EXHIBIT 10.11
COLLABORATION
AGREEMENT
"BIOCOR"
THIS COLLABORATION AGREEMENT effective as of this 12th day of February,
1998 (the "Collaboration Date"), is made by and between VERSICOR INC., a
Delaware corporation having its principal place of business at 00000 Xxxxxxxxx
Xxxxx, Xxxxxxx, Xxxxxxxxxx 00000 ("Versicor") and BIOSEARCH ITALIA, S.P.A., all
Italian corporation having its principal place of business at xxx X.Xxxxxxx 00,
00000 Xxxxxxxxx (Varese), ("Biosearch").
RECITALS
WHEREAS, Versicor has expertise in combinatorial chemical library synthesis
and in high throughput compound library screening techniques for relevant
biological activity for improvement and optimization of chemical compounds in
drug discovery programs;
WHEREAS, Biosearch owns or has rights to certain potential anti-bacterial
lead compounds derived from naturally occurring biological materials;
WHEREAS, Versicor and Biosearch wish to collaborate in the optimization
development of such Biosearch lead compounds as therapeutic pharmaceuticals;
WHEREAS, Versicor and Biosearch desire to enter into this Collaboration
Agreement which sets forth the principal terms of such collaborative
relationship, which the Parties refer to as "Biocor."
NOW, THEREFORE, in consideration of the foregoing premises and of the
covenants, and agreements contained in this Collaboration Agreement, Versicor
and Biosearch agree as follows:
ARTICLE 1
DEFINITIONS
When used in this Agreement, the following capitalized terms shall have the
meanings set forth below:
1.1 "ABANDONED LEAD" shall have the meaning set forth in Section 2.3.
1.2 "ANIMAL STUDIES" means the initial studies of the efficacy/toxicity of
an Optimized Compound in an animal model selected by the JLDC.
1.3 "BIOSEARCH LEAD COMPOUNDS" means those lead compounds owned or
controlled (with the right to license) by Biosearch set forth on Schedule 1.3
hereto, including molecular scaffolds derived by Biosearch from such lead
compounds. "Biosearch Lead Compounds" shall also include lead compounds (and
molecular scaffolds derived therefrom) discovered or acquired by Biosearch after
the Collaboration Date, except where the only suitable
1.
method of modification or optimization of such compounds into a drug candidate
consists of a routine, serial solution chemistry method. Schedule 1.3 shall be
updated from time to time to reflect the addition of any such additional
Biosearch Lead Compounds.
1.4 "BIOSEARCH INVENTIONS" shall have the meaning set forth in Section 8.1.
1.5 "BIOSEARCH PATENT RIGHTS" means Patent Rights claiming (i) any
Biosearch Lead Compounds or Biosearch Technology; or (ii) any Biosearch
Invention or Joint Invention.
1.6 "BIOSEARCH TECHNOLOGY" means information or technology owned, acquired,
developed, or controlled by Biosearch (with the right to license) as of the
Collaboration Date or during the Development Program Term, which relates to the
biological or chemical properties of Biosearch Lead Compounds or is otherwise
useful in the conduct of the Compound Development Plan.
1.7 "BIOSEARCH TERRITORY" means the areas reserved for Biosearch's
exclusive commercialization of Hospital Products. Specifically, Biosearch
Territory shall mean the countries of Europe.
1.8 "COMPOUND DEVELOPMENT PLAN" shall have the meaning set forth in Section
2.1.
1.9 "CONFIDENTIAL INFORMATION" means, as to a Party hereto, all of that
Party's confidential information, data, or know-how disclosed by that Party
pursuant to this Collaboration Agreement, whether in oral, written or electronic
form.
1.10 "CORE DOSSIER" means the dossier of common human clinical trial data
and regulatory information required for filing for regulatory approval in both
the Biosearch Territory and the Versicor Territory.
1.11 "CORPORATE PARTNERING REVENUE" means any and all (i) up-front,
milestone and other cash payments; (ii) royalty payments, or (iii) profit share
payments owed in consideration for the license to a Third Party of (a) a Primary
Care Product anywhere in the world; or (b) or a Hospital Product in the Joint
Territory. In no event shall Corporate Partnering Revenue include payments made
by such Third Party for equity in or a loan to either Party, or for the
sponsorship of research or development activities to be performed by such Party,
but Corporate Partnering Revenue shall include the fair market value of any
non-cash asset received from such Third Party.
1.12 "DEVELOPMENT PROGRAM TERM" means the period commencing on the
Collaboration Date and ending on the fifth anniversary of the Collaboration
Date, subject to extension by mutual agreement of the Parties.
1.13 "HOSPITAL PRODUCT" means a Product in an intravenous formulation for
administration primarily in an inpatient setting, such as hospitals or clinics.
1.14 "IND" means an Investigational New Drug application filed with the
United States Food and Drug Administration ("FDA"), or its equivalent or any
corresponding application filed in any country other than the United States.
2.
1.15 "JOINT INVENTION" shall mean the meaning set forth in Section 8.1.
1.16 "JOINT LEAD DEVELOPMENT COMMITTEE" or "JDLC" shall have the meaning
set forth in Section 3.1.
1.17 "JOINT MANAGEMENT COMMITTEE" or "JMC" shall have the meaning set forth
in Section 3.3.
1.18 "JOINT TERRITORY" means all countries of the world other than the
Biosearch Territory and the Versicor Territory.
1.19 "NET SALES" shall mean the gross invoice sales of Hospital Product
sold to a Third Party less the following deductions:
(a) Trade, cash, and quantity discounts actually allowed and taken
directly with respect to such sales;
(b) Tariffs, duties, excises, sales taxes or other taxes imposed upon
and paid directly with respect to such sales (excluding national, state or local
taxes based on income);
(c) Amounts repaid or credited by reason of rejections, defects,
recalls or returns or because of rebates or retroactive price reductions; and
(d) One percent (1%) of Net Sales as an allowance to cover all other
items, such as freight, transportation and insurance.
Such amounts shall be determined from the books and records of the Party, its
Affiliates and/or its licensees or sublicensees, maintained in accordance with
generally accepted accounting principles, consistently applied.
1.20 "OPTIMIZED COMPOUND" means any Biosearch Lead Compound selected by the
JMC as a candidate for Animal Studies, and possibly additional preclinical and
clinical studies.
1.21 "PARTY" means Versicor or Biosearch.
1.22 "PATENT RIGHTS" mean patents, patent applications, certificates of
invention, or applications for certificates of invention, divisions,
continuations, continuations-in-part, reissues, reexaminations, extensions, and
foreign counterparts thereof.
1.23 "PRIMARY CARE PRODUCT" means a Product in an oral formulation for
administration primarily in an out patient setting, such as by primary care
physicians.
1.24 "PRODUCT" means any pharmaceutical product, in any formulation, the
active ingredient of which is an Optimized Compound.
1.25 "TECHNOLOGY" means inventions, trade secrets, processes, algorithms,
know-how, data, databases, software, and other technology of any kind, including
any proprietary biological material, compounds, or reagents.
3.
1.26 "THIRD PARTY" means any entity other than Versicor and Biosearch.
1.27 "VERSICOR INVENTIONS" shall have the meaning set forth in Section 8.1.
1.28 "VERSICOR PATENT RIGHTS" means Patent Rights claiming (i) any Versicor
Technology, or (ii) any Versicor Inventions or Joint Inventions.
1.29 "VERSICOR TECHNOLOGY" means all Technology owned or controlled by
Versicor relating to or useful in the development of Optimized Compounds.
1.30 "VERSICOR TERRITORY" means the areas designated for Versicor's
exclusive commercialization of Hospital Products. Specifically, Versicor
Territory shall mean the United States and Canada.
ARTICLE 2
SCOPE OF COMPOUND
DEVELOPMENT COLLABORATION
2.1 SCOPE; COMPOUND DEVELOPMENT PLAN. Versicor and Biosearch agree to
collaborate in the optimization and evaluation of the Biosearch Lead Compounds
and development of Optimized Compound(s). Such collaboration will be conducted
pursuant to a Compound Development Plan, an initial outline of which is attached
to this Collaboration Agreement as Schedule 2.1. Each of the Parties will be
responsible for the conduct of those portions of the Compound Development Plan
allocated to it thereunder.
2.2 RESPONSIBILITIES OF THE PARTIES.
(a) BIOSEARCH RESPONSIBILITIES. Biosearch shall initially provide to
Versicor each of the Biosearch Lead Compounds in quantities sufficient for
Versicor's use under the six (6) month evaluation time period. Biosearch shall
also provide to Versicor any Biosearch Technology relevant to such Biosearch
Lead Compound. Upon return to Biosearch of any Optimized Compounds, Biosearch
shall be responsible for their IN VIVO characterization in the Animal Studies.
Biosearch shall also be responsible for the supply to Versicor of any
preclinical materials needed for the conduct of the Compound Development Plan,
as set forth in Article 6 below.
(b) VERSICOR RESPONSIBILITIES. Versicor shall, upon receipt of a given
Biosearch Lead Compound, have a period of six (6) months to evaluate such
Biosearch Lead Compound to determine whether, in Versicor's good faith
scientific judgment, such Biosearch Lead Compound is amenable to improvement,
optimization or modification by Versicor using the Versicor Technology. If
Versicor determines that such Biosearch Lead Compound is so amenable, it shall
notify the JLDC, and Versicor shall have an additional period of no more than
eighteen (18) months in which to conduct Versicor Studies, followed by, where
appropriate, high throughout screening and combinatorial synthesis with respect
thereto (collectively the "Versicor Studies.") The Versicor Studies shall be
performed in an effort to identify and synthesize and present to the JLDC one or
more improved, enhanced or optimized compounds derived from the Biosearch Lead
Compound at issue, and appropriate for Animal Studies (an "Optimized
4.
Compound"). Versicor shall present to the JLDC the results of its studies; on
each Biosearch Lead Compound and all Optimized Compounds. After approval by the
JMC of a Biosearch Lead Compound as an Optimized Compound, Biosearch shall
conduct Animal Studies on such Optimized Compound.
(c) JOINT RESPONSIBILITIES. Each Party shall be responsible for all
costs associated with its activities under the Compound Development Plan, unless
otherwise specified in this Agreement. In addition, in carrying out the Compound
Development Plan, and as appropriate, Biosearch and Versicor shall furnish to
one another and to the JLDC written reports concerning each Party's respective
data and describe progress under the Compound Development Plan.
2.3 ABANDONMENT OF BIOSEARCH LEAD COMPOUND OR OPTIMIZED COMPOUND. If
Versicor determines not to proceed with Versicor Studies of any Biosearch Lead
Compound, or the JMC decides to abandon the development of any Optimized
Compound prior to the initiation of Animal Studies, then the Optimized Compound
or Biosearch Lead Compound, and all rights related thereto, shall be returned to
Biosearch and designated an "Abandoned Lead." Thereafter, Biosearch may
independently, or with a Third Party, conduct research, analysis, and
development of such Abandoned Lead without payment to Versicor.
2.4 EXCLUSIVITY. During the six (6) month period in which Versicor is
evaluating a Biosearch Lead Compound under Section 2.2(b), Biosearch agrees that
it shall not transfer, license, sell or otherwise provide such Biosearch Lead
Compound to any Third Party for any use. If any Biosearch Lead Compound is
selected by Versicor for Versicor Studies under Section 2.2 (b), Biosearch
agrees that it shall not transfer, license, sell or otherwise provide such
Biosearch Lead Compound to any Third Party unless and until the date any such
Biosearch Lead Compound is returned to Biosearch as an Abandoned Compound under
Section 2.3.
2.5 PAYMENTS TO BIOSEARCH. In consideration for the exclusivity obligation
set forth in Section 2.4 above, as well as the contribution to the collaboration
of the Biosearch Lead Compounds, Versicor agrees to pay to Biosearch the
following amounts with respect to each Optimized Compound:
(a) [ * ] upon the conclusion of Animal Studies of an Optimized
Compound, where the results of such Animal Studies successfully meet the
requirements specified by the JMC; and
(b) [ * ] upon the enrollment of the first patient in the first
Phase I clinical trials conducted with respect to such Optimized Compound,
anywhere in the world.
Notwithstanding the foregoing, Biosearch agrees that in the event the
"Licensed Product" as defined in and licensed to Versicor pursuant to that
certain License Agreement between Versicor and Biosearch dated as of the
Collaboration Date (the "License Agreement") becomes subject to this
Agreement as a Biosearch Lead Compound pursuant to Section 5.8 of the License
Agreement, no payments under this Section 2.5 will be owing by Versicor with
respect to such Biosearch Lead Compound.
[ * ] = CERTAIN CONFIDENTIAL INFORMATION CONTAINED IN THIS DOCUMENT, MARKED BY
BRACKETS, HAS BEEN OMITTED AND FILED SEPARATELY WITH THE SECURITIES AND
EXCHANGE COMMISSION PURSUANT TO RULE 406 OF THE SECURITIES ACT OF 1933, AS
AMENDED.
5.
ARTICLE 3
COLLABORATION GOVERNANCE
3.1 JOINT LEAD DEVELOPMENT COMMITTEE. Promptly after the Collaboration
Date, the Parties shall establish a Joint Lead Development Committee (JLDC) to
oversee and direct the Compound Development Plan. The JLDC will be composed of
three representatives appointed by Versicor and three representatives appointed
by Biosearch, in each Party's sole discretion. One of the Versicor
representatives will act as Chairman of the JLDC for the initial year of the
collaboration; such Chairmanship shall alternate thereafter on a yearly basis
with a Biosearch representative. Versicor and Biosearch each shall bear all
expenses of their respective members related to their participation on the JLDC.
All decisions of the JLDC shall be unanimous. The Chairman shall have the same
voting rights as each other member of the JLDC. Any disputes arising in the JLDC
shall be referred to the JMC for resolution.
(a) RESPONSIBILITIES OF THE JLDC. The responsibilities of the JLDC
will include, but are not limited to, the following:
(i) To prepare, update, evaluate, and modify, as necessary, the
Compound Development Plan;
(ii) To coordinate the activities of the Parties in the conduct
of the Compound Development Plan;
(iii) To recommend to the JMC, for its approval, any Biosearch
Lead Compound as an Optimized Compound; and
(iv) To provide scientific direction to the collaboration.
(b) MEETINGS OF THE JLDC. The JLDC shall meet at least quarterly, and
at such additional times as the Parties deem appropriate. For a quorum, at least
two representatives of each of Versicor and Biosearch shall be in attendance at
any meeting of the JLDC. The JLDC shall alternate the meetings between
Versicor's and Biosearch's business location, or as otherwise agreed to by the
Parties.
3.2 JOINT MANAGEMENT COMMITTEE. Promptly following the Collaboration Date,
the Parties Shall also establish a Joint Management Committee (JMC) to oversee,
manage and/or coordinate the preclinical and clinical development, manufacture,
and, in the Joint Territory, commercialization, of any Optimized Compound. The
Joint Management Committee will be composed of three representatives appointed
by Versicor and three representatives appointed by Biosearch, in each Party's
sole discretion. One of the Biosearch representatives will act as Chairman of
the JMC for the initial year of the collaboration; such Chairmanship shall
thereafter alternate on a yearly basis with a representative of Versicor.
Versicor and Biosearch each shall bear all expenses of their respective members
related to their participation on the JMC. All decisions of the JMC shall be
unanimous. The Chairman shall have the same voting rights as each other member
of the JMC. Should a disagreement arise in the JMC or the JMC be unable to
6.
come to consensus with respect to a given matter, the Parties shall proceed in
accordance with Section 14.3.
(a) RESPONSIBILITIES. The JMC shall include, without limitation, the
following responsibilities:
(i) To settle disputes or disagreements arising in the JLDC;
(ii) To designate a Biosearch Lead Compound as an Optimized
Compound;
(iii) To pursue further preclinical and clinical development of
an Optimized Compound;
(iv) To identify and evaluate potential Third Party licensees for
development and/or commercialization of Hospital Products within the
Joint Territory and Primary Care Products anywhere in the world, and
to appoint one Party as the lead negotiator therefor.
(b) MEETINGS OF THE JMC. Once established the JMC shall meet at least
semi-annually, or more often, in the reasonable judgment of the members of the
JMC. For a quorum, at least two representations of each of Versicor and
Biosearch shall be in attendance at any meeting of the JMC. The JMC shall
alternate the locations of the meetings between Versicor and Biosearch, or as
otherwise agreed to by the Parties.
ARTICLE 4
PRECLINICAL AND CLINICAL DEVELOPMENT OF PRODUCTS
4.1 LATER STAGE ANIMAL STUDIES. In the event of a decision by the JMC to
conduct later stage animal studies required for regulatory approval of an
Optimized Compound, the Parties shall share equally the costs associated with
such Animal Studies.
4.2 HOSPITAL PRODUCTS IN VERSICOR TERRITORY AND BIOSEARCH TERRITORY.
(a) CO-DEVELOPMENT. In the event the Parties determine to pursue
additional preclinical and clinical testing of a Hospital Product for the same
indication and in reasonably similar time frames, the Parties shall co-develop
such Hospital Product to the extent feasible. In such event, the Parties shall
share equally all costs associated with any preclinical studies required for the
filing of an IND in both the Biosearch Territory and the Versicor Territory, as
well as all costs associated with the conduct of all human clinical trials
needed to compile the Core Dossier. Each Party shall be responsible for all
costs associated with any other human clinical trials that are incremental to
those in the Core Dossier and required for regulatory approval only in the
Biosearch Territory, in the case of Biosearch, or in the Versicor Territory, in
the case of Versicor. The Parties shall jointly own all data in the Core
Dossier.
(b) UNILATERAL DEVELOPMENT. In the event the Parties do not determine
to co-develop a Hospital Product as provided in Section 4.2(a), each Party shall
be responsible for all
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costs associated with any other preclinical trials other than the Animal
Studies, and for all human clinical trials that are required for regulatory
approval in the Biosearch Territory, in the case of Biosearch, and in the
Versicor Territory, in the case of Versicor.
4.3 HOSPITAL PRODUCTS IN JOINT TERRITORY; PRIMARY CARE PRODUCTS WORLDWIDE.
(a) LICENSING TO THIRD PARTIES. It is the intention of the Parties to
license human clinical development and commercialization of (i) any Hospital
Product in the Joint Territory; and (ii) any Primary Care Product worldwide, to
a Third Party, with such Third Party licensee paying all costs related to such
development and commercialization. In order to facilitate the negotiation of
such license, with respect to the initial Primary Care Product or Hospital
Product in the Joint Territory, the JMC shall appoint one Party the lead
negotiator ("Lead Negotiator"). The Party not selected by the JMC shall be the
lead negotiator with respect to the Second Primary Care Product or Hospital
Product for the Joint Territory, and the Parties will alternate as lead
negotiator for each Primary Care Product or Hospital Product for the Joint
Territory developed thereafter. It is the intention of the Parties that the Lead
Negotiator be responsible for leading and coordinating the negotiations between
the two Parties, on the one hand, and the Third Party, and will not have the
right to act as agent on behalf of the other Party.
(b) COSTS. The Parties will share equally all costs associated with
the preclinical testing of, and obtaining any IND for, any Hospital Product and
Primary Product to be licensed to a Third Party under this Section 4.3, where
determined appropriate by the JMC. In the event the Parties are unable to
license either a Primary Care Product or a Hospital Product prior to the conduct
of Phase I clinical trials, and if the JMC determines that further development
of such Product is nonetheless worth pursuing, the Parties shall equally share
all costs associated with Phase I or later clinical trials, unless and until one
or the other Party elects to exercise its option to discontinue, as set forth in
Section 4.4.
4.4 OPTION TO DISCONTINUE INVESTMENT. The Parties each have the option to
discontinue participating in development of an Optimized Compound under Section
4.3(b) at each of the participating stages listed in the table below. If one
Party discontinues investing in an Optimized Compound and the other Party
continues to invest by completing the next stage unilaterally, the percentage of
Corporate Partnering Revenue due the non-participating Party under Section 5.3
shall be adjusted, based upon the stage at which the non-participating Party
elected to discontinue participating. The Party so electing to discontinue
participation shall notify the other Party in writing of its decision prior to.
8.
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SHARE OF CORPORATE PARTNERING REVENUE
--------------------------------------------------------------------------------
NON-INVESTING INVESTING
INVESTMENT STAGE PARTY SHARE (%) PARTY SHARE (%)
--------------------------------------------------------------------------------
Commencement of
Phase I Trials 25% 75%
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Commencement of
Phase II Trials 35% 65%
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In the event both Parties elect to discontinue participating in the development
of an Optimized Compound and neither Party elects unilaterally to continue to
conduct development, such Optimized Compound shall be deemed a Biosearch Lead
Compound and shall be subject again to the efforts of Versicor to optimize such
compound as set forth in Article 2.
ARTICLE 5
COMMERCIALIZATION
5.1 COMMERCIALIZATION OF HOSPITAL PRODUCTS IN BIOSEARCH TERRITORY.
Biosearch shall have the exclusive right to commercialize, market and sell
Hospital Products in the Biosearch Territory, either alone or in concert with a
Third Party. Biosearch shall be responsible for all costs associated with such
commercialization activities. Biosearch shall retain all income derived from
such commercialization activities in the Biosearch Territory.
5.2 COMMERCIALIZATION OF HOSPITAL PRODUCTS IN VERSICOR TERRITORY. Versicor
shall have the exclusive right to commercialize, market and sell Hospital
Products in the Versicor Territory, either alone or in concert with a Third
Party. Versicor shall be responsible for all costs associated with such
commercialization activities. Versicor shall retain all income derived from such
commercialization activities in the Versicor Territory.
5.3 COMMERCIALIZATION OF PRIMARY CARE PRODUCTS WORLDWIDE AND HOSPITAL
PRODUCTS IN JOINT TERRITORY. The Parties shall equally share all Corporate
Partnering Revenue derived from the development and commercialization of (i)
Hospital Products in the Joint Territory; and (ii) Primary Care Products
worldwide.
ARTICLE 6
MANUFACTURE AND SUPPLY
6.1 BIOSEARCH MANUFACTURING FACILITY; RIGHTS. The Parties acknowledge that
it is Biosearch's intention to establish a U.S. FDA approved manufacturing
facility for both the bulk as well as finished Hospital Product, at its own
expense. In the event Biosearch establishes such
9.
manufacturing facility in the appropriate time frame, it shall have the right to
manufacture all of its own as well as Versicor's requirements for preclinical,
clinical and commercial quantities. Biosearch shall also have the right to
manufacture all requirements for Optimized Compound and finished Hospital
Product in the Joint Territory. Such right to manufacture and supply, as it
applies to Phase III clinical supplies and commercial supplies, is contingent
upon Biosearch having established such manufacturing site in the agreed upon
time frame and its ability to supply at the price referenced in Section 6.2.
Should Biosearch not be able to establish such manufacturing facility, or not be
able to supply at such price, Versicor shall have the right to contract with a
Third Party for the manufacture and supply of its requirements of Hospital
Product for sale in the Versicor Territory and Biosearch shall transfer to such
Third Party all existing manufacturing know-how for such manufacture at a price
equal to two percent (2%) of Versicor's annual Net Sales of such Hospital
Product for a period of ten (10) years from the first commercial sale of such
Hospital Product.
6.2 SUPPLY AGREEMENT. Biosearch shall have the first right to supply to
Versicor its finished Hospital Product requirements pursuant to a supply
agreement to be entered into by the Parties following the Collaboration Date.
The price for finished Hospital Product shall be not greater than fifteen
percent (15%) of Versicor's Net Sales of such Hospital Product, but not less
than the price which Versicor would be required to pay any Third Party supplier.
The price for pre-clinical and clinical supplies needed after the six (6) month
evaluation period referred to in Section 2.2(b) shall be at Biosearch's actual
cost and shall be shared by the Parties.
ARTICLE 7
LICENSE GRANTS
7.1 Versicor grants to Biosearch the exclusive right and license, with the
right to sublicense, under the Versicor Patent Rights to (i) manufacture
Products and (ii) develop Optimized Compounds and use, import, offer for sale
and sell Hospital Products in the Biosearch Territory, pursuant to this
Agreement.
7.2 Biosearch grants to Versicor the exclusive rights and license, with the
right to sublicense, under the Biosearch Patent Rights to develop Optimized
Compounds and use, import, offer for sale and sell Hospital Products in the
Versicor Territory, pursuant to this Agreement.
7.3 Each Party agrees to license its rights to develop, use and sell any
Optimized Compound and use, import, offer for sale and sell (i) Hospital
Products in the Joint Territory and (ii) Primary Care Products worldwide, to
such Third Party licensee as is selected by the JMC.
ARTICLE 8
INTELLECTUAL PROPERTY RIGHTS
8.1 OWNERSHIP OF DISCOVERIES AND IMPROVEMENTS. Ownership of all inventions,
discoveries, improvements, and other technology, except for any manufacturing
processes and related improvements, whether or not patentable, and any patent
applications or patents based thereon (collectively, the "Inventions") that are
discovered, made or conceived during and in
10.
connection with the Definitive Collaboration Agreement shall be governed by this
Section 8.1. All Inventions coveting or relating to the development, use or sale
of Products in the Versicor Territory shall be owned by Versicor ("Versicor
Inventions"). All right, title and interest in all Inventions coveting or
relating to the development, use or sale of Products in the Biosearch Territory
shall be owned by Biosearch ("Biosearch Inventions"). Versicor and Biosearch
shall jointly own all right, title, and interest in all Inventions coveting or
relating to the development, use or sale of Products in the Joint Territory
("Joint Inventions"). Each of Versicor and Biosearch shall promptly disclose to
the JLDC the making, conception or reduction to practice of Inventions by
employees or others acting on behalf of such Party. Versicor shall make all
decisions concerning, and shall have full responsibility for, the preparation,
filing, prosecution and maintenance of patents coveting Versicor Inventions in
the Versicor Territory at its own cost. Biosearch shall make all decisions
concerning, and shall have full responsibility for, the preparation, filing,
prosecution and maintenance of patents coveting Biosearch Inventions in the
Biosearch Territory at its own cost. The JLDC shall make all decisions
concerning the preparation, filing, prosecution, and maintenance of patents
covering Joint Inventions in the Joint Territory and shall assign to either or
both parties the responsibility therefor. All costs associated with the
preparation, filing, prosecution and maintenance of patents concerning Joint
Inventions shall be equally shared.
8.2 PATENT ENFORCEMENT. If either party becomes aware that a patent
coveting a Versicor Invention or a Biosearch Invention is being infringed by a
Third Party in any country, that party shall promptly notify the other party in
writing. Versicor shall have the primary right, but not the obligation, to bring
and prosecute at its own expense an action concerning such infringement of a
Versicor Invention patent. Biosearch shall have the primary right, but not the
obligation, to bring and prosecute at its own expense an action concerning such
infringement of a Biosearch Invention patent. Any monetary award granted to the
prosecuting party hereunder shall be applied first to the costs and expenses of
the party prosecuting the action, then to the costs and expenses of the other
party. The party bringing the suit shall be entitled to any monetary awards in
excess of such amounts. The Parties shall confer with respect to the enforcement
of any patent covering a Joint Invention in the Joint Territory, and the way in
which any award should be allocated between the Parties. The Parties shall
cooperate with each other in connection with any action brought under this
Section 8.2.
8.3 DEFENSE AND SETTLEMENT OF THIRD PARTY CLAIMS. If a third party asserts
that a patent or other right owned by it is infringed by the research,
development, use, marketing, distribution, importation, offer for sale or sale
of any Hospital Product by Versicor in the Versicor Territory or by Biosearch in
the Biosearch Territory, Versicor or Biosearch, respectively, shall by
responsible for defending against any such assertions at its own costs.
ARTICLE 9
CONFIDENTIALITY
9.1 CONFIDENTIAL INFORMATION. No Confidential Information disclosed by one
Party to the other during the term of this Collaboration Agreement shall be used
by the receiving Party except in compliance with the rights and licenses granted
hereunder. Such Confidential Information shall be maintained in confidence by
the receiving Party (except to the extent
11.
reasonably necessary for regulatory approval of Products developed by either
Party), and shall not otherwise be disclosed by the receiving Party to any other
person, firm, or agency, governmental or private, without the prior written
consent of the disclosing Party, except to the extent that the Confidential
Information:
(a) was known or used by the receiving Party prior to its date of
disclosure to the receiving Party; or
(b) either before or after the date of the disclosure to the receiving
Party is lawfully disclosed to the receiving Party by sources other than the
disclosing Party rightfully in possession of the Confidential Information; or
(c) either before or after the date of the disclosure to the receiving
Party becomes published or generally known to the public, other than through the
sale of Products in the ordinary course, through no fault or omission on the
part of the receiving Party or its sublicensees; or
(d) is independently developed by or for the receiving Party without
reference to or reliance upon the Confidential Information; or
(e) is required to be disclosed by the receiving Party to comply with
applicable laws, to defend or prosecute litigation or to comply with
governmental regulations, provided that, the receiving Party provides prior
written notice of such disclosure to the other Party and takes reasonable and
lawful actions to avoid and/or minimize the degree of such disclosure.
9.2 EMPLOYEE OBLIGATIONS. Each of the Parties agrees to provide
Confidential Information received from the other Party only to such Party's
employees, consultants, and advisors who have a need to know and have an
obligation to treat such information and materials as confidential.
9.3 TERM. All obligations of confidentiality imposed under this Article 9
shall expire five (5) years following expiration or termination of this
Agreement.
12.
ARTICLE 10
PUBLIC ANNOUNCEMENTS
The content and timing of any announcements or similar publicity with
respect to the execution of this Collaboration Agreement shall be agreed between
the Parties in advance of such announcement. Each Party understands that this
Collaboration Agreement and its efforts hereunder are likely to be of
significant interest to investors, analysts, and others, and each Party
therefore intends to make such public announcements with respect thereto. Each
Party agrees that any such announcement will not contain confidential business
or technical information of the other Party.
ARTICLE 11
TERM AND TERMINATION
11.1 TERM. Unless earlier terminated in accordance with Section 11.2, this
Collaboration Agreement shall expire upon the expiration of the last to expire
Patent Right for which a license is granted hereby.
11.2 TERMINATION FOR MATERIAL BREACH. Each Party shall have the right to
terminate this Collaboration Agreement after 90 days' written notice to the
other that the other is in material breach of this Collaboration Agreement,
unless the other party cures the breach before the expiration of such time
period. Licenses granted to the non-breaching Party under this Collaboration
Agreement shall not be affected by termination for material breach. All licenses
to the breaching Party shall automatically terminate upon such termination.
11.3 SURVIVING OBLIGATIONS. Upon expiration or early termination of this
Collaboration Agreement, the following provisions shall survive, to the extent
applicable: Section 2.5, Articles 8, 9 and 12.
ARTICLE 12
INDEMNIFICATION
12.1 INDEMNIFICATION BY VERSICOR. Versicor hereby indemnifies and holds
harmless Biosearch from and against all Third Party claims, including without
limitation, any claims with respect to death or injury to a person or damage to
property, and all damages, losses, costs and expenses, including reasonable
attorney's fees, which Biosearch may incur arising out of or resulting from (i)
the negligence, recklessness or willful misconduct of Versicor, its Affiliates
or sublicensees or each of their officers, employees or agents in the conduct of
this Agreement, or (ii) the development and commercialization of Hospital
Products in the Versicor Territory. Versicor shall not be obligated to indemnify
Biosearch for any claims, damages, losses, costs or expenses arising out of
Biosearch's negligence, recklessness, or willful misconduct, or that of its
officers, employees or agents.
12.2 INDEMNIFICATION BY BIOSEARCH. Biosearch hereby indemnifies and holds
harmless Versicor from and against all Third Party claims, including without
limitation, any
13.
claims with respect to death or injury to a person or damage to property, and
all damages, losses, costs and expenses, including reasonable attorney's fees,
which Versicor may incur arising out of or resulting from (i) the negligence,
recklessness or willful misconduct of Biosearch, its Affiliates or sublicensees
or each of their officers, employees or agents in the conduct of this Agreement,
or (ii) the development or commercialization of Hospital Products in the
Biosearch Territory. Biosearch shall not be obligated to indemnify Versicor for
any claims, damages, losses, costs or expenses arising out of Versicor's
negligence, recklessness, or willful misconduct, or that of its officers,
employees or agents.
12.3 PROCEDURE. The party seeking indemnification under this Article 12
(the "Indemnified Party") shall (i) give the other party (the "Indemnifying
Party") notice of the relevant claim, (ii) cooperate with the Indemnifying
Party, at the Indemnifying Party's expense, in the defense of such claim, and
(iii) give the Indemnifying Party the right to control the defense and
settlement of such claim, except that the Indemnifying Party shall not enter
into any settlement that affects the Indemnified Party's rights or interest
without the Indemnified Party's prior written approval. The Indemnified Party
shall have no authority to settle any claim on behalf of the Indemnifying Party.
ARTICLE 13
REPRESENTATIONS AND WARRANTIES
13.1 MUTUAL REPRESENTATIONS. Each party hereby represents and warrants:
(a) CORPORATE POWER. Such party is duly organized and validly existing
under the laws of the state of its incorporation and has full corporate power
and authority to enter into this Agreement and has full corporate power and
authority to enter into this Agreement and to carry out the provisions hereof.
(b) DUE AUTHORIZATION. Such party is duly authorized to execute and
deliver this Agreement and to perform its obligations hereunder.
(c) BINDING AGREEMENT. This Agreement is a legal and valid obligation
binding upon it and enforceable in accordance with its terms. The execution,
delivery and performance of this Agreement by such party does not conflict with
any agreement, instrument or understanding, oral or written, to which it is a
party or by which it may be bound, nor violate any law or regulation of any
court, governmental body or administrative or other agency having jurisdiction
over it.
13.2 VERSICOR REPRESENTATIONS. Versicor hereby represents and warrants
that, to the best of its knowledge as of the Collaboration Date, Versicor holds
the right, title and interest in the Versicor Technology sufficient to carry out
its activities under this Agreement, and that use of the Versicor Technology
under this Agreement will not infringe the rights of any Third Party.
13.3 BIOSEARCH REPRESENTATIONS. Biosearch hereby represents and warrants
that, to the best of its knowledge as of the Collaboration Date, Biosearch holds
the right, title and interest
14.
in the Lead Compounds sufficient to carry out its activities under this
Agreement, and that use of the Lead Compounds under this Agreement will not
infringe the rights of any Third Party.
ARTICLE 14
MISCELLANEOUS
14.1 ASSIGNMENT. This Collaboration Agreement may not be assigned or
otherwise transferred by either Party without the consent of the other Party;
provided, however, that either Versicor or Biosearch may, without such consent,
assign its rights and obligations under this Collaboration Agreement in
connection with a merger, consolidation or sale of substantially all of such
Party's assets to an unrelated Third Party.
14.2 GOVERNING LAW. This Agreement shall be governed by and construed in
accordance with the laws of England and Wales notwithstanding the provisions
governing conflict of laws under such law to the contrary, except that matters
of intellectual property law, which shall be determined in accordance with the
intellectual property laws of the jurisdiction relevant to the intellectual
property in question.
14.3 DISPUTE RESOLUTION. In the event of any controversy or claim arising
out of or relating to any provision of this Agreement or the breach thereof, the
parties shall first submit such dispute to the parties' respective executive
officers designated below or their successors, for attempted resolution by good
faith negotiations within fourteen (14) days after such notice is received. Such
designated officers are as follows:
For Versicor: Xxxxxx Xxxxxx, III
Chief Executive Officer
For Biosearch: Francesco Parenti, Ph.D.
President
If such dispute is not resolved between the parties within thirty (30) days
of notice of such dispute as set forth above, either party may commence
international arbitration as provided in this Section 14.3. Such dispute shall
be referred to and finally resolved by arbitration under the London Court of
International Arbitration Rules, which Rules are deemed to be incorporated by
reference into this Section 14.3. The number or arbitrators shall be three, one
of whom shall be a solicitor of at least fifteen (15) years standing. The place
of arbitration shall be London, England. The language to be used in the arbitral
proceedings shall be English.
14.4 RELATIONSHIP OF THE PARTIES. Nothing contained in this Agreement shall
be construed or implied to create an agency, partnership or employer and
employee relationship between Versicor and Biosearch. At no time shall one Party
make commitments or incur any charges or expenses for or in the name of the
other Party.
15.
14.5 FORCE MAJEURE. Neither party shall be held liable or responsible to
the other party nor be deemed to have defaulted under or breached this Agreement
for failure or delay in fulfilling or performing any term of this Agreement when
such failure or delay is caused by or results from causes beyond the reasonable
control of the affected party; including but not limited to fire, floods,
embargoes, war, acts of war (whether war be declared or not), insurrections,
riots, civil commotions, strikes, lockouts or other labor disturbances, acts of
God or acts, omissions or delays in acting by any governmental authority or the
other party; provided, however, it is understood that this Section 14.4(b) is
intended only to suspend and not discharge a party's obligations under this
agreement and that when the causes of the failure or delay are removed or
alleviated, the affected party shall resume performance of its obligations
hereunder.
14.6 NOTICES. Any notice or report required or permitted to be given or
made under this Agreement by one of the parties hereto to the other shall be in
writing, delivered personally or by facsimile (and promptly confirmed by
personal delivery or courier) or courier, postage prepaid, addressed to such
other party at its address indicated below, or to such other address as the
addressee shall have last furnished in writing to the addresser and shall be
effective upon receipt by the addressee.
VERSICOR:
Versicor, Inc.
00000 Xxxxxxxxx Xxxxx
Xxxxxxx, XX 00000
Attention: Xxxxxx X. Xxxxx III
Chief Executive Officer
WITH A COPY TO:
Cooley Godward LLP
Five Palo Alto Square
0000 Xx Xxxxxx
Xxxx Xxxx, XX 00000
Attention: Xxxxxxx X. Xxxxxx, Esq.
BIOSEARCH:
Biosearch Italia, S.P.A.
Xxx X. XxXxxxx 00
00000 Xxxxxxxxx
Xxxxxx, Xxxxx
Attention: Francesco Parenti Ph.D.
President
16.
WITH A COPY TO:
Pavia e Ansaldo
Studio Legale
Xxx xxxxx Xxxxxxxxxx, 0
00000 Xxxxx XXXXX
Attention: Avv X. Xxxxxx De Amicis
Facsimile: x00.0.0000000
14.7 AMENDMENTS. No amendment or modification hereof shall be valid or
binding upon the Parties unless made in writing and signed by both Parties.
14.8 WAIVER. The waiver by either party hereto of any right hereunder or
the failure to perform or of a breach by the other party shall not be deemed a
waiver of any other right hereunder or of any other breach or failure by said
other party whether of a similar nature or otherwise.
14.9 COUNTERPARTS. This 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.
14.10 HEADINGS. The headings of the several sections are inserted for
convenience of reference only and are not intended to be a part of or to affect
the meaning or interpretation of this Agreement.
14.11 LANGUAGE. This Agreement has been prepared in the English language
and, notwithstanding any translations of this Agreement, the English language
shall control its interpretations.
14.12 ENTIRE AGREEMENT. This Agreement contains the entire understanding of
the parties with respect to the subject matter hereof. All express or implied
agreements and understandings, either oral or written, heretofore made are
expressly merged in and made a part of this Agreement.
14.13 SEVERABILITY. Both parties hereby expressly agree and contract that
it is the intention of neither party to violate any public policy, statutory or
common laws, rules, regulations, treaty or decision of any government agency or
executive body thereof of any country or community or association of countries.
Should one or several provisions of the Agreement be or become invalid or
unenforceable by reason of such a violation, then the parties hereto shall
substitute, by mutual consent, valid provisions for such invalid provisions,
which valid provisions in their economic effect come so close to the invalid
provisions that it can be reasonably assumed that the parties would have
contracted this Agreement with those new provisions. In case such provisions
cannot be found, the invalidity of one or several provisions of the Agreement
shall not affect the validity of the Agreement as a whole, unless the invalid
provisions are of such essential importance for this Agreement that it is to be
reasonably
17.
IN WITNESS WHEREOF, the parties have executed this Collaboration Agreement
as of the date first set forth above.
VERSICOR, INC. BIOSEARCH ITALIA, S.P.A.
/s/ XXXXXX X. XXXXXX III /s/ FRANCESCO PARENTI
------------------------------- ---------------------------
Xxxxxx X. Xxxxxx, III Francesco Parenti, Ph.D
Chief Executive Officer President
18.
SCHEDULE 1.3
BIOSEARCH LEAD COMPOUNDS
BIOSEARCH LEAD COMPOUNDS
CLASS OF
PRIORITY NAME OR NUMBER MOLECULE CHEMICAL AMENABILITY BIOLOGICAL PROMISE PROPRIETARY POSITION
---------- ---------------- ------------ ---------------------- -------------------- -----------------------
GE 2270 Thiazole OK Potent gram Strong patent
Peptide positive position
*** MDL 62935 Thiazole OK. Degradation Poor activity as is Strong patent
Peptide product position
MDL 63102 Thiazole OK. Degradation No activity as is Strong patent
Peptide product position
MDL 62766 Teichoplanin Not amenable to Important SAR info Excellent
*** and MDL 62708 aglycone further modification but not intersting for both
derivatives per se
MDL 63995 Teichoplanin Good Gram negative promise Excellent
aglycone also possible VanA
MDL 63879 Fragment of Good Gram negative promise Excellent
aglycone also possible VanA
** L-15722 (actagardine Type C Complex cyclic Narrow Gram None, would require
or Gardimicin) Lantibiotic peptide positive a new derivative
molecule, difficult? but includes VRE
GE 21640 Kirtomycin-like Difficult? Narrow spectrum ???
excluding S.aureus?
GE 71232 Everninomycin-like Difficult Interesting gram Patent pending
positive activity,
nephrotoxic?
** Thermorubin Polyketide Doable but not easy Potent gram None, would require
positive a new derivative
spectrum
* Liplarmycin C-18 Difficult Mediocre gram None, would require
macrolide positive a new
no in vivo activity derivative
Purpuromycin Polyketide OK,potential Gram positive & None, would require
scaffold? negative a new derivative
and fungii
Azalomycin polyene very difficult Narrow spectrum Excellent
macrolide antifungal activity
** MDL 63572 Cyclic Fair Enyme inhibitor, no Patent to be filed
peptide activity on whole
cells
PRIORITY NAME OR NUMBER MECHANISM OF ACTION COMMENTS
---------- ---------------- --------------------- -----------
GE 2270 Protein synthesis-EFTu Parent molecule
*** MDL 62935 Protein synthesis-EFTu Good starting point
MDL 63102 Protein synthesis? Novel generic building block or
starting point for EFTu inhib's
MDL 62766 binding to cell wall These are semi synthetic analogues
*** and MDL 62708 substrate that will not be further developed
MDL 63995 binding to cell wall Excellent starting point for
substrate glycopeptide with novel activity
MDL 63879 binding to cell wall More distant starting point for
substrate same type of modifications
** L-15722 (actagardine transglycosylase Several other related
or Gardimicin) inhibitor molecules
cell wall synthesis described in the literature
GE 21640 Protein synthesis-EFTu Could make elfamycin analogues
GE 71232 Not certain possibly Scheering Plough has an anologue
protein synthesis in phase 1,major formulation issue
** Thermorubin Protein synthesis Major serum inactivation problem
* Liplarmycin RNA polymerase Two other related families known
Purpuromycin Protein synthesis Serum inactivation problem
toxicity likely to be an issue
Azalomycin Membrane active Development candidate as topical?
** MDL 63572 RNA polymerase Modulators effort might help
inhibitor guide synthetic effort
*** Of immediate interest
** 2nd tier interest
* Possible interest
Page 1
SCHEDULE 2.1
COMPOUND DEVELOPMENT PLAN
[Initial Outline]
COMPOUND DEVELOPMENT PLAN
===============================================================================
BIOSEARCH PROVIDES TO
VERSICOR LIST OF POTENTIAL
LEADS FOR OPTIMISATION
VERSICOR SELECTS SPECIFIC
LEADS BASED ON CHEMICAL
AND BIOLOGICAL SUITABILITY
BIOSEARCH PROVIDES VERSICOR
WITH STARTING MATERIAL
VERSICOR CONDUCTS PRELIMINARY 6 MONTH
CHEMISTRY PROGRAM TO ASSESS PRACTICABILITY
VERSICOR INFORMS JLDC OF DECISION TO INITIATE
FULL BLOWN MODIFICATION PLAN TO SYNTHESIZE
IMPROVED ANALOGUES FOR UP TO 18 MONTHS
FURTHER
IMPROVEMENT
ANALOGUES EVALUATED IN VITRO
BY VERSICOR FOR POTENCY SPECTRUM
AND OTHER RELEVANT PROPERTIES
FURTHER
IMPROVEMENT
DECISION BY JMC TO ADVANCE IMPROVED ANALOGUE
TO BIOSEARCH FOR IN VIVO STUDIES ON EFFICACY
PK AND GROSS TOXICTY
OPTIMISED LEAD FURTHER CHARECTERISED AND SELECTED FOR
INTERNAL DEVELOPMENT OR OUTLICENSING BY JMC
