all countries and jurisdictions in the Territory other than
[****], subject to adjustment in accordance with Section 8.4:
(i) [****] if such Annualized Quarterly Net Sales are less
than or equal to [****];
(ii) [****]if such Annualized Quarterly Net Sales that are
greater than [****]and less than or equal to [****];
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[****] indicates that certain confidential information contained in this
document has been omitted pursuant to a request for confidential treatment and
filed separately with the Securities and Exchange Commission.
42
(iii) [****] if such Annualized Quarterly Net Sales are
greater than [****] and less than or equal to [****]; and
(iv) [****] if such Annualized Quarterly Net Sales are greater
than [****]. The percentage rate specified in Sections 8.2(b)(i) through (iv)
above shall apply to all Net Sales, and not just Net Sales above the levels
specified in each subsection. Thus, for example, if Net Sales in all countries
in the Territory [****] for a Calendar Quarter are [****], the Royalty payable
to AGIX for such sales would be [****].
(c) Royalties Payable for the Fourth Calendar Quarter of Each
Calendar Year. Except as provided in Section 8.4, although Royalties payable for
the first three Calendar Quarters of each Calendar Year are based on Annualized
Quarterly Net Sales pursuant to Section 8.3(a) and Section 8.3(b), total
Royalties for each Calendar Year shall be based on total Net Sales for such
Calendar Year. As the level of Annualized Quarterly Net Sales in each Calendar
Quarter of a given Calendar Year increases or decreases, the Royalty payable for
the fourth Calendar Quarter of such Calendar Year shall be adjusted so that the
total Royalties due for such Calendar Year are paid for total Net Sales for the
entire Calendar Year rather than Annualized Quarterly Sales. Thus,
notwithstanding anything in this Section 8.3 to the contrary, Royalties owed and
paid in respect of the fourth Calendar Quarter of each Calendar Year during the
Term (and in respect of the final Calendar Quarter of the Term if it is not a
fourth Calendar Quarter) shall be determined in accordance with this Section
8.3(c).
(i) First, Royalties owed for Net Sales for the entire
Calendar Year [****]shall be determined as follows, subject to adjustment in
accordance with Sections 8.4:
(A) [****] if such total Net Sales for such Calendar
Year are less than or equal to [****];
(B) [****] if such total Net Sales for such Calendar
Year are greater than [****] and less than or equal to [****];
(C) [****] if such total Net Sales for such Calendar
Year are greater than [****] and less than or equal to [****];
(D) [****] if such total Net Sales for such Calendar
Year are greater than [****]and less than or equal to [****];
(E) [****] if such total Net Sales for such Calendar
Year are greater than [****] and less than or equal to [****];
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[****] indicates that certain confidential information contained in this
document has been omitted pursuant to a request for confidential treatment and
filed separately with the Securities and Exchange Commission.
43
(F) [****] if such total Net Sales for such Calendar
Year are greater than [****] and less than [****].
For total Net Sales for such Calendar Year [****] in excess of [****], a Royalty
of [****] plus an additional Royalty of [****] of the amount in excess of [****]
shall be paid.
(ii) Second, Royalties owed for Net Sales for the entire
Calendar Year for [****] shall be determined as follows, subject to adjustment
in accordance with Section 8.4:
(A) [****] if such total Net Sales for such Calendar
Year are less than or equal to [****];
(B) [****] if such total Net Sales for such Calendar
Year are greater than [****] and less than or equal to [****];
(C) [****]if such total Net Sales for such Calendar Year
are greater than [****] and less than or equal to [****]; and
(D) [****] if such total Net Sales for such Calendar
Year are greater than [****].
(iii) Third, the sums determined pursuant to Section 8.3(c)(i)
and Section 8.3(c)(ii) shall be added together.
(iv) Fourth, the total Royalties paid by AstraZeneca in
respect of the first three Calendar Quarters for such Calendar Year shall be
subtracted from the amount determined pursuant to Section 8.3(c)(iii).
(v) Finally, the Royalty due and payable in respect of the
fourth Quarter of the Calendar Year shall equal the amount determined pursuant
to Section 8.3(c)(iv).
(vi) For example, if total Royalties paid in the first three
Calendar Quarters of a given Calendar Year are [****], and Net Sales for such
Calendar Year [****] are [****] and Net Sales for such Calendar Year for [****]
are [****], and there are no adjustments pursuant to Section 8.4, the Royalty
due for the fourth Calendar Quarter of such Calendar year is [****].
8.4 Adjustments and Changes to Royalty Rates in Certain Circumstances
(a) End of Royalty Term. Notwithstanding anything else to the
contrary in Section 8.3, if, during the applicable Royalty Term in any country
in the Territory, there ceases to be a Valid Patent Claim of a Licensed Patent,
Joint Patent or
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[****] indicates that certain confidential information contained in this
document has been omitted pursuant to a request for confidential treatment and
filed separately with the Securities and Exchange Commission.
44
AstraZeneca Patent that would preclude a Third Party from developing, making,
using, selling or importing such Product in such country, then during the
remainder of the applicable Royalty Term, Royalties payable pursuant to this
Section 8 shall be reduced in such country so that they would equal [****] of
the Royalties that otherwise would have applied during such period in such
country (taking into account all adjustments, including those under subsections
(b) through (f) below), but for this Section 8.4(a). For example, if Net Sales
[****] for the first Calendar Quarter of a particular Calendar Year was [****]
and further assuming that on the day immediately preceding such Calendar Quarter
there ceases to be a Valid Patent Claim of a Licensed Patent, Joint Patent or
AstraZeneca Patent that would preclude a Third Party from developing, making,
using, selling or importing such Product [****], and if the Net Sales [****] for
such first Calendar Quarter was [****] (and further assuming that there were not
other sufficient Net Sales [****] that increased the applicable royalty rate to
more than [****]), then the Royalty payable to AGIX for such sales [****] would
be [****]. Any such Royalties shall be payable at the times and under the
circumstances otherwise provided in this Section 8.
(b) Third Party Royalties
(i) The Royalties required to be paid with respect to any
particular country and any particular Calendar Quarter pursuant to Section 8.3
shall be subject to a reduction by AstraZeneca in an amount equal to [****] of
the amount of Third Party Royalties (other than royalties and other payments
paid pursuant to Pre-Existing Third Party Licenses arising out of the
Development or Commercialization of Products) that were paid by AstraZeneca in
such country during such Quarter to any Third Party that is or has at any time
been an Affiliate of AGIX.
(ii) The Royalties required to be paid with respect to any
particular country and any particular Calendar Quarter pursuant to Section 8.3
shall be subject to a reduction by AstraZeneca in an amount equal to [****] of
the amount of Third Party Royalties (other than royalties and other payments
paid pursuant to the Pre-Existing Third Party Licenses arising out of the
Development or Commercialization of Products) that are paid by AstraZeneca in
such country during such Calendar Quarter; provided however, that:
(A) such reduction may be made only to the extent such
Third Party Royalties have not previously been subject to reduction
pursuant to this Section 8.4; and
(B) no reductions in royalties otherwise due to AGIX
shall exceed an amount equal to [****]of the amount otherwise due in such
country pursuant to Section 8.3 for such Calendar Quarter.
Any amount that has not been reduced on such date because of this Section 8.4
shall not be eligible for further reduction in any succeeding royalty payment or
payments due for
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[****] indicates that certain confidential information contained in this
document has been omitted pursuant to a request for confidential treatment and
filed separately with the Securities and Exchange Commission.
45
such Product. AstraZeneca shall be responsible for any financial obligations
accruing after the Effective Date under the Pre-Existing Third Party Licenses
arising out of the Development or Commercialization of Products. AGIX shall not
amend a Pre-Existing Third Party License without the prior written consent of
AstraZeneca; provided, however, that consent shall not be unreasonably withheld;
provided further that AstraZeneca shall be permitted to withhold consent for any
amendment that materially increases costs or that decreases AstraZeneca's rights
under such Pre-Existing Third Party License.
(c) Generic Competition. Notwithstanding anything else to the
contrary in this Agreement, for any Product in any country in the Territory, if
and so long as there is Generic Competition with respect to such Product, then
AstraZeneca shall not be obligated to pay AGIX any Royalties pursuant to this
Agreement in respect of Net Sales for such Product in such country. If Generic
Competition commences and no longer exists in such country for such Product,
then the Royalty obligations for Net Sales of such Product in such country shall
be reinstated from the date of cessation of such Generic Competition until the
end of the Royalty Term, or until Generic Competition occurs again in such
country for such Product.
(d) Sublicenses
(i) During the applicable Royalty Term in each country in the
Territory, for any Compulsory Sublicense, AstraZeneca will pay AGIX, no later
than forty-five (45) days following the end of the preceding Calendar Quarter, a
payment equal to [****] of all amounts received by AstraZeneca as consideration
during such Calendar Quarter for any Compulsory Sublicense (either from the
Sublicensee or any other Third Party) in the form of milestones, royalty
payments or any other form of consideration (including, if the Sublicensee
purchases Product from AstraZeneca for resale, the gross sales price paid by
such Sublicensee minus AstraZeneca's costs for Manufacture of such Product),
subject to adjustment in accordance with Section 8.4.
(ii) Sales of Products under or as a result of Noncompulsory
Sublicenses, for purposes of the definition of "Net Sales" and for calculating
royalties under this Section 8.4, shall be deemed to be "Net Sales" by
AstraZeneca.
(e) Coated Stents. Notwithstanding anything else in this Section 8
to the contrary, if the JMC approves the Development and Commercialization of
Coated Stents, the Parties will, prior to Product Launch of any such Product,
negotiate in good faith the Royalties and any other payments to be paid to AGIX
in respect of sales of such Product, with such terms to be based on terms then
prevailing in comparable arrangements involving Third Parties and all other
relevant factors.
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[****] indicates that certain confidential information contained in this
document has been omitted pursuant to a request for confidential treatment and
filed separately with the Securities and Exchange Commission.
46
(f) Combination Products
(i) For Combination Products containing one or more Exclusive
Market Product(s), in each country in which such Combination Product is sold,
Net Sales shall be adjusted as follows:
(A) Net Sales shall be multiplied by the Net Sales of
the Combination Product during the applicable Calendar Quarter by the
fraction A/(A+B), where A is the Standard Sales Price of the Product
containing the same amount of Compound as the sole active ingredient as
the Combination Product in question in such country and B is the Standard
Sales Price of the ready for sale product containing the same amount of
the other therapeutically active ingredient that is contained in the
Combination Product in question in such country, in each case during the
applicable Calendar Quarter. For clarity, if a Combination Product
contains three or more active ingredients (including the Product), the
Standard Sale Price of such additional Exclusive Market Products ,
calculated in the same manner as described above, shall be included in the
denominator so that such fraction shall be A/(A+B1+ B2+...).
(B) If sales of the Product or the Exclusive Market
Product did not occur in such Calendar Quarter, then the most recent
previous Standard Sales Price of the Product containing the same amount of
Compound as the sole active ingredient as the Combination Product in
question in the given country, shall be used. If, in a specific country,
both a Product containing the Compound(s) and a product containing the
other active ingredients in such Combination Product are not sold
separately, a market price for such Product and such other active
ingredients shall be negotiated by the Parties in good faith based upon
the costs, overhead and profit as are then incurred for such Combination
Product and all Products then being made and marketed by AstraZeneca and
having an ascertainable market price that are comparable to such Product
or such other active ingredients, as applicable; provided, however, that
in no event shall the Royalty due to AGIX for such Combination Product be
less than [****] of what the Royalty would have been if the Net Sales for
such Combination Product were calculated by multiplying the number of
units of the Combination Product sold times the selling price of such
Product as if sold alone.
(C) Notwithstanding anything else in this Section
8.4(f)(i) to the contrary, if AstraZeneca or one of its Affiliates or
Sublicensees sells such a Combination Product in a country for less than
[****] of the sum of the then-Standard Sales Prices of the Product and the
Exclusive Market Product(s) that make up such Combination Product as sold
separately in finished form in such country, then in no event shall the
Royalty due to AGIX for such Combination Product be less than [****] of
what the Royalty would have been if
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[****] indicates that certain confidential information contained in this
document has been omitted pursuant to a request for confidential treatment and
filed separately with the Securities and Exchange Commission.
47
the Net Sales for such Combination Product were calculated by multiplying
the number of units of the Combination Product sold times the selling
price of the Product as if sold alone. If the Product is not then sold
separately in such country, then the most recent previous Standard Sales
Price in such country of such Product shall be used.
(ii) For Combination Products containing, as active
pharmaceutical ingredients, only Non-Exclusive Market Product(s) and a Product,
in each country in which such Combination Product is sold, the Net Sales for
such Combination Product shall be calculated by multiplying the number of units
of the Combination Product sold by the selling price of the Product as if sold
alone.
8.5 Payment; Report
(a) Reports. Following the First Commercial Sale of a Product,
AstraZeneca shall furnish to AGIX, within forty-five (45) days following the end
of each Calendar Quarter, a written report for such Calendar Quarter showing,
for each Product in each country in the Territory, (i) the adjustments resulting
from the deductions in the definition of "Net Sales" and from the calculation of
the amount of any applicable reductions or limitations pursuant to Section 8.4
to the extent reasonably available to AstraZeneca on a global basis; (ii) total
Net Sales; and (iii) the calculation of Royalties due.
(b) Records and Audit. AstraZeneca shall maintain, and shall require
its Affiliates and Sublicensees to maintain, for at least [****], complete and
accurate books and records in connection with the sale of Products as necessary
to allow the accurate calculation of the Royalties.
8.6 Exchange Rate; Manner and Place of Payment
(a) Payments. Unless otherwise specified in writing by the receiving
Party, all payments to be made by a Party making a payment under this Agreement
shall be made in United States dollars and shall be paid by bank wire transfer
in immediately available funds selected by the paying Party to a bank account
designated in writing by the receiving Party from time to time.
(b) Sales [****]. With respect to sales [****], Net Sales shall be
converted from the local currency to United States dollars based on applicable
currency exchange rates (as provided in Section 8.6(c)), and royalty amounts
owed shall be calculated based on such dollar amounts and paid to AGIX.
(c) Exchange Rate. The conversion of non-U.S. dollar sales into U.S.
dollar sales shall be calculated in accordance with AstraZeneca's then current
foreign exchange conversion methodology for external financial reporting to the
Securities and Exchange Commission.
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[****] indicates that certain confidential information contained in this
document has been omitted pursuant to a request for confidential treatment and
filed separately with the Securities and Exchange Commission.
48
(d) Tax Liability. In the event that, between the Effective Date and
the end of AGIX's second full tax year after Product Launch, any amount paid by
AstraZeneca to AGIX under this Section 8 suffers tax to be withheld by
AstraZeneca under applicable law or regulation ("Withholding Tax") for which
AGIX cannot obtain offset against U.S. corporate tax liability before foreign
tax credit for that year, then AstraZeneca shall, upon AGIX's claim to be
delivered in writing within four (4) months of the end of the relevant year,
advance AGIX the amount of such Withholding Tax to the extent that such offset
has not been obtained. Within thirty (30) days after the actual filing date of a
subsequent U.S. federal income tax return on which any amount of such
Withholding Tax so advanced under the preceding paragraph is offset against
AGIX's U.S. corporate tax liability as filed, AGIX shall repay to AstraZeneca
the corresponding amount previously advanced to AGIX by AstraZeneca, without
interest. In any event, all amounts advanced under this Section 8.6(d) by
AstraZeneca to AGIX shall, to the extent not previously repaid pursuant to the
immediately preceding sentence, be repaid by AGIX to AstraZeneca, without
interest, no later than the [****] of the Product Launch. For the avoidance of
doubt, [****]. AGIX will provide to AstraZeneca (or an agreed independent Third
Party accountant at AGIX's cost) upon the occasion of each advance and within
(30) days of filing of each relevant U.S. federal income tax return, supporting
documentation or a statement from their auditors or appointed tax advisers that
is sufficient to evidence the extent to which the Withholding Tax paid and
temporarily borne by AstraZeneca can or cannot be credited wholly or in part
against AGIX's U.S. tax for the relevant year when so prioritized.
(e) Income Tax Withholding. Subject to Section 8.6(d), each Party
shall pay any and all taxes levied on account of any license fee, royalty or
milestone payments made to it under this Agreement. If any taxes are required by
applicable law or regulation to be withheld by a Party, such Party shall (i)
deduct such taxes from the payment made to the other Party, (ii) timely pay the
taxes to the proper Governmental Authority, and (iii) send proof of payment to
the other Party and certify its receipt by the Governmental Authority within
thirty (30) days following such payment. If AGIX is entitled, subject only to
any requirement to file a prescribed form or other documentation, the
preparation and filing of which would not be unduly burdensome, under any
applicable tax treaty or local law to a reduction of rate of any applicable
withholding tax, upon AstraZeneca's prompt request therefore, AGIX shall deliver
to AstraZeneca or the appropriate Governmental Authority (with the assistance of
AstraZeneca) such forms or documentation, and AstraZeneca shall apply the
reduced rate of withholding once formal confirmation of AGIX's entitlement
thereto has been received from the relevant tax authority
(f) Indirect Taxes. Notwithstanding anything else contained in this
Section 8.6, this Section 8.6(f) shall apply with respect to Indirect Taxes. All
payments are exclusive of Indirect Taxes. If any Indirect Taxes are chargeable
in respect of any payments, the paying Party shall pay such Indirect Taxes at
the applicable rate in respect of any such payments following the receipt, where
applicable, of an Indirect Taxes
-------
[****] indicates that certain confidential information contained in this
document has been omitted pursuant to a request for confidential treatment and
filed separately with the Securities and Exchange Commission.
49
invoice in the appropriate form issued by the receiving Party in respect of
those payments, such Indirect Taxes to be payable on the due date of the
Payments to which such Indirect Taxes relate.
(g) Late Fee. All past due amounts owed by one Party to the other
Party under this Agreement shall bear simple interest at the U.S. Prime Rate, as
reported by the Wall Street Journal, Eastern Edition, on the due date (or the
next Business Day if the due date is not a Business Day), calculated based on
the number of days between the actual date the payment is made and the date the
payment was due; provided, however, that in no event shall such rate exceed the
maximum legal annual interest rate. The payment of such interest shall not limit
a Party from exercising any other rights it may have as a consequence of the
lateness of any payment.
(h) Audits
(i) The Parties shall permit upon written notice to the other
Party, at its own expense, a certified public accountant or a person possessing
similar professional status and associated with an independent accounting firm
acceptable to the Parties to inspect, during normal business hours, and not more
than once in any Calendar Year, to audit the other Party's books and records as
may be reasonably necessary to verify the accuracy of the financial reports
furnished by the other Party pursuant to this Agreement or of any charges,
reimbursements or payments made by the other Party pursuant to this Agreement,
in respect of any Calendar Year ending not more than three (3) years prior to
the date of such notice.
(ii) Each Party recognizes that the Third Party performing any
audit for a Party may perform accounting services for a Party, and each Party
hereby waives any conflict of interest relating to the use of such accounting
firm.
(iii) Upon the expiration of the [****] following the end of
any Calendar Year (or [****] with respect to Section 8.6(d)), the calculation of
amounts payable with respect to such fiscal year shall be binding and conclusive
upon the Parties, and the Parties shall be released from any liability or
accountability with respect to payments for such year.
(iv) The report prepared by any Third Party, if used by a
Party, shall contain the conclusions of such Third Party regarding the audit and
shall specify that the amounts paid pursuant thereto were correct or, if
incorrect, the amount of any underpayment or overpayment.
(v) In the case of any payment of Royalties, if such report
shows any underpayment by AstraZeneca, AstraZeneca shall remit to AGIX within
thirty (30) days after receipt of such report, (A) the amount of such
underpayment; and (B) if such underpayment exceeds [****] of the total amount
owed for the Calendar Year then being audited, the reasonable and necessary fees
and expenses of such Third Party to
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[****] indicates that certain confidential information contained in this
document has been omitted pursuant to a request for confidential treatment and
filed separately with the Securities and Exchange Commission.
50
perform the audit, subject to reasonable substantiation thereof. If such report
shows any overpayment by AstraZeneca, then at AstraZeneca's option, such
overpayment shall either be refunded to AstraZeneca by AGIX within thirty (30)
days of receipt of the audit report, or be creditable against amounts payable by
AstraZeneca in subsequent payment periods.
(vi) The Parties agree that all information subject to review
under this Section 8.6(h) is Confidential Information and that each Party shall
retain and cause any Third Party used for any audit to retain all such
information in confidence.
8.7 Representations and Covenants Concerning Certain Matters
(a) Insurance. AstraZeneca is and, throughout the Term, will remain
a party to the insurance program designated internally as the AstraZeneca Group
Insurance Programme on the same basis as any other Affiliate in the internally
designated AstraZeneca Group. The AstraZeneca Group Insurance Programme policy
indemnifies each Affiliate of AstraZeneca Group, including AstraZeneca, for any
legal or contractual liability to compensate third parties for, inter alia,
product liability subject to the policy's terms, conditions and limitations.
(b) Balance Sheet. The unaudited balance sheet for AstraZeneca dated
December 15, 2005 that has been delivered to AGIX is true and correct in all
material respects and presents fairly the financial position of AstraZeneca as
of the date thereof.
(c) Material Restructuring. Each Party agrees that, in the event
that a Material Restructuring of such Party is contemplated, no later than
thirty (30) days prior to the consummation of such Material Restructuring, such
Party will advise the other Party of such contemplated Material Restructuring
and the Parties will discuss in good faith whether any amendments are required
to this Agreement to ensure continued performance under the agreement by both
Parties following any such Material Restructuring.
9. INTELLECTUAL PROPERTY
9.1 Ownership of Inventions; Obligation to Update
(a) Ownership of Inventions. Each Party shall own any inventions
that are first identified, discovered, developed, conceived or made solely by
its employees, agents or independent contractors in conducting their activities
hereunder.
(b) Assignment. Each Party shall promptly execute all papers and
instruments, and/or require, to the extent possible, its employees, agents,
consultants or
51
independent contractors to execute such papers and instruments, as applicable,
so as to effectuate the ownership of AGIX IP, AstraZeneca IP and Joint IP.
(c) Obligation to Supplement AGIX Compound Patents. AGIX shall amend
or supplement Exhibit 1A from time to time to include any Patent Controlled by
AGIX or its Affiliates after the Effective Date that claims or is directed
solely to the Compound or the Product or solely to the Development, Manufacture,
formulation or use of the Compound or the Product in the Field. Upon such
inclusion, any such Patent shall be deemed an "AGIX Compound Patent."
(d) Obligation to Supplement Other AGIX Patents. AGIX shall amend or
supplement Exhibit 1C from time to time to include any Patent Controlled by AGIX
or its Affiliates after the Effective Date that is necessary or useful for the
Development, Manufacture, Commercialization, use, sale, offer for sale or
importation of the Compound or any Products in the Field. Upon such inclusion,
any such Patent shall be deemed an "Other AGIX Patent."
(e) Joint Inventions; Joint Patents. Inventions that are identified,
discovered, developed, conceived or made jointly by employees, agents,
consultants or independent contractors of each Party shall be deemed "JOINT
INVENTIONS". To the extent that the Parties file Patents directed to Joint
Inventions, such Patents shall be deemed "JOINT PATENTS," and ownership thereof
shall be determined in accordance with United States patent laws. For purposes
of this Section 9, any Joint Patents filed by the Parties shall be treated as
AGIX IP.
9.2 IPC
(a) IPC. The Parties shall form the IPC, pursuant to Section 6.3(h),
which shall function under the procedures established in this Section 9.2, until
the Parties agree to disband such committee, to oversee, facilitate, discuss,
manage and implement the filing, procurement, enforcement, and defense of
intellectual property matters relating to this Agreement in accordance with the
terms hereof.
(b) Composition
(i) The IPC shall have two (2) named representatives of AGIX
and two (2) named representatives of AstraZeneca, who may or may not be members
of the JMC or the JDC. Each Party shall appoint its respective representatives
to the IPC and may, from time to time, substitute one or more of its
representatives, in its sole discretion, effective upon notice to the other
Party of such change.
(ii) The IPC shall be co-chaired by one (1) representative of
AGIX and one (1) representative of AstraZeneca.
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(iii) The IPC representatives shall have appropriate technical
or legal credentials, experience and knowledge, and ongoing familiarity with
Compounds, Products and related Patents and other intellectual property issues
arising under this Agreement. Members of the IPC may delegate from time to time
certain matters arising within the IPC as they from time to time deem
appropriate.
(iv) Each Party may designate its own internal or external
patent counsel (who may or may not be a member of the IPC) who may attend IPC
meetings ("IPC PATENT COUNSEL"). The Parties shall take reasonable efforts to
preserve the lawyer-client privilege and work product privilege applicable to
the communications and work of IPC Patent Counsel and other legal counsel, and
shall enter into a shared-interest agreement.
(v) Additional representatives or consultants may from time to
time, by mutual consent of the Parties, be invited to attend IPC meetings,
subject to such representative's or consultant's written agreement to comply
with the confidentiality and non-use obligations equivalent to those set forth
in Section 10, and provided that such additional representatives shall have no
vote.
(vi) Alliance Managers may attend any IPC meeting without
notice or consent.
(c) Governance. In matters where the IPC has jurisdiction to make
decisions, such decisions shall be made by unanimous vote, with each Party's
representatives on the IPC collectively having one (1) vote.
(i) In the event that the IPC cannot or does not, after good
faith efforts, reach agreement on an issue (including, but not limited to, the
inventorship and ownership of Patents and Joint Patents under Section 9.1(e))
within thirty (30) days (or such shorter period as may be appropriate if prompt
action is required), then such issue shall be referred to the officer employed
by each Party who is in charge of intellectual property matters. If such
officers cannot resolve such issue, such issue shall then be referred to a
mutually agreed upon neutral outside patent counsel that has appropriate legal
and technical credentials; provided, however, that a Party may object to the
retention or continued retention of such counsel if such Party reasonably
believes such retention would be prejudicial to its intellectual property
interests (including, without limitation, conflicts of interest, such as if
outside counsel prosecutes patents for compounds similar to the Compound on
behalf of Third Parties, but excluding any perceived conflict of interest as a
result of the application of the standards described in Section 9.2(c)(ii)). A
list of appropriate counsel from which such neutral outside patent counsel may
be selected shall be created by the IPC promptly after the Effective Date and
approved by each Party. Such list may be updated from time to time as the IPC
deems appropriate. Such neutral outside counsel shall consider the interests of
both Parties when recommending a course of action. The IPC shall resolve issues
in a manner consistent with the recommendation of the neutral outside patent
counsel.
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(ii) For any decisions concerning a Patent made by the IPC, or
by the neutral counsel, described in Section 9.2.(c)(i),
(A) that involves a Compound-Only Issue, such decision
shall favor an outcome that allows for the strongest patentable scope of
patent rights afforded for the Compound, taking into account the invention
disclosed in light of any relevant prior art, and the longest possible
term for such Patent.
(B) that involves a Mixed Issue, such decision shall
favor an outcome that allows for the strongest patentable scope of patent
rights afforded for the Compound, taking into account the invention
disclosed in light of any relevant prior art, and the longest possible
term for such Patent; provided, however that such decision may not
reasonably, materially jeopardize the validity, enforceability or scope of
any claim of any Licensed Patent.
(iii) The IPC may establish and revise from time to time rules
for operation, in such form and detail as the IPC considers appropriate.
(d) Authority and Jurisdiction
(i) The IPC's decision-making authority shall be limited to
matters related to Licensed Patents, Blocking Patents, Orange Book listings and
patent term extensions. The IPC will discuss (but not decide) the status of
AstraZeneca Patents, AGIX Know-How and AstraZeneca Know-How, and will discuss
and review data and information, consider and advise on any technical issues
that arise, and discuss patent application filing priorities.
(ii) In no event shall the IPC have the right:
(A) to modify or amend the terms and conditions of this
Agreement;
(B) to review, direct or control, or make any decisions
or determinations with respect to, the Development or Commercialization or
Manufacturing of the Compound or Product (except with respect to Patent or
other intellectual property issues relating thereto);
(C) to determine which personnel of a Party perform
activities relating to matters affecting AGIX IP, or act as such Party's
representatives on the IPC;
(D) to make any decision with respect to a Party's
Prosecution activities, except as provided for in Section 9.3; and
54
(E) to determine any such issue in a manner that would
conflict with the express terms and conditions of this Agreement.
(e) Meetings
(i) The IPC shall meet in accordance with a schedule
established by mutual written agreement of the Parties, but no less frequently
than twice per year, with the location for such meetings to be mutually agreed
by the Parties, with the first meeting of the IPC to occur no later than fifteen
(15) days after the Effective Date.
(ii) Either Party may call for non-scheduled meetings of the
IPC upon reasonable notice, which shall occur at mutually agreeable times. The
IPC, upon mutual agreement, may meet in person or by means of teleconference,
videoconference, Webex or other similar communications equipment.
(iii) No IPC meeting may be conducted unless at least one (1)
representative of each Party is participating.
(iv) Each Party shall bear its own expenses related to the
attendance of such meetings by its representatives.
9.3 Patent Prosecution
(a) Prosecution. As used herein, "PROSECUTION" shall mean the
preparation, filing, prosecution and maintenance of patents or patent
applications and includes any procedure or practice before an administrative
agency such as the United States Patent and Trademark Office, or an equivalent
agency, including but not limited to interferences, reexaminations,
examinations, protests, reissues, oppositions, and the like.
(b) Prosecution Activities
(i) Subject to Section 9.3(b)(ii), AGIX shall control
Prosecution of all Licensed Patents and Joint Patents, under the direction of
the IPC. AstraZeneca shall have the right to comment on Prosecution activities
by AGIX to the extent that such activities involve a Licensed Patent or Joint
Patent. AGIX shall identify any such Prosecution activity to the IPC and provide
the IPC copies of any official action, filing (including a draft patent
application), communication, proposed submission in response to, and associated
data or information, in a timely manner but in no case less than fourteen (14)
days prior to the date any response to such official action or said application
is proposed to be filed. AGIX and its patent counsel will reasonably consider
AstraZeneca's comments thereon. If AstraZeneca does not provide AGIX with timely
comments, AGIX shall be free to proceed with its submission or other
contemplated action consistent with the direction of the IPC.
55
(ii) For any pending patent applications within the Licensed
Patents or any new patent applications that would otherwise be included in the
Licensed Patents that the IPC believes should be filed, AGIX shall file and
Prosecute patent applications or, if in the IPC's judgment the filing or
prosecution of such applications would materially adversely affect any Licensed
Patents, claims within patent applications, that in either case claim or are
directed solely to the Compound or Product, or the Development, Manufacturing,
formulation or use thereof. Any Prosecution activity in such patent application
shall be directed by the IPC, in accordance with Section 9.3(b)(i), and
implemented by AGIX in a manner consistent with Section 9.2(c)(ii).
(c) AstraZeneca Prosecution Activities. AstraZeneca shall control
Prosecution of all AstraZeneca Patents, at its sole expense; provided, however,
that AstraZeneca shall reasonably consider AGIX's comments thereon. AstraZeneca
shall identify any such Prosecution activity to the IPC and provide the IPC
copies of any official action, filing (including a draft patent application),
communication, proposed submission in response to, and associated data or
information, in a timely manner but in no case less than fourteen (14) days
prior to the date any response to such official action or said application is
proposed to be filed. AstraZeneca and its patent counsel will reasonably
consider AGIX's comments thereon; provided, however, that resolution of any
issue under this Section 9.3(c) shall be decided by AstraZeneca in its
discretion.
(d) Cooperation. In connection with any Prosecution activity, AGIX
and AstraZeneca shall cooperate fully and will provide each other with any
information or assistance that either Party reasonably requests, including
executing all documents necessary with respect to any such Prosecution activity.
If either Party becomes aware of any patents, information or proceeding that
relate to a Licensed Patent or Joint Patent and that may adversely impact the
validity, title or enforceability of such Licensed Patent or Joint Patent in the
Territory, such Party shall promptly notify the other Party of such patent,
information or proceeding; provided however that neither Party shall be
obligated to disclose any information that would cause such Party to violate any
confidentiality or nondisclosure obligation to a Third Party.
(e) Abandonment. If AGIX elects to abandon or discontinue
prosecution of or not maintain any claim in a Licensed Patent or Joint Patent
anywhere in the Territory, then AGIX shall provide AstraZeneca with thirty (30)
days' prior written notice of such determination, and shall provide AstraZeneca
with the right, but not the obligation, to prosecute and maintain such claim at
AstraZeneca's sole expense and, if requested by AstraZeneca, AGIX will
reasonably assist AstraZeneca with the prosecution and maintenance of the
Licensed Patent or Joint Patent. If AGIX elects to abandon or discontinue
prosecution of a Joint Patent and AstraZeneca elects to prosecute such Joint
Patent, AGIX will assign its interests in such Joint Patent to AstraZeneca. If
AstraZeneca elects to abandon or discontinue prosecution of or not maintain any
claim in an AstraZeneca Patent or Joint Patent anywhere in the Territory, where
such claim is
56
necessary or useful for the Development, Manufacture, Commercialization, use,
sale, offer for sale or importation of the Compound or any Product in the Field,
then AstraZeneca shall provide AGIX with thirty (30) days' prior written notice
of such determination, and shall provide AGIX with the right, but not the
obligation to prosecute and maintain such claim at AGIX's sole expense and, if
requested by AGIX, AstraZeneca will reasonably assist AGIX with the prosecution
and maintenance of the AstraZeneca Patent.
(f) Interference, Opposition, Protest, Reexamination and Reissue
(i) AGIX shall inform the IPC of any request for, or filing or
declaration of, any interference, opposition, protest, reexamination or reissue
relating to any claim in a Licensed Patent or Joint Patent within thirty (30)
days of learning of such event. The IPC shall review and consult with AGIX
regarding any submission to be made in connection with such proceeding. AGIX
shall give the IPC timely notice of any proposed settlement of an interference
relating to any Licensed Patents or Joint Patents.
(ii) AGIX shall conduct all activities in respect of any such
proceedings in accordance with the direction of the IPC. Any decisions made by
the IPC shall be made in accordance with Section 9.2(c)(ii).
(g) Patent Term Extension. Where directed by the IPC, AGIX shall use
reasonable efforts to obtain patent term extension or supplemental protection
certificates or their equivalents in any country in the Territory where
applicable to any Licensed Patent or Joint Patent that claims or is directed to
a Compound or Product, and AstraZeneca shall provide reasonable assistance to
AGIX (including the provision of copies of any necessary documents) to apply for
such extension.
(h) Expenses. Reasonable costs incurred by AGIX for any Prosecution
activities described in this Section 9.3 shall be reimbursed in accordance with
the procedures described in Section 9.9.
9.4 Patent Marking. Each Party shall xxxx all Products made, used or sold
under the terms of this Agreement, or their containers, in accordance with all
applicable patent-marking laws.
9.5 Infringement by Third Parties
(a) Notice. If either Party learns of any infringement of any
Licensed Patent or Joint Patent, or any misappropriation or misuse of AGIX
Know-How, such Party shall promptly notify the IPC in writing of such
infringement, misappropriation or misuse; provided, however that neither Party
shall be obligated to disclose any information that would cause such Party to
violate any confidentiality or nondisclosure obligation to a Third Party.
57
(b) Right to Bring and Prosecute Suit
(i) AGIX shall have the first right, but not the obligation,
to initiate and prosecute any legal action or other action or defense with
respect to any infringement of the Licensed Patents or Joint Patents or
misappropriation or misuse of AGIX Know-How by Third Parties, or to assume the
defense in any declaratory judgment action relating thereto, and if necessary,
to name AstraZeneca as a co-party. AstraZeneca shall cooperate fully with AGIX
in any such action. AstraZeneca shall have the right in any action or defense
brought under this Section 9.5(b)(i) to join such action voluntarily, at its own
expense, in which case the Parties shall cooperate fully in all reasonable
respects and will provide each other with any information or assistance that
either Party reasonably requests in connection with any such action.
(ii) If such action involves an AGIX Compound Patent and if,
within ninety (90) days of receiving the notice provided for in Section 9.5(a)
or thirty (30) days before the time limit, if any, set forth in the appropriate
laws and regulations for the filing of such actions, whichever comes first, AGIX
fails to institute or prosecute such action, or if AGIX informs AstraZeneca that
it elects not to exercise such first right, AstraZeneca thereafter shall have
the right to initiate and prosecute such action, or to assume the defense of
such declaratory judgment action, and if necessary, to name or retain AGIX as a
co-party. AGIX shall cooperate fully with AstraZeneca in any such action.
(iii) Except as provided in Section 9.5(b), any legal action,
other action or defense prosecuted or assumed by either AGIX or AstraZeneca
under this Section 9.5(b), including the decision to initiate any such action,
shall be subject to the direction and control of the IPC.
(iv) Any decision by AGIX not to initiate any action under
Section 9.5 that involves an Other AGIX Patent but that does not involve any
claims in the Field shall be made by AGIX in its sole discretion and shall not
be subject to the direction or control of the IPC.
(c) Certifications. Each Party shall inform the other Party of any
certification regarding any Licensed Patent that it has received pursuant to
either 21 U.S.C. Sections 355(b)(2)(A)(iv) or (j)(2)(A)(vii)(IV) or its
successor provisions, or Canada's Patented Medicines (Notice of Compliance)
Regulations Article 5, or any similar provisions in a country other than the
United States and Canada, and shall provide the other Party with a copy of such
certification within five (5) days of receipt by such Party. AGIX's and
AstraZeneca's rights with respect to the initiation and prosecution of any legal
action as a result of such certification or any recovery obtained as a result of
such legal action shall be as defined in this Section 9.5.
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9.6 Infringement of Third Party Rights
(a) Notice. If any Product Manufactured, used or sold by either
Party, its Affiliates, licensees or Sublicensees under this Agreement becomes
the subject of a Third Party claim, or there is a reasonable and credible basis
for a potential claim, of patent infringement relating to the Manufacture, use,
sale, offer for sale or importation of a Compound or Product, the Party first
having notice of the claim shall promptly notify the other Party, and the
Parties shall promptly thereafter meet to consider the claim and the appropriate
course of action.
(b) Defense
(i) The Party against which the action is brought shall have
the right, but not the obligation, to defend itself against such claim or
initiate any declaratory judgment action relating to a Compound or Product, or
bring any such action necessary to protect its interest in such Compound or
Product.
(ii) The Party not defending against such claim or initiating
a declaratory judgment action shall have a full right to participate in any such
action at its own expense.
(iii) The Party that defends any claim, or that brings any
declaratory action, under this Section 9.6(b), shall keep the IPC informed of
all material developments in any proceeding involving such defense or action.
The IPC may discuss any matters affecting such defense or action, but shall not
have the authority to direct any matter in such defense or action.
9.7 Cooperation
(a) Joining Action and Documentation. Notwithstanding anything to
the contrary in Section 9.5 or 9.6, for any action to terminate or defend
against claims of any infringement described in Section 9.5 or 9.6, if either
Party is unable to initiate or prosecute such action or defense solely in its
own name, the other Party shall join such action voluntarily and shall execute
all documents necessary to initiate litigation to prosecute and maintain such
action or defense. In connection with any such action, AGIX and AstraZeneca
shall cooperate fully in all reasonable respects and will provide each other
with any information or assistance that either reasonably requests, including if
required, furnishing a power of attorney, giving testimony, producing documents
lawfully requested and using reasonable and diligent efforts to make available
such employees who may be helpful with respect to such litigation action or
defense. Any costs incurred as the result of such cooperation shall be borne
equally by the Parties and subject to reimbursement in accordance with the
procedures described in Section 9.9.
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(b) Information and Decision-making by IPC. Each Party shall keep
the other Party informed of developments in any action or proceeding described
in Sections 9.5 and 9.6, including, to the extent permissible by law, the
consultation and approval of any offer related thereto. All information and
developments in any such action or proceeding shall be reported to the IPC and
each Party shall reasonably consider or follow the direction and advice and
consultation of the IPC with respect to any such action as provided in this
Section 9.
9.8 Awards and Recovery
(a) Reasonable out-of-pocket costs and expenses incurred by a Party
in respect of any action described in Section 9.5 or 9.6, including without
limitation attorney's fees, filing and court fees, and travel expenses, shall be
borne equally by the Parties. Reimbursement for any such costs shall be in
accordance with the procedures described in Section 9.9.
(b) Any recovery obtained by either Party in connection with or as a
result of any action contemplated by Section 9.5 or 9.6, whether by settlement
or otherwise, shall be shared in order as follows:
(i) Such recovery shall first be allocated to the Parties for
reimbursement in respect of their proportional costs and expenses incurred in
connection with the action after giving effect to the reimbursement provided for
in Section 9.9; and
(ii) Any remaining amounts after such reimbursement of the
Parties' costs and expenses shall be [****]to AGIX and [****] to AstraZeneca,
unless AGIX and AstraZeneca otherwise agree in writing.
9.9 Costs
(a) Within thirty (30) days following the end of each Calendar
Quarter, each Party will send a statement of reasonable out-of-pocket costs
incurred under Section 9.3, or by either Party under Section 9.2, 9.5 or 9.6 (in
such form and manner as the Parties shall agree from time to time) to the IPC
for consideration and review; provided, however, that any costs incurred related
to Pre-Existing Third Party Licenses arising out of the Development or
Commercialization of Products shall be borne by AstraZeneca.
(b) The IPC shall, within fifteen (15) days after receipt of the
statements described in Section 9.9(a), determine whether the amounts reflected
therein are reasonable and, to the extent such amounts are so determined to be
reasonable, determine the net difference ("NET DIFFERENCE") between such
reasonable amounts reflected in such two statements.
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[****] indicates that certain confidential information contained in this
document has been omitted pursuant to a request for confidential treatment and
filed separately with the Securities and Exchange Commission.
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(c) Following the determination pursuant to Section 9.9(b), the
Party that incurred the lower costs in such Calendar Quarter shall pay to the
other Party, within sixty (60) days of the end of such Calendar Quarter, an
amount equal to [****] of the Net Difference for such Calendar Quarter.
(d) Any issues discussed by the IPC pursuant to this Section 9.9,
which cannot be resolved by unanimous vote pursuant to Section 9.2(c) shall be
determined pursuant to Section 14.
9.10 Trademarks
(a) The Global Commercialization Team shall in good faith select
Product Trademarks. The Global Commercialization Team may change the Product
Trademarks at any time in its sole discretion upon the exercise of its good
faith judgment. AstraZeneca shall own all Product Trademarks and be responsible
for registering, maintaining and enforcing such Trademarks throughout the
Territory. AstraZeneca shall also own any domain names directly associated with
the Product in the Territory.
(b) In the Territory, the Parties agree to work together in a
cooperative fashion to cause, to the extent permitted by the FDA, the corporate
Trademarks of both Parties to (i) appear in equal prominence on any Product
package inserts, main promotional pieces for professionals (e.g., detail aids
and printed advertisements), smaller promotional pieces where practical,
exhibition stand panels and monographs; and (ii) be referenced at all
investigator meetings and symposia, all Product specific press releases, and any
direct to consumer advertising.
(c) AGIX hereby grants AstraZeneca a non-exclusive, royalty free
license to use AGIX's corporate Trademarks solely for purposes of
Commercializing Products, which license shall terminate upon the expiration or
earlier termination of this Agreement for any reason.
(d) No Ownership or Rights in the Product Trademarks
(i) Except as otherwise expressly set forth in this Section
9.10, nothing in this Agreement shall give either Party any rights, title or
interest in and to any other Trademarks that are owned, licensed or maintained,
as the case may be, by the other Party. AGIX acknowledges and agrees that
AstraZeneca or its Affiliates, as the case may be, are the owners of all rights,
title and interest in and to the Product Trademarks, including any form or
embodiment thereof, and the goodwill now and hereafter associated with the
Product Trademarks. AstraZeneca and its Affiliates acknowledge and agree that
AGIX is the owner of all rights, title and interest in and to AGIX's corporate
Trademarks, including any form or embodiment thereof, and the goodwill now and
hereafter associated with the AGIX corporate Trademarks.
-------
[****] indicates that certain confidential information contained in this
document has been omitted pursuant to a request for confidential treatment and
filed separately with the Securities and Exchange Commission.
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(ii) Neither Party shall, or knowingly cause another person
to, contest or dispute or otherwise impair or endanger the validity of, or the
exclusive rights of any Trademark, including Product Trademarks, owned, licensed
or maintained, as the case may be, of the other Party or its Affiliates, or any
part thereof, or the registrations thereof.
(iii) AGIX acknowledges that all use of the Product Trademarks
by or on behalf of AGIX shall inure to the benefit of AstraZeneca or their
respective Affiliates, as the case may be. AGIX shall not be entitled to any
compensation for any increase in the value of the Product Trademarks or in the
goodwill associated therewith. AGIX (upon written request of AstraZeneca) shall
assist AstraZeneca and their respective Affiliates to safeguard their full
rights, title and interest in and to the Product Trademarks.
10. CONFIDENTIALITY
10.1 Nondisclosure Obligation
(a) Confidential Information. All information disclosed by one Party
to the other Party hereunder, including the terms of this Agreement
("CONFIDENTIAL INFORMATION"), shall be maintained in confidence by the receiving
Party and shall not be disclosed to any non-Party or used for any purpose except
to exercise its rights and perform its obligations under this Agreement without
the prior written consent of the disclosing Party, except to the extent that the
receiving Party can demonstrate by competent written evidence that such
Confidential Information:
(i) is known by the receiving Party at the time of its receipt
and, not through a prior disclosure by the disclosing Party, as documented by
the receiving Party's business records;
(ii) is in the public domain other than as a result of any
breach of this Agreement by the receiving Party;
(iii) is subsequently disclosed to the receiving Party on a
non-confidential basis by a Third Party who may lawfully do so; or
(iv) is independently discovered or developed by the receiving
Party without the use of Confidential Information provided by the disclosing
Party, as documented by the receiving Party's business records.
(b) Return of Confidential Information Upon Expiration or
Termination of Agreement. Within thirty (30) days after any expiration or
termination of this Agreement, each Party shall destroy (and certify to the
other Party such destruction) or return such Confidential Information provided
by the other Party as the other Party reasonably requests be destroyed or
returned; provided, however, that (i) the foregoing
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obligation shall not apply to any matter of Confidential Information otherwise
provided for in this Agreement; and (ii) each Party may retain a single copy of
the Confidential Information in its confidential legal files for the sole
purpose of ascertaining its ongoing rights and responsibilities regarding the
Confidential Information.
10.2 Permitted Disclosures
(a) Permitted Disclosure. Each Party may disclose Confidential
Information provided by the other Party without such other Party's written
consent to the extent such disclosure is reasonably necessary in the following
instances:
(i) disclosure to governmental or other regulatory agencies in
order to obtain or maintain Patents on Licensed Patents and Joint Patents and to
obtain, maintain or amend any Regulatory Materials regarding a Product or
satisfy any other regulatory obligation regarding a Product, but such disclosure
may be only to the extent reasonably necessary to obtain Patents or obtain,
maintain or amend such Regulatory Materials;
(ii) complying with applicable court orders or governmental
regulations, including without limitation rules or regulations of the Securities
and Exchange Commission, or by rules of the National Association of Securities
Dealers, any securities exchange or NASDAQ; provided, however, that the
receiving Party shall first have given notice to the other Party hereto in order
to allow such Party the opportunity to seek confidential treatment of the
Confidential Information;
(iii) disclosure to consultants, agents or other Third Parties
solely to the extent required to accomplish the purposes of this Agreement or in
connection with due diligence or similar investigations by such Third Parties;
provided however that such Third Parties agree to be bound by confidentiality
and non-use obligations at least equivalent in scope to those contained in this
Agreement.
(b) Written Agreements. Each Party shall obtain written agreements
from each of its employees and consultants who perform work pursuant to this
Agreement, which agreements shall obligate such persons to similar obligations
of confidentiality and to assign to such Party all inventions made by such
persons during the course of performing such work. Each Party will notify the
other Party promptly upon discovery of any unauthorized use or disclosure of the
Confidential Information of the other Party.
(c) Required Disclosure. If a Party is required by judicial or
administrative process to disclose Confidential Information that is subject to
the non-disclosure provisions of Section 10.1, such Party shall promptly inform
the other Party of the disclosure that is being sought in order to provide the
other Party an opportunity to challenge or limit the disclosure obligations,
provided that such Party's obligations to
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comply with Applicable Laws shall not be affected by such obligations.
Confidential Information that is disclosed by judicial or administrative process
shall remain otherwise subject to the confidentiality and non-use provisions of
this Section 10.2(c), and the Party disclosing Confidential Information pursuant
to law or court order shall take all reasonable steps necessary, including
without limitation obtaining an order of confidentiality, to ensure the
continued confidential treatment of such Confidential Information.
10.3 Use of Name. Neither Party shall use the name of the other Party,
without the prior written approval of the other Party, for any purpose other
than informing employees who need to know about this Agreement; provided,
however, that AstraZeneca may, without AGIX's prior written approval, use AGIX's
name on marketing materials that were developed by or under the direction of the
US Commercialization Team or Global Commercialization Team. Without limitation,
these prohibitions apply to press releases, annual reports, prospectuses, public
statements, educational and scientific conferences, Promotional Materials,
governmental filings and discussions with public officials, securities analysts,
investors and the media. However, subject to the requirements for review and
approval that follow, these prohibitions shall not apply to a disclosure of the
other Party's name, which counsel to a Party has advised is required by law or
regulation or in response to requests for a copy of this Agreement or related
information by tax authorities.
10.4 Publicity. It is understood that the Parties intend to issue
coordinated press releases announcing the execution of this Agreement and agree
that each Party may desire or be required to issue subsequent press releases
relating to the Agreement or activities hereunder. The Parties agree to consult
with each other reasonably and in good faith with respect to the text and timing
of such press releases prior to the issuance thereof, provided that a Party may
not unreasonably withhold consent to such releases, and that either Party may
issue such press releases as it determines, based on advice of counsel, are
reasonably necessary to comply with laws or regulations or for appropriate
market disclosure. In addition, following the initial press releases announcing
this Agreement, each Party shall be free to disclose, without the other Party's
prior written consent, the existence of this Agreement, the identity of the
other Party and those terms of the Agreement which have already been publicly
disclosed in accordance herewith.
(a) Publicity Referral. Unless otherwise directed in writing by
AstraZeneca, all matters that require AstraZeneca's review or consent under this
Section must be referred to the Corporate Communications Department for review
and approval at the address set forth in Section 15.7. Unless otherwise directed
in writing by AGIX, all matters that require AGIX's review or consent under this
Section must be referred to the Corporate Communications Department, at the
address set forth in Section 15.7.
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10.5 Publications. The JMC shall develop procedures for review and
approval of publications related to a Product or other activities of the
Collaboration, and neither Party shall permit any publication in violation of
such procedures.
11. REPRESENTATIONS AND WARRANTIES
11.1 Corporate Existence and Authority. Each Party hereby represents and
warrants to the other Party that, as of the Execution Date, it:
(a) is a corporation duly organized, validly existing and in good
standing under the laws of the state, country or jurisdiction in which it is
incorporated;
(b) has full corporate power and authority and the legal right to
own and operate its property and assets and to carry on its business as it is
now being conducted and is contemplated in this Agreement and the Related
Agreements (without making any representation as to the intellectual property
rights except as otherwise specifically set forth in this Section 11); and
(c) has the corporate power and full authority and the legal right
to enter into this Agreement and perform the obligations and duties contemplated
under this Agreement and the Related Agreements.
11.2 Authorized Execution; Binding Obligation. Each Party represents and
warrants to the other Party that, as of the Execution Date (i) the execution,
delivery, and performance of the Agreement and the Related Agreements and the
consummation of the transactions contemplated thereby have been duly authorized
and approved by all necessary corporate action on its part; and (ii) this
Agreement and the Related Agreements have been duly executed and delivered by it
and constitute a legal, valid, and binding obligation enforceable against it in
accordance with such Agreement's terms, except as the same may be limited by
applicable bankruptcy, insolvency, reorganization, moratorium or other laws
relating to or affecting creditors' rights generally and by general equity
principles, including judicial principles affecting the availability of
injunction and specific performance.
11.3 No Conflicts. Each Party represents and warrants to the other Party
that its execution, delivery, and performance of this Agreement or the Related
Agreements:
(a) does not, except as otherwise described in this Agreement or, in
a Related Agreement, require the approval or consent of any Person, which has
not already been obtained except for those government approvals, if any, not
required at the time of execution of this Agreement;
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(b) does not, to the best of its knowledge, contravene any
Applicable Laws; and
(c) does not contravene the provisions of, nor constitute a default
under, its articles of incorporation or bylaws or any indenture, mortgage,
contract or other agreement or instrument to which it is a signatory, or any
permit, or governmental authorization or grant.
11.4 All Consents and Approvals Obtained. Except as otherwise described in
this Agreement, each Party represents and warrants to the other that (i) all
necessary consents, approvals and authorizations of, and (ii) all notices to,
and filings by such Party with, all governmental authorities and other persons
or entities required to be obtained or provided by such Party in connection with
the execution, delivery and performance of this Agreement and the Related
Agreements have been obtained and provided, except for those government
approvals, if any, not required at the time of execution of this Agreement.
11.5 AGIX Representations and Warranties. AGIX represents and warrants to
AstraZeneca as follows:
(a) Owned Patents and In-Licensed Patents. As of the Execution Date
and except as noted on Exhibit 11.5,
(i) AGIX is the sole and exclusive owner of the entire right,
title and interest in the Licensed Patents noted on Exhibit 11.5 as those owned
by AGIX (the "Owned Patents"), and is entitled to grant the licenses specified
herein.
(ii) The Owned Patents are not subject to any encumbrance,
lien or claim of ownership by any Third Party.
(iii) AGIX is the sole and exclusive licensee of, and Controls
all right, title and interest in and to the Licensed Patents noted on Exhibit
11.5 as licensed by AGIX (the "In-Licensed Patents") and is entitled to grant
the licenses specified herein. To the Knowledge of AGIX, such rights are not
subject to any encumbrance, lien or claim of ownership by any Third Party.
(b) Prosecution Documents. As of the Execution Date, true, complete
and correct copies of the complete file wrapper and other documents and
materials that relate to the prosecution, defense, maintenance, validity and
enforceability of the Owned Patents and the In-Licensed Patents and all licenses
and other agreements regarding the Licensed Patents, as amended, have been made,
or are available to AstraZeneca.
(c) Pre-Existing Third Party License. During the term of this
Agreement, AGIX shall not terminate any Pre-Existing Third Party License or
breach
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such license such that the other Party thereto would have the right to terminate
such license.
(d) Patent Prosecution. As of the Execution Date and except as set
forth on Exhibit 11.5, the Licensed Patents (i) have been, to the Knowledge of
AGIX, diligently prosecuted in accordance with all Applicable Laws and
regulations, and (ii) have been filed and maintained properly and correctly, and
all applicable fees have been paid to file and maintain such Licensed Patents.
(e) Non-Infringement by Third Parties. As of the Execution Date, to
the Knowledge of AGIX, there are no activities by Third Parties that would
constitute infringement or misappropriation of any Licensed Patents.
(f) Non-Infringement of Third Party Rights. As of the Execution
Date, to the Knowledge of AGIX, except as disclosed in Exhibit 11.5. there are
no Patents or trade secret rights owned or controlled by a Third Party, that
would be infringed or misappropriated by the Development, Manufacture or
Commercialization of Product(s), and AGIX has received no written claims
relating to any such infringement or misappropriation. As of the Execution Date,
to the Knowledge of AGIX, the use of Regulatory Materials did not infringe or
misappropriate any Patent or trade secret rights owned or controlled by a Third
Party.
(g) Validity and Misappropriation. As of the Execution Date and
except as set forth in Exhibit 11.5, to the Knowledge of AGIX, (i) the Licensed
Patents are subsisting, or pending, and are not invalid or unenforceable, in
whole or in part, and (ii) the conception, development and reduction to practice
of the Licensed Patents have not constituted or involved the misappropriation of
trade secrets or other rights or property of any Third Party.
(h) Regulatory Materials. AGIX has made available to AstraZeneca all
Regulatory Materials in its possession or Control regarding or related to the
Compound. As of the Execution Date, AGIX has prepared, maintained and retained
all Regulatory Materials required to be maintained or reported pursuant to and
in accordance with cGCP and cGLP, to the extent required, and Applicable Laws
and the Regulatory Materials do not contain any materially false and misleading
statements.
(i) Clinical Studies. AGIX has conducted, and has caused its
contractors and consultants to conduct, any and all clinical studies related to
the Compound in accordance with cGCP and cGLP, to the extent required, and
Applicable Laws.
(j) Existing Patents in the Territory. The Licensed Patents are not
subject anywhere in the Territory to any pending or, to the Knowledge of AGIX,
threatened re-examination, protest, opposition, interference or litigation
proceedings.
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(k) Employees and Agents. To the Knowledge of AGIX and except as set
forth on Exhibit 11.5, AGIX has obtained from its employees and Third Parties
involved, for or on behalf of AGIX, in the Development or Manufacture of the
Compound or Product(s) rights to information that relate to the Compound or
Product(s), that permit AGIX to grant to AstraZeneca the licenses and other
rights granted to AstraZeneca hereunder.
(l) Licensed Patents. As of the Execution Date, all of the Licensed
Patents listed on Exhibit 11.5 are all of the Patents Controlled by AGIX that
are necessary or useful for the Development, Manufacture, Commercialization,
use, sale, offer for sale or importation of the Compound in the Field.
11.6 Other Agreements
(a) AGIX represents to AstraZeneca that
(i) prior to the Execution Date, it has not entered into any
agreement, whether written or oral, or otherwise assigned, transferred,
licensed, conveyed or otherwise encumbered its right, title or interest in or
to, the AGIX IP, Regulatory Materials, or the Compound(including by granting any
covenant not to xxx with respect thereto), and
(ii) it will not enter into any such agreements or grant any
such right, title or interest to any Person,
that in the case of (i) or (ii) of this Section 11.6(a) has prevented or would
prevent AGIX from fulfilling its obligations under this Agreement.
(b) AstraZeneca represents to AGIX that
(i) it has not previously entered into any agreement, whether
written or oral, and
(ii) it will not enter into any such agreement or grant any
such right, title or interest to any Person,
that has prevented or would prevent AstraZeneca from fulfilling its obligations
under this Agreement.
11.7 Debarment. Each Party represents to the other Party that it has not
been debarred and is not subject to debarment and will not use in any capacity,
in connection with such Party's obligations under this Agreement, any Person who
has been debarred pursuant to Section 306 of the FD&C Act, or who is the subject
of a conviction described in such section. AGIX agrees to inform AstraZeneca in
writing immediately if it or any
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Person who is performing services hereunder is debarred or is the subject of a
conviction described in Section 306, or if any action, suit, claim,
investigation or legal or administrative proceeding is pending or, to the
Knowledge or AGIX, is threatened, relating to the debarment or conviction of
AGIX or any Person performing services hereunder.
11.8 Knowledge of Pending or Threatened Litigation. Each Party represents
and warrants to the other Party that, to its knowledge, there is no claim,
investigation, suit, action or proceeding pending or, expressly threatened,
against such Party before or by any governmental entity or arbitrator that is
likely to impair the ability of such Party to perform any obligation under this
Agreement.
11.9 Pre-Existing Third Party Licenses
(a) AGIX represents and warrants to AstraZeneca that
(i) the Pre-Existing Third Party Licenses are in full force
and effect and have not been modified or amended other than as shown therein;
(ii) neither AGIX nor, to the Knowledge of AGIX, any other
party to a Pre-Existing Third Party License is in default with respect to a
material obligation under, and neither such party has claimed or has grounds
upon which to claim that the other party is in default with respect to a
material obligation under a Pre-Existing Third Party License; and
(iii) AGIX has not waived or allowed to lapse any of its
rights under any Pre-Existing Third Party License, and no such rights have
lapsed or otherwise expired or been terminated.
(b) AGIX agrees that during the term of this Agreement:
(i) AGIX will use commercially reasonable efforts to fulfill
its obligations under each Pre-Existing Third Party License to the extent such
obligations have not been delegated to AstraZeneca and to the extent that
failure to do so would adversely affect AstraZeneca's or its rights hereunder;
(ii) AGIX shall not terminate any Pre-Existing Third Party
License in whole or in part, directly or indirectly, without AstraZeneca's prior
written consent;
(iii) AGIX shall promptly furnish AstraZeneca with copies of
all reports and other communications AGIX receives from any party to a
Pre-Existing Third Party License that relate to the subject matter of this
Agreement;
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(iv) AGIX shall promptly furnish AstraZeneca with copies of
all reports and other communications that AGIX furnishes to a party to a
Pre-Existing Third Party License that relate to the subject of this Agreement,
and to the extent any such reports or communications relate to the efforts of
AstraZeneca under this Agreement, AGIX shall give AstraZeneca a reasonable
opportunity to review and comment upon such reports or communications before
they are transmitted to any such other party;
(v) AGIX shall furnish AstraZeneca with copies of all notices
received by AGIX relating to any alleged breach or default by AGIX under any
Pre-Existing Third Party License within three (3) Business Days after AGIX's
receipt thereof and, if AGIX cannot or chooses not to cure or otherwise resolve
any such alleged breach or default, AGIX shall so notify AstraZeneca within five
(5) days thereafter and allow AstraZeneca, in AstraZeneca's sole discretion, to
cure or otherwise resolve any such alleged breach or default; and
(vi) AGIX, acting as an intermediary between each party to a
Pre-Existing Third Party License and AstraZeneca, shall allow AstraZeneca to
enjoy the direct benefit of all of AGIX's affirmative rights, to the extent they
relate to the Licensed Patents.
11.10 Disclaimer of Implied Warranties. EXCEPT AS EXPRESSLY PROVIDED IN
THIS AGREEMENT OR THE RELATED AGREEMENTS, NEITHER PARTY MAKES ANY OTHER
REPRESENTATION OR WARRANTY, EXPRESS OR IMPLIED, EITHER IN FACT OR BY OPERATION
OF LAW, STATUTE, OR OTHERWISE, AND EACH PARTY SPECIFICALLY DISCLAIMS ANY AND ALL
IMPLIED OR STATUTORY WARRANTIES INCLUDING WARRANTIES OF MERCHANTABILITY, OF
FITNESS FOR A PARTICULAR PURPOSE, AND OF NON-INFRINGEMENT.
11.11 Limitation of Liability. NEITHER PARTY SHALL BE LIABLE TO THE OTHER
PARTY FOR INDIRECT, INCIDENTAL, CONSEQUENTIAL, OR SPECIAL DAMAGES INCLUDING, BUT
NOT LIMITED TO, LOST PROFITS ARISING FROM OR RELATING TO ANY BREACH OF THIS
AGREEMENT, REGARDLESS OF ANY NOTICE OF THE POSSIBILITY OF SUCH DAMAGES. HOWEVER,
NOTHING IN THIS SECTION IS INTENDED TO LIMIT OR RESTRICT THE INDEMNIFICATION
RIGHTS OR OBLIGATIONS OF EITHER PARTY UNDER SECTION 12.
11.12 Guarantee of Performance of Affiliates. Each Party shall be liable
for the performance of such Party's Affiliates and absolutely, unconditionally
and irrevocably guarantees to the other Party: prompt performance when due and
at all times thereafter of the liabilities (including, without limitation,
indemnity obligations and liabilities), obligations, covenants, warranties,
representations and undertakings of its Affiliates pursuant to this Agreement
and the Related Agreements, and any and all modifications and amendments
thereof.
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12. INDEMNIFICATION
12.1 AstraZeneca Indemnification. AstraZeneca shall defend AGIX and its
Affiliates, and their respective agents, directors, officers and employees (the
"AGIX INDEMNITEES"), at AstraZeneca's cost and expense, and will indemnify and
hold harmless the AGIX Indemnitees from and against any and all losses, costs,
damages, fees or expenses (including reasonable attorneys' fees and other
litigation expenses) ("AGIX LOSSES") incurred by or awarded against an AGIX
Indemnitee relating to or in connection with any claim or action, regulatory
investigation, or any other cause, brought against any AGIX Indemnitee by a
Third Party arising out of:
(a) the labeling, packaging, marketing, use and sale of the
Products;
(b) to the extent not controlled by AGIX, the Development,
Manufacture and Promotion of the Products;
(c) any breach by AstraZeneca of its representations, warranties,
covenants or obligations made under this Agreement; or
(d) any negligent act or omission or willful misconduct of
AstraZeneca or its Affiliates or any of their employees, Sublicensees,
contractors or agents, in performing its obligations under this Agreement;
provided, however, that, the foregoing indemnity shall not apply to the extent
that any such AGIX Losses are (i) attributable to the gross negligence or
willful misconduct of the AGIX Indemnitees or (ii) otherwise subject to an
obligation by AGIX to indemnify AstraZeneca Indemnitees under Section 12.2 or
any Related Agreement.
12.2 AGIX Indemnification. AGIX agrees to defend AstraZeneca and its
Affiliates, and their respective agents, directors, officers and employees (the
"ASTRAZENECA INDEMNITEES"), at AGIX's cost and expense, and will indemnify and
hold harmless the AstraZeneca Indemnitees from and against any and all losses,
costs, damages, fees or expenses (including reasonable attorneys' fees and other
litigation expenses) ("ASTRAZENECA LOSSES") incurred by or awarded against an
AstraZeneca Indemnitee relating to or in connection with any claim or action,
regulatory investigation, or any other cause, brought against any AstraZeneca
Indemnitee by a Third Party arising out of:
(a) to the extent controlled by AGIX, the Development of the
Products;
(b) to the extent controlled by AGIX, the Promotion of the Products;
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(c) any breach by AGIX of its representations, warranties, covenants
or obligations made under this Agreement; or
(d) any negligent act or omission or willful misconduct of AGIX or
its Affiliates or any of their employees, Sublicensees, contractors or agents,
in performing its obligations under this Agreement; provided, however, that, the
foregoing indemnity shall not apply to the extent that any such AstraZeneca
Losses are (i) attributable to the gross negligence or willful misconduct of the
AstraZeneca Indemnitees, or (ii) otherwise subject to an obligation by
AstraZeneca to indemnify AGIX Indemnitees under Section 12.1 or any Related
Agreements.
12.3 Indemnification Procedures
(a) Notice. Promptly after an Indemnitee receives notice of a
pending or threatened claim, demand, suit, action or proceeding brought or
initiated by a Third Party (an "ACTION"), such Indemnitee shall give written
notice of the Action to the Indemnifying Party to whom the Indemnitee is
entitled to look for indemnification pursuant to this Section 12 (which notice
shall describe, among other things, the nature and amount being claimed in such
Action). However, an Indemnitee's delay in providing or failure to provide such
notice shall not relieve the Indemnifying Party of its indemnification
obligations, except to the extent it can demonstrate prejudice due to the delay
or lack of notice.
(b) Defense. Upon receipt of notice under Subsection (a) from the
Indemnitee, the Indemnifying Party shall have the duty to either compromise or
defend, at its own expense and by counsel (reasonably satisfactory to
Indemnitee) such Action. The Indemnifying Party shall promptly (and in any event
not more than twenty (20) days after receipt of the Indemnitee's original
notice) notify the Indemnitee in writing that it wishes to assume control of the
Action pursuant to this Section 12 and of its intention to either compromise or
defend such Action. The assumption of the defense of an Action by the
Indemnifying Party shall not be construed as an acknowledgement that the
Indemnifying Party is liable to indemnify the Indemnitee in respect of the
Action, nor shall it constitute a waiver by the Indemnifying Party of any
defenses it may assert against any Indemnified Party's claim for
indemnification. Once the Indemnifying Party gives such notice to the
Indemnitee, the Indemnifying Party is not liable to the Indemnitee for the fees
of other counsel or any other expenses subsequently incurred by the Indemnitee
in connection with such defense, other than the Indemnitee's reasonable costs of
investigation and cooperation. However, the Indemnitee shall have the right to
employ separate counsel and to control the defense of an Action (and the
Indemnifying Party shall bear the reasonable fees, costs, and expenses of such
counsel) if:
(i) the use of the counsel chosen by the Indemnifying Party
would present such counsel with a conflict of interest;
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(ii) the actual or potential defendants in, or targets of,
such Action include both the Indemnifying Party and the Indemnitee, and the
Indemnitee reasonably concludes that there may be legal defenses available to it
that are different from or additional to those available to the Indemnifying
Party (in which case the Indemnifying Party shall not have the right to assume
the defense of such Action on the Indemnitee's behalf);
(iii) the Indemnifying Party does not employ counsel
reasonably satisfactory to the Indemnitee to represent the Indemnitee within a
reasonable time after the Indemnitee's notice of such Action; or
(iv) in the reasonable opinion of counsel to the Indemnitee,
the claim could result in the Indemnitee becoming subject to injunctive relief
or relief other than the payment of Losses that could have a materially adverse
effect on the ongoing business of the Indemnitee; provided, however, that in no
event shall the Indemnifying Party be obligated to bear the fees, costs and
expenses of more than one (1) separate counsel for all of the other Party's
Indemnitees in such Action.
(c) Cooperation. The Indemnitee shall cooperate fully with the
Indemnifying Party and its legal representatives in the investigation and
defense of an Action. The Indemnifying Party shall keep the Indemnitee informed
on a reasonable and timely basis as to the status of such Action (to the extent
the Indemnitee is not participating in the defense of such Action) and conduct
the defense of such Action in a prudent manner.
(d) Settlement. If an Indemnifying Party assumes the defense of an
Action, no compromise or settlement of such Action may be effected by the
Indemnifying Party without the Indemnitee's written consent (which consent shall
not be unreasonably withheld or delayed), unless (i) there is no finding or
admission of any violation of law or any violation of the rights of any person
and no effect on any other claims that may be made against the Indemnitee, (ii)
the sole relief provided is monetary damages that are paid in full by the
Indemnifying Party, and (iii) the Indemnitee's rights under this Agreement are
not adversely affected. If the Indemnifying Party fails to assume defense of an
Action within a reasonable time, the Indemnitee may settle such Action on such
terms as it deems appropriate with the consent of the Indemnifying Party (which
consent shall not be unreasonably withheld), and Indemnifying Party shall be
obligated to indemnify the Indemnitee for such settlement as provided in this
Section 12.
12.4 Indemnification Payment Adjustments
(a) Insurance Proceeds Or Other Recovery. The amount of any Losses
for which indemnification is provided under this Section 12 shall be reduced by
the insurance proceeds received and any other amount recovered, if any, by the
Indemnitee with respect to any Losses. An Indemnitee shall mitigate, to the
extent such mitigation
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does not otherwise harm such Indemnitee or is otherwise inconsistent with this
Section 12, any Losses for which indemnification is sought hereunder and, to the
extent such Losses are covered by Indemnitee's insurance, shall pursue an
insurance claim relating to such Losses.
(b) Refund. If an Indemnitee receives a payment pursuant to this
Section 12 and subsequently receives insurance proceeds or other amounts with
respect to the same Losses, the Indemnitee shall pay to the Indemnifying Party
an amount equal to the difference (if any) between: (i) the sum of the insurance
proceeds received, other amounts received, and the indemnification amount
received from the Indemnifying Party pursuant to this Section 12 and (ii) the
amount necessary to fully and completely indemnify and hold harmless the
Indemnitee from and against such Losses. However, in no event shall such refund
ever exceed the Indemnifying Party's payment to the Indemnitee under this
Section 12.
12.5 Indemnification Payment. Any amount owed by an Indemnitee to a Third
Person, for which the Indemnifying Party has an obligation under this Section 12
to indemnify, shall be due from the Indemnifying Party to the Third Person,
whether upon entry of judgment, upon settlement, or otherwise.
12.6 Survival. The provisions of this Section 12 shall survive any
termination or expiration of this Agreement. Each Indemnitee's rights under this
Section 12 shall not be deemed to have been waived or otherwise affected by such
Indemnitee's waiver of the breach of any obligation, agreement, condition,
covenant, representation, or warranty contained in, or made pursuant to, this
Agreement, unless such waiver expressly (and in writing) also waives any or all
of the Indemnitee's rights under this Section 12.
13. TERM AND TERMINATION
13.1 Term. This Agreement shall commence on the Effective Date and shall
be in full force and effect until the expiration of the last to expire Royalty
Term or, if terminated earlier pursuant to Section 13.3 or Section 13.4, until
the effective date of termination as provided in Section 13.3 or Section 13.4
(the "TERM"). The Parties shall be obligated to continue to perform all of their
obligations, and enjoy all of their rights, under this Agreement until the end
of the Term.
13.2 Condition Precedent
(a) HSR Compliance. If required, each Party shall use Commercially
Diligent Efforts to satisfy any applicable requirements under the HSR, and the
regulations promulgated thereunder, including by making an initial HSR filing no
later than five (5) Business Days after the Execution Date. This Agreement will
not be
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effective until the date ("EFFECTIVE DATE") of either satisfaction of any such
requirements and the expiration or termination of all applicable waiting periods
(including any extensions thereof), or when AstraZeneca determines and notifies
AGIX in writing that no filings are required thereunder. All obligations,
rights, duties and liabilities under this Agreement (except those contained in
this Section and Sections 10, 14 and 15 of this Agreement) are subject to such
date.
(b) Cooperation. Each Party shall cooperate with the other Party in
the prompt preparation, execution and filing of all documents that are required
or permitted to be filed pursuant to HSR, and to notify the other Party upon
receipt of any formal or informal requests for information from any antitrust
agency in connection with any filings under HSR. Each Party shall bear its own
costs with respect thereto (including the filing fees for HSR, which shall be
paid by AstraZeneca).
(c) Termination Right. If the Effective Date has not occurred within
six (6) months after the Execution Date, notwithstanding that each Party having
fulfilled its obligations under this Section, either Party has the right to
terminate this Agreement without liability to the other Party by notice in
writing with immediate effect.
13.3 Termination by AstraZeneca
(a) ARISE
(i) The JDC shall determine, within five (5) days after
delivery by AGIX to the JDC of ARISE Results, whether such ARISE Results are
complete and final ("FINAL ARISE RESULTS"). If the JDC is unable to agree
unanimously as to whether such ARISE Results constitute Final ARISE Results
within such five (5) day period, the matter shall be immediately referred to the
JMC and, if the JMC cannot promptly resolve the matter, the officers set forth
in Section 14.1(b), or their designee, for attempted resolution by good faith
negotiations. In the event that the JMC and, if necessary, the designated
executive officers, do not resolve the matter within thirty (30) days, the ARISE
Results as submitted by AGIX shall for purposes of this Agreement be considered
Final ARISE Results.
(ii) AstraZeneca shall have the right, in its sole discretion
and for any reason, to terminate this Agreement in its entirety, upon ninety
(90) days' prior written notice, at any time during the [****] period following
the date the ARISE Results are determined to be Final ARISE Results as described
in section 13.3(a)(i).
(b) Approvable Letter. AstraZeneca shall have the right, in its sole
discretion and for any reason, to terminate this Agreement in its entirety, upon
ninety (90) days' prior written notice, at any time during the [****] period
following receipt of an Approvable Letter from the FDA if the Approvable Letter
specifies additional
-------
[****] indicates that certain confidential information contained in this
document has been omitted pursuant to a request for confidential treatment and
filed separately with the Securities and Exchange Commission.
75
information or materials required, or specified conditions, that are reasonably
likely to require, in order to obtain U.S. NDA Approval, either (i) more than
twenty-four (24) months from receipt of such Approvable Letter to submit such
additional information or materials to meet such condition, or (ii) reasonable
out-of-pocket costs paid to Third Parties (whether or not AstraZeneca were to
actually engage Third Parties for such activities or perform them internally) of
more than [****] by AstraZeneca for items or activities not included in the
Initial Development Plan, unless AGIX agrees to pay any amounts in excess of
such [****].
(c) Additional Studies. AstraZeneca shall have the right in its sole
discretion and for any reason, upon ninety (90) days' prior written notice, to
terminate this Agreement in its entirety if the FDA, in an Approvable Letter
subsequent to the Approvable Letter referred to in Section 13.3(b), requires
information or data from additional studies not contemplated in the Initial
Development Plan, where the reasonable out-of-pocket costs paid to Third Parties
(whether or not AstraZeneca were to actually engage Third Parties for such
activities or perform them internally) for such additional information or
studies, when added to the cost to AstraZeneca of complying with the
requirements described in Section 13.3(b), is reasonably likely to exceed
[****], unless AGIX agrees to pay any amounts in excess of such [****].
(d) Elective Termination. AstraZeneca shall have the right, in its
sole discretion and for any reason, to terminate this Agreement in its entirety,
at any time during the one-year period following the third annual anniversary of
receipt of U.S. NDA Approval, upon three hundred sixty-five (365) days' written
notice to AGIX delivered at any time during such one-year period.
13.4 Termination for Material Breach or Bankruptcy
(a) Breach. If a Party materially breaches any material term of this
Agreement, the other Party may terminate this Agreement or any part thereof as
specifically permitted by this Agreement, effective ninety (90) days after
providing written notice to the breaching Party (or, in the case of a breach of
the diligence obligation by AstraZeneca provided for in Section 5, one hundred
and eighty (180) days or, if the breach of the diligence obligations are
referred to arbitration under Section 14, as specified by the Arbitration Panel
under Section 14.4), if within that time the breaching Party fails to cure its
material breach and the non-breaching Party does not withdraw its termination
notice.
(b) Tolling of Time Periods. In the event that a Party initiates
arbitration proceedings pursuant to Section 14 during the ninety (90) day cure
period set forth in Section 13.4(a), such ninety (90) day period shall be
extended during the pendency of any dispute resolution proceedings under Section
14 (i.e., until the Arbitration Panel issues a final decision) with respect to
such termination notice.
-------
[****] indicates that certain confidential information contained in this
document has been omitted pursuant to a request for confidential treatment and
filed separately with the Securities and Exchange Commission.
76
(c) Bankruptcy. Either Party may terminate this Agreement if (i) the
other Party files in any court or agency pursuant to any statute or regulation
of any state or country, a petition in bankruptcy or insolvency or for
reorganization or for an arrangement or for the appointment of a receiver or
trustee of a Party or of its assets, (ii) the other Party proposes a written
agreement of composition or extension of its debts, (iii) the other Party is
served with an involuntary petition against it, filed in any insolvency
proceeding, and such petition is not dismissed within sixty (60) days after the
filing thereof, (iv) the other Party proposes or is a Party to any dissolution
or liquidation, or (v) the other Party makes an assignment for the benefit of
creditors.
13.5 Effects of Termination. If a Party terminates this Agreement under
Section 13.3 or 13.4, all terms and provisions shall terminate as of the
effective date of termination, except as otherwise expressly provided in this
Section 13.5 and in Section 13.7.
(a) AstraZeneca Elective Termination. If AstraZeneca terminates this
Agreement pursuant to Section 13.3(d):
(i) the provisions of Section 13.5(b) shall apply, except that
the license grants in Section 7 shall terminate throughout the Territory;
(ii) AstraZeneca shall pay to AGIX, on or before receipt by
AGIX of the written notice described in Section 13.3(d), a nonrefundable,
noncreditable payment, by immediately available funds via a Federal Reserve
electronic wire transfer to a bank designated by AGIX, of an amount of cash
equal to [****] Recent Monthly Net Sales; and
(iii) AstraZeneca shall, upon the execution of a note (the
documentation for which the Parties shall reasonably cooperate) to be held by
AstraZeneca and reasonably satisfactory to the Parties and, in no event later
than fifteen (15) days after receipt by AGIX of the written notice described in
Section 13.3(d), make an unsecured loan to AGIX, on an interest-free basis,
payable in full on or before the date that is thirty-six (36) months after the
date such loan is made (with no payments of principal required prior to
maturity), in an amount equal to [****] Recent Monthly Net Sales.
(b) Termination for AstraZeneca Breach or Bankruptcy or Termination
Pursuant to Sections 13.3(a)-(c). If AGIX terminates this Agreement pursuant to
Section 13.4 or if AstraZeneca terminates this Agreement pursuant to Section
13.3(a), 13.3(b) or 13.3(c):
-------
[****] indicates that certain confidential information contained in this
document has been omitted pursuant to a request for confidential treatment and
filed separately with the Securities and Exchange Commission.
77
(i) the Parties shall (A) pay any amounts due pursuant to this
Agreement prior to the date of termination; and (B) not enter into or incur, or
be required to enter or incur, any material obligations in furtherance of the
Development Plan or the Commercialization Plan without the written agreement of
the Parties following notice of termination;
(ii) AstraZeneca shall assign, or, in the case of (E) and (F)
license, and promptly transfer to AGIX, or its Affiliates as requested by AGIX,
and AGIX will assume and thereafter be fully responsible and liable for, at no
expense to AGIX or its Affiliates, all of AstraZeneca's right, title and
interest in and to:
(A) all Regulatory Materials, Regulatory Approvals, drug
master files and clinical trial agreements (to the extent assignable and
not cancelled) for Product(s) or Compound(s);
(B) all data, including clinical data, preclinical and
clinical study protocols, materials and information of any kind or nature
whatsoever, in AstraZeneca's possession or in the possession of its
Affiliates or its or their respective agents related to the Product(s) or
any Compound(s);
(C) all trademarks and product logos related to
Products;
(D) all information related to Commercialization of the
Product(s) or any Compound(s) including, but not limited to, market
development and pre-launch scientific awareness program plans, market
research studies, marketing plans, Promotional Materials, sales plans,
sales territory assignments, physician targeting, and call plans;
provided, however, that AGIX shall not use any Promotional Materials
containing AstraZeneca's name in connection with the sale of any
Product(s) or Compound(s) after the termination of this Agreement;
(E) all material information, and any other information
reasonably requested and required by AGIX, to the extent relating to the
Development, Manufacture or Commercialization of the Compound and/or
Products in the Field;
(F) if so elected by AGIX, AstraZeneca shall grant to
AGIX a license in all of AstraZeneca's interest in and to Joint Inventions
and Joint Patents necessary or useful for the Development, Manufacture or
Commercialization of the Compound and/or Products in the Field. In the
event of such election, the Parties shall negotiate in good faith
commercially reasonable terms for such license; provided, however, that
such license shall be effective upon the election whether or not the terms
have been negotiated and provided further that such license shall not
include any up-front fees or milestone payments unless both Parties agree.
If the Parties do not agree upon the terms of such
78
license after thirty (30) days of good faith negotiations, then either
Party may refer the issue to Arbitration in accordance with Section 14.
(iii) AstraZeneca shall return or provide to AGIX all
Compounds within its possession or control and arrange for the AstraZeneca
Sublicensees to return to AGIX all Compounds within such AstraZeneca
Sublicensees' possession or control;
(iv) all licenses granted by AstraZeneca to Sublicensees under
the rights granted pursuant to Section 7 shall terminate;
(v) AGIX shall revoke (and AstraZeneca shall allow revocation
of) any powers of attorney for any AGIX Compound Patents and Other AGIX Patents
that AstraZeneca holds as of the time of such termination;
(vi) Until such time, if at all, that AstraZeneca assigns this
Agreement and other assets to AGIX under Section 4.3 of the Transition Services
Agreement, AstraZeneca shall supply (or cause its Third Party manufacturers to
supply) Product(s) and/or Compound(s) to AGIX to the extent AstraZeneca had,
prior to such termination, been Manufacturing Product(s) and/or Compound(s) and,
at AGIX's request, shall assist in the transfer of Manufacturing processes to
new suppliers;
(vii) In the event that AstraZeneca supplies Product and/or
Licensed Compounds pursuant to Section 13.5(b)(vi), AGIX shall pay AstraZeneca
(A) its out-of-pocket costs, to the extent such Manufacture, transfer and
distribution activities are conducted by Third Parties and/or (B) a reasonable
market rate, to the extent that AstraZeneca conducts such Manufacture, transfer
and distribution activities. The Parties will cooperate to effect such transfer
as soon as practicable. In any event, AstraZeneca's obligations to transfer and
supply under Sections 13.5(b)(vi) shall expire two (2) years after such
termination;
(viii) AGIX may elect to acquire an exclusive, royalty bearing
license to intellectual property Controlled by AstraZeneca to the extent it is
incorporated into a Compound or Product or is necessary or useful for the
Manufacture thereof, with a right to sublicense, solely to develop, make, have
made, use, sell, have sold, offer for sale, and import such Compound or Product
in the Field in the Territory. In the event of such election, the Parties shall
negotiate in good faith commercially reasonable terms for such license;
provided, however, that such license shall not include any up-front fees or
milestone payments unless both Parties agree; provided further that after ninety
(90) days following such election either Party may seek Arbitration as to the
terms of such license under Article 14;
(ix) In the event that, at the time of termination, there is a
Combination Product in Development that contains an Exclusive Market Product, or
if such Combination Product has undergone a First Commercial Sale, the Parties
shall, in
79
good faith, negotiate an arrangement under which (i) the Parties shall jointly
Develop and Commercialize such Combination Product; (ii) each Party shall bear
its own costs associated with its Commercialization activities; (iii) each Party
shall share in the economic benefit of any such arrangement in accordance with
the relative contribution of such Party's compound(s); and (iv) each Party would
grant to the other Party a nonexclusive license to any intellectual property
rights necessary solely to permit the arrangements described in this Section
13.5(b)(ix); and
(x) In the event that, at the time of termination, there is a
Combination Product in Development that contains only a Non-Exclusive Market
Product, and no Exclusive Market Product, or if any such Combination Product has
undergone a First Commercial Sale, AGIX shall acquire all rights to such
Combination Product to the extent necessary and to the extent such rights are
not available from any Third Party, and the provisions of Section
13.5(b)(i)-(viii) shall apply to such Combination Product (including AGIX
acquiring from AstraZeneca any necessary licenses to intellectual property
Controlled by AstraZeneca).
(c) Termination for AGIX Breach or Bankruptcy. If AstraZeneca
terminates this Agreement pursuant to Section 13.4:
(i) The Parties shall pay any amounts due pursuant to this
Agreement prior to the date of termination.
(ii) AstraZeneca may elect to have all or any portion of the
licenses granted to AstraZeneca pursuant to Section 7 and all of the covenants
and obligations of AGIX, but not those of AstraZeneca, under Section 7 survive,
in which case AstraZeneca's obligations to AGIX under Section 8 shall survive to
the extent that AstraZeneca elects to retain any license grant hereunder.
(iii) AstraZeneca shall have no further obligations under
Section 5.2.
(iv) The obligations of the Parties under Sections 2, 3, 4, 5
and 6 shall expire.
(v) AGIX shall assign and promptly transfer to AstraZeneca, or
its Affiliates as requested by AstraZeneca, at no expense to AstraZeneca or its
Affiliates, all of AGIX's right, title and interest in and to: (A) all
Regulatory Materials, Regulatory Approvals, drug master files and clinical trial
agreements (to the extent assignable and not cancelled) for the Product(s) or
any Compounds; (B) all data, including clinical data, materials and information
of any kind or nature whatsoever, in AGIX's possession or in the possession of
its Affiliates or its or their respective agents related to the Product(s) or
any Compounds (in the event that such right, title and interest has not
previously been assigned). Furthermore, AGIX shall cooperate and provide to
AstraZeneca any powers
80
of attorney requested by AstraZeneca for Other AGIX Patents and AGIX Compound
Patents.
(vi) AstraZeneca may elect to have any agreements to which
AGIX is a party providing for Manufacturing services assigned to AstraZeneca, to
the extent permitted by such agreements.
(d) Post-Termination Assistance. Upon termination of this Agreement
due to breach or upon AstraZeneca terminating this Agreement pursuant to Section
13.3, the breaching Party or AstraZeneca, as the case may be, shall provide to
the other Party at no cost, such additional appropriate technology transfer,
transition assistance and post-termination services not otherwise specified in
this Section 13, including without limitation, Manufacturing services and the
continuation of the Supply of Product, necessary or useful for such other Party
to effectuate its rights hereunder.
(e) Return of Confidential Information. Upon expiration or
termination of this Agreement, the Parties shall comply with Section 10.1(b).
13.6 Non-Exclusive Rights. The foregoing rights and remedies of the
Parties set forth in Section 13.5 is non-exclusive and without prejudice to any
rights that either Party may have arising under applicable law or equity.
13.7 Rights in Bankruptcy. All rights and licenses granted under or
pursuant to this Agreement by AGIX and AstraZeneca are, and shall otherwise be
deemed to be, for purposes of Section 365(n) of the U.S. Bankruptcy Code,
licenses of rights to "Intellectual Property" as defined under Section 101 of
the U.S. Bankruptcy Code. The Parties agree that the Parties, as licensees of
such rights under this Agreement, shall retain and may fully exercise all of
their rights and elections under the U.S. Bankruptcy Code. The Parties further
agree that, in the event of the commencement of a bankruptcy proceeding by or
against a Party under the U.S. Bankruptcy Code, the Party hereto that is not a
Party to such proceeding shall be entitled to a complete duplicate of (or
complete access to, as appropriate) any such intellectual property and all
embodiments of such intellectual property, which, if not already in the
non-subject Party's possession, shall be promptly delivered to it (a) upon any
such commencement of a bankruptcy proceeding upon the non-subject Party's
written request therefor, unless the Party subject to such proceeding continues
to perform all of its obligations under this Agreement or (b) if not delivered
under clause (a) above, following the rejection of this Agreement by or on
behalf of the Party subject to such proceeding upon written request therefor by
the non-subject Party.
13.8 Accrued Rights and Obligations; Survival. Termination of this
Agreement by a Party pursuant to Section 13.4 shall not be a Party's sole remedy
for a material breach of this Agreement, but shall be in addition to any other
rights or remedies of a
81
Party under this Agreement. Termination or expiration of this Agreement shall
not affect any accrued rights or surviving obligations of the Parties. The
provisions of Sections 3.2(e), 9.1, 9.7(a), 10.1, 10.2, 11.10, 11.11, 13.1,
13.3, 13.4, 13.5, 13.6, 13.7, 13.8 and Sections 12, 14 and 15 shall survive the
expiration or termination of this Agreement for any reason whatsoever.
14. DISPUTE RESOLUTION
14.1 Procedure
(a) Scope. Any dispute arising out of or relating to this Agreement
(a "DISPUTE") is subject to the provisions of this Section 14; provided,
however, that Disputes regarding the scope, validity or enforceability of
Patents are excluded from the scope of this Section 14, ("Excluded Disputes")
and such Excluded Disputes shall be submitted to a court of competent
jurisdiction.
(b) Good Faith Negotiations. In the event of a Dispute that is not
an Excluded Dispute, either Party may provide written notice of the Dispute to
the other, in which event the Dispute shall be referred to the executive
officers designated below or their successors or designees, for attempted
resolution by good faith negotiations within fourteen (14) days after such
notice is received. Said designated officers are as follows:
For AGIX: President and Chief Executive Officer of AGIX
For AstraZeneca: Chief Executive Officer of AstraZeneca PLC In the
event the designated executive officers do not resolve such Dispute within the
allotted fourteen (14) days, either Party may within thirty (30) days of the end
of the fourteen (14) day period invoke the provisions of Section 14.2
hereinafter.
14.2 Alternative Dispute Resolution. Following the failure of settlement
efforts pursuant to Section 14.1, any Dispute other than an Excluded Dispute ,
shall be subject to binding arbitration ("ADR") in the manner described below:
(a) Request. A Party shall initiate an ADR to resolve a Dispute by
providing written notice (the "ADR REQUEST") to counsel for the other Party, the
issues to be resolved by the ADR.
(b) Issues Covered. Within ten (10) Business Days after the receipt
of the ADR Request, the other Party may, by written notice to the counsel for
the Party initiating ADR, add additional issues to be resolved, if such issues
had previously been addressed by the Executive Officers of the Parties pursuant
to Section 14.1. Issues that had not previously been addressed by the Executive
Officers of the Parties pursuant to Section 14.1, and issues not added within
(ten) 10 Business Days of receipt of the ADR
82
Request, may not be subjects of the ADR invoked by the ADR Request and must be
resolved, if at all, by initiation of separate Dispute proceedings.
14.3 Arbitration Procedure. The ADR shall be conducted pursuant to the
JAMS Rules then in effect, except that notwithstanding those rules, the
following provisions shall apply to the ADR hereunder:
(a) Panel. The arbitration shall be conducted by a panel of three
(3) arbitrators (the "ARBITRATION PANEL"). The Arbitration Panel shall be
selected from a pool of retired independent federal judges to be presented to
the Parties by JAMS.
(b) Process. The time periods set forth in the JAMS rules shall be
followed, unless a Party can demonstrate to the Arbitration Panel that the
complexity of the issues, urgency of the Dispute or other reasons warrant
extension or contraction of one or more of the timetables. For good cause shown,
the Arbitration Panel may extend or contract such timetables, but in no event
shall the timetables be extended so that the ADR proceeding extends more than
eighteen (18) months from the date of the ADR Request. Within such time frames,
each Party shall have the right to conduct such discovery as would be permitted
by the Federal Rules of Civil Procedure. The Arbitration Panel shall not award
punitive damages to either Party and the Parties shall be deemed to have waived
any right to such damages. The Arbitration Panel shall in rendering its
decision, apply the substantive law of the State of New York, excluding its
choice of law rules that would require the application of the laws of another
jurisdiction, except that the interpretation of and enforcement of this Section
14 shall be governed by the Federal Arbitration Act. The Arbitration Panel shall
apply the Federal Rules of Evidence to the hearing. In the event that
arbitration is initiated by AGIX, the hearing shall convene in New York, New
York. In the event that arbitration is initiated by AstraZeneca, the hearing
shall convene in Atlanta, Georgia. The fees of the Arbitration Panel and JAMS
shall be paid by the losing Party, which shall be designated by the Arbitration
Panel. If the Arbitration Panel is unable to designate a losing Party, it shall
so state and the fees shall be split equally between the Parties.
(c) Remedies. The Arbitration Panel is empowered to award any remedy
allowed by law or equity, including money damages, prejudgment interest and
attorneys' fees, and to grant final, or complete relief, but excluding punitive
damages. By agreeing to arbitration, the Parties do not intend to deprive any
court of its jurisdiction to issue a pre-arbitral injunction, pre-arbitral
attachment, or other order in aid of arbitration proceedings and the enforcement
of any award. Without prejudice to such provisional remedies as may be available
under the jurisdiction of a court, the Arbitration Panel shall have full
authority to grant provisional remedies (including without limitation injunctive
relief) or to order any Party or Parties to request that a court modify or
vacate any temporary or preliminary relief issued by that court, and to award
damages for the failure of any Party to comply with the Arbitration Panel's
orders to that effect.
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(d) Fees. Except as set forth in Section 14.3(b) above, each Party
shall bear its own legal fees and expenses against the Party losing the ADR
unless it believes that neither Party is the clear loser, in which case the
Arbitration Panel shall divide such fees, costs and expenses according to the
Arbitration Panel's sole discretion.
(e) Confidentiality. The ADR proceeding shall be confidential and
the Arbitration Panel shall issue appropriate protective orders to safeguard
each Party's Confidential Information. Except as required by law, no Party shall
make (or instruct the Arbitration Panel to make) any public announcement with
respect to the proceedings or decision of the Arbitration Panel without prior
written consent of each other Party. The existence of any Dispute submitted to
ADR, and the award, shall be kept in confidence by the Parties and the
Arbitration Panel, except as required in connection with the enforcement of such
award or as otherwise required by applicable law.
(f) Judicial Enforcement. The Parties agree that judgment on any
arbitral award issued pursuant to this Section shall be entered in the United
States District Court for the Northern District of Georgia.
(g) Governing Law. This Agreement shall be governed and construed in
accordance with the laws of the State of New York, except for any of its choice
of law rules that would require the application of the laws of another
jurisdiction.
14.4 Special Rules for Disputes Concerning Diligence Covenant. In
rendering any decision involving any Dispute relating to or arising out of
Section 5, the Arbitration Panel shall specify:
(a) the requirements, if any, considered necessary or appropriate
for a Party to comply with Section 5, and
(b) the deadline or deadlines for taking steps required for any such
compliance, which deadlines may be shorter or longer than the one hundred eighty
(180) day cure period specified in Section 13.4(a).
15. MISCELLANEOUS
15.1 Standstill. [****]
15.2 Termination of Certain Rights Upon AGIX Change of Corporate Control.
Notwithstanding anything else in this Agreement to the contrary, unless
otherwise specified by AstraZeneca within three (3) months after a Change of
Corporate Control involving AGIX, the following provisions of this Agreement
shall terminate:
-------
[****] indicates that certain confidential information contained in this
document has been omitted pursuant to a request for confidential treatment and
filed separately with the Securities and Exchange Commission.
84
(a) AGIX's right to participate in the JDC, JMC, Global
Commercialization Team, U.S. Commercialization Team, and any other subcommittees
or working groups established pursuant to Section 6.1, except as provided in
Section 15.2(b);
(b) AGIX and/or its successor shall continue to participate fully on
the IPC, except that the IPC shall no longer have decision-making jurisdiction
over all Licensed Patents, but instead shall have such jurisdiction only over
Other AGIX Patents, with AstraZeneca having unilateral control over Prosecution,
enforcement and defense of AGIX Compound Patents (and the rest of IPC
jurisdiction and control would remain unaffected);
(c) some or all of AGIX's rights as described in the Co-Promotion
Agreement, to the extent and as provided therein. The Co-Promotion Agreement
further provides that, under certain circumstances described herein, AstraZeneca
may, following an AGIX Change of Corporate Control, object under certain
circumstances to AGIX being permitted to continue to co-promote the Product; and
(d) AstraZeneca shall assume control of Prosecution, enforcement and
defense of all AGIX Compound Patents. AGIX shall cooperate in providing to
AstraZeneca all information, assistance, assignments and other support
reasonably requested to assist AstraZeneca in assuming such control.
15.3 Assignment. This Agreement shall inure to the benefit and be binding
upon each Party, its successors and assigns, except as provided in Section 15.2.
The Agreement may not be assigned or otherwise transferred, nor, except as
expressly provided hereunder, may any right or obligation hereunder be assigned
or transferred by either Party without the prior written consent of the other
Party, provided, however, that either Party may, without such consent, assign
the Agreement and its rights and obligations hereunder (i) to an Affiliate,
provided such Affiliate has the financial resources to perform the obligations
of this Agreement in the reasonable judgment of the other Party or (ii) in
connection with the transfer or sale of all or substantially all of its assets
or business to which this Agreement relates, or in the event of its merger or
consolidation or change in control or similar transaction, or a sale of all or
substantially all the pharmaceutical business assets of the Party; and provided
further, that AGIX or an Affiliate of AGIX shall be permitted to sell, assign or
transfer the right to receive Royalties owed by AstraZeneca to AGIX pursuant to
Section 8 to one or more Third Parties, and shall be permitted in connection
with any such sale, assignment or transfer, to assign the right to receive
reports and audit rights pursuant to Section 8, but not any other rights
hereunder, except to the extent the Parties otherwise agree in writing, to such
Third Party or Third Parties. Any attempted assignment not in accordance with
this Section 15.3 shall be void.
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15.4 Force Majeure. Neither Party shall be liable for any delay or failure
of performance to the extent such delay or failure is caused by circumstances
beyond its reasonable control and that by exercise of due diligence it is unable
to prevent, provided that the Party claiming excuse immediately notifies the
other Party and uses and continues to use commercially reasonable efforts to
overcome the same.
15.5 Further Assurances. The Parties intend that this Agreement contain
all consents, licenses and authorizations from one Party to the other necessary
to enable each Party to perform its obligations hereunder. In the event any
further such consents, licenses or authorizations are necessary, each Party
agrees to take such further actions and execute such further agreements as may
be reasonably necessary to carry out the intent and purposes of this Agreement.
15.6 Severability. The provisions of this Agreement are severable. If any
item or provision of this Agreement shall to any extent be invalid or
unenforceable, the remainder of this Agreement shall not be affected thereby,
and each term and provision of this Agreement shall be valid and shall be
enforced to the fullest extent permitted by law. The Parties will use diligent
good faith efforts to revise this Agreement as and to the extent reasonably
necessary to effectuate their original intent and purpose under this Agreement.
15.7 Notices. All notices hereunder shall be in writing and shall be
delivered personally, sent for next day delivery by internationally recognized
courier service or transmitted by facsimile (transmission confirmed), with
confirmation by next day delivery by an internationally recognized courier
service, to the following addresses and facsimiles of the respective Parties or
such other address or facsimile as is notified pursuant to this Section 15.7:
If to AGIX: AtheroGenics, Inc.
0000 Xxxxxxxx Xxxxxxx
Xxxxxxxxxx, Xxxxxxx 00000
Attn: President and Chief Executive Officer
Fax: (000) 000-0000
With a copy to: Xxxxxx & Xxxxxx LLP
Suite 900
0000 Xxxxxx Xxxxxxxxx
XxXxxx, Xxxxxxxx 00000
Attn: Xxxxx Xxxxxx, Esq.
Fax: (000) 000-0000
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If to AstraZeneca: IPR Pharmaceuticals, Inc.
XXXX 188 LOTE 00
XXX XXXXXX XXXXXXXXXX XXXX
XXXXXXXXX, XX 00000
Attn: President and General Manager
Fax: (000) 000-0000
With a copy to: Xxxxxx XxXxxxxxxxx, Senior Legal Counsel
AstraZeneca
Alderley House
Alderley Park
Macclesfield
Post Code XX00 0XX Xxxxxxx
15.8 Jurisdiction and Venue. In connection with any Dispute arising
hereunder or in connection with the subject matter hereof that is not settled in
accordance with Sections 14.1 and 14.2, each of the Parties hereby consents to
the non-exclusive jurisdiction and venue of the U.S. federal courts located
within the Southern District of New York. Each Party hereby irrevocably waives
any right that it may have to assert that any such court lacks jurisdiction,
other than the grounds that such Dispute is covered by Section 14, or that such
forum is not convenient.
15.9 Affiliates. Without limiting the generality of the foregoing, any
obligations of AstraZeneca may be performed by any of AstraZeneca's Affiliates,
including but not limited to AstraZeneca, and such obligations will be deemed
satisfied upon full and complete performance by such Affiliate as specified in
this Agreement.
15.10 Entire Agreement. This Agreement and the Related Agreements, herein
and therein, including any exhibits expressly named and referenced herein and
therein, constitute the entire agreement and understanding of the Parties and
supersede any prior agreements or understandings relating to the subject matter
hereof, including the Confidential Disclosure Agreement between AGIX and
AstraZeneca Pharmaceuticals LP dated as of March 12, 2003. Any modification of
this Agreement shall be effective only to the extent it is reduced to writing
and signed by a duly authorized representative of each Party hereto.
15.11 Headings. The captions to the several Sections and subsections
hereof are not a part of this Agreement, but are merely for convenience to
assist in locating and reading the several Articles and Sections hereof.
15.12 Independent Contractors. It is expressly agreed that AGIX and
AstraZeneca shall be independent contractors and that the relationship between
the two
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Parties shall not constitute a partnership, joint venture or agency. Neither
AGIX nor AstraZeneca shall have the authority to make any statements,
representations or commitments of any kind, or to take any action, which shall
be binding on the other, without the prior consent of the other Party.
15.13 Waiver. The failure on the part of a Party to exercise or enforce
any rights conferred upon it hereunder shall not be deemed to be a waiver of any
such rights nor operate to bar the exercise or enforcement thereof at any time
or times hereafter.
15.14 No Third Party Beneficiaries. This Agreement is neither expressly
nor impliedly made for the benefit of any Person other than the Parties.
15.15 Cumulative Remedies. No remedy referred to in this Agreement is
intended to be exclusive, but each shall be cumulative and in addition to any
other remedy referred to in this Agreement or otherwise available under law.
15.16 Counterparts. The Agreement may be executed in two or more
counterparts, each of which shall be deemed an original, but all of which
together shall constitute one and the same instrument.
15.17 Waiver of Rule of Construction. Each Party has had the opportunity
to consult with counsel in connection with the review, drafting and negotiation
of this Agreement. Accordingly, the rule of construction that any ambiguity in
this Agreement shall be construed against the drafting Party shall not apply.
END OF PAGE
(signatures appear on following page)
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IN WITNESS WHEREOF, the Parties have executed this Agreement as of the
Effective Date.
ATHEROGENICS, INC. IPR PHARMACEUTICALS, INC.
By /s/ XXXXXXX X. XXXXXXX By /s/ XXXXX XXXXXX
--------------------------------- -------------------------------
Name: Xxxxxxx X. Xxxxxxx M.D., Ph.D. Name: Xxxxx Xxxxxx
Title: President & CEO Title: President & General Manager
