EXHIBIT 10.9
CONFIDENTIAL TREATMENT REQUESTED
AGREEMENT
This Agreement is entered into as of January 31, 1989 ("Effective
Date"), by and between X. XXXXXXXX-XX XXXXX & CO. LIMITED COMPANY of Basle,
Switzerland ("X. Xxxxx) and PROTEIN DESIGN LABS, INC., a Delaware corporation
having offices at 0000 Xxxxxx Xxxxx, Xxxx Xxxx, Xxxxxxxxxx 00000 ("PDL").
WITNESSETH
WHEREAS, PDL has developed a body of technology relating to humanizing
antibodies and, in particular, to humanized antibodies against the
interleukin-2 receptor ("IL-2R");
WHEREAS, PDL and Xxxxxxxx-Xx Xxxxx Inc. ("Roche"), a New Jersey
corporation, are contemporaneously entering into an agreement ("PDL/Roche
Agreement") which will govern a scientific collaboration, clinical development
program and subsequent commercialization in the Roche Territory (as defined in
Section 1.13 hereof) of pharmaceutical products based on PDL's proprietary
technology relating to such humanized antibodies;
WHEREAS, X. Xxxxx has proven experience in the development, clinical
research, registration, manufacturing and marketing of pharmaceutical
products;
WHEREAS, PDL and X. Xxxxx desire X. Xxxxx to register and market such
pharmaceutical products in countries of the world outside the Roche Territory,
and now wish to embody their mutual understandings in a full text, binding
agreement;
NOW THEREFORE, in consideration of the premises and the mutual promises
and covenants set forth below, PDL and X. Xxxxx mutually agree as follows:
I. DEFINITIONS
For the purposes of this Agreement, the following terms, when written
with an initial capital letter, shall have the meaning ascribed to them below.
1.01 "Affiliate" means any corporation or other business entity
controlled by, controlling, or under common control with a party to this
Agreement through common share holdings, with "control" meaning direct or
indirect beneficial ownership of more than fifty percent (50%) of the voting
stock of, or more than a fifty percent (50%) interest in the income of, such
corporation or other business entity; and any corporation in which the maximum
amount of stock permitted by law to be held by another entity is beneficially
owned, directly or indirectly, by X. Xxxxx.
1.02 "Combination Product" means any product containing both an
ingredient which causes it to be considered a Licensed Product and one or more
other therapeutically active ingredients.
1.03 "Field" means any humanized or chimeric antibody which binds to
the IL-2R, where "humanized" means a genetically engineered combination of a
substantially human framework region and constant region, and complementarity
determining regions from non-human antibodies, and where "chimeric" means a
genetically engineered combination of a human constant region and non-human
variable region. "Antibodies in the Field" means humanized and chimeric
antibodies which bind to the IL-2R. It is believed that these Antibodies in
the Field may be useful for therapeutic, diagnostic, imaging and similar
purposes. It is understood that the Field includes, but is not limited to,
that certain humanized murine monoclonal antibody prepared against the p55
component of the IL-2R ("humanized anti-Tac"). Furthermore, the Field
includes, but is not limited to, all improvements relating to humanized anti-
Tac including without limitation modifications in structure introduced by
genetic engineering, or by chemical or enzymatic cleavage. Also included
within the Field shall be alternate hosts for producing humanized anti-Tac,
methods for purification, formulations incorporating humanized anti-Tac, and
uses and methods of use for humanized anti-Tac in human medicine.
1.04 "Initial Commercialization" means the end of the calendar month
containing the date following the granting of Regulatory Approval (as defined
in Section 1.10 hereof) for a Licensed Product for human therapeutic use for
prevention of kidney transplant rejection or a major disease (within the
meaning of Milestone #2 in Section 3.02 of the PDL/Roche Agreement) on which
X. Xxxxx, its Affiliates or sublicensees first sell such a product to an
independent third party not an Affiliate of the seller in a major market
within the Territory, where "major market" means either Japan or two of the
following three countries: France, Italy or the United Kingdom.
1.05 "Joint Inventions" means any inventions in the Field, whether
patented or not, which are jointly made during the period beginning on the
Effective Date and ending one year after termination of the Research Program
(as defined in Section 1.11 hereof) by at least one PDL employee or person
contractually required to assign or license patent rights covering such
inventions to PDL and at least one X. Xxxxx or Roche employee or person
contractually required to assign or license patent rights covering such
inventions to X. Xxxxx or Xxxxx.
1.06 "Licensed Product" means any product in the Field, including any
Combination Product, the making, use or sale of which utilizes PDL Know-How,
PDL Patents or Joint Inventions or would, in the absence of this Agreement,
infringe a Valid Claim.
1.07 "Net Sales" means the gross invoice price ("GIP") of all Licensed
Products sold or otherwise disposed of for consideration by X. Xxxxx, its
Affiliates or sublicensees to independent third parties not an Affiliate of
the seller, as computed in the central X. Xxxxx Swiss Francs Sales Statistics
for the countries concerned, whereby the amount of such sales in foreign
currencies is converted into Swiss Francs at the average monthly rate of
exchange at the time, after deducting, if not already deducted, from the
amount invoiced:
(a) the amounts actually allowed as volume or quantity
discounts, sales rebates (including cash discounts), price reductions, returns
(including withdrawals and recalls); and
(b) sales, excise and turnover taxes imposed directly upon and
actually paid by X. Xxxxx, its Affiliates or sublicensees.
In addition, there shall be deducted, to the extent not already deducted
from the amount invoiced, an amount equal to seven percent (7%) of the GIP to
cover all other expenses or discounts, including but not limited to customs
duties, transportation and insurance charges and other direct expenses.
In the case of Combination Products for which the Licensed Product and
each of the other therapeutically active ingredients contained in the
Combination Product have established market prices when sold separately, Net
Sales shall be determined by multiplying the Net Sales for each such
Combination Product by a fraction, the numerator of which shall be the
established market price for the Licensed Product(s) contained in the
Combination Product, and the denominator of which shall be sum of established
market prices for the Licensed Product(s) plus the other active ingredients
contained in the Combination Product. When such separate market prices are
not established, then the parties shall negotiate in good faith to determine
the method of calculating Net Sales for Combination Products.
If X. Xxxxx or its Affiliates or sublicensees receive non-cash
consideration for any Licensed Product sold or otherwise transferred to an
independent third party not an Affiliate of the seller or transferor, the fair
market value of such non-cash consideration on the date of the transfer as
known to X. Xxxxx, or as reasonably estimated by X. Xxxxx if unknown, shall be
included in the definition of Net Sales.
1.08 "PDL Know-How" means, except as otherwise set forth in this
Section 1.08, all inventions, discoveries, trade secrets, information,
experience, data, formulas, procedures and results in the Field, and
improvements thereon, including any information regarding the structure,
sequence and characterization of Antibodies in the Field, methods of making
and the characterization of cell lines producing Antibodies in the Field, and
methods of achieving high levels of expression of Antibodies in the Field,
which are rightfully held by PDL as of the Effective Date, or which are
developed or acquired by PDL during the period beginning on the Effective Date
and ending one year after termination of the Research Program, and which Know-
How is needed for registration, manufacturing, using or selling products in
the Field; provided, however, that PDL Know-How excludes any Know-How of any
kind concerning generic methods of designing, developing or preparing
antibodies including, but not limited to, methods of humanizing antibodies,
methods of reducing the immunogenicity of antibodies, and methods of
increasing the affinity of antibodies.
1.09 "PDL Patents" means all patent applications owned or controlled by
PDL ("Sole PDL Patents") and all patent applications resulting from Joint
Inventions ("Joint Roche-PDL Patents") containing claims in the Field, which
are filed prior to or during the term of this Agreement in the United States
or any foreign jurisdiction, including any addition, continuation,
continuation-in-part or division thereof or any substitute application
therefor; any patent issued with respect to such patent application, any
reissue, extension or patent term extension of any such patent, and any
confirmation patent or registration patent or patent of addition based on any
such patent; and any other United States and foreign patent or inventor's
certificate covering claims in the Field.
1.10 "Regulatory Approval" means the granting of all governmental
regulatory approvals required, if any, for the sale of a Licensed Product in a
given country or jurisdiction within the Territory.
1.11 "Research Program" means the collaborative scientific research
program between PDL and Roche described more fully in Article VI of the
PDL/Roche Agreement.
1.12 "X. Xxxxx Inventions" means any inventions in the Field which are
made during the term of this Agreement by employees of X. Xxxxx or persons
contractually required to assign or license patent rights covering such
inventions to X. Xxxxx.
1.13 "Roche Territory" means the United States of America and its
territories and possessions where the patent laws of the United States are in
force. It is understood that the PDL/Roche Agreement comprises a separate but
complementary license agreement covering activities in the Roche Territory.
1.14 "Territory" means all countries of the world excluding the Roche
Territory.
1.15 "Valid Claim" means a claim in any issued patent within the PDL
Patents which has not been disclaimed or held unenforceable or invalid by a
decision of a court or governmental agency of competent jurisdiction by a
decision beyond right of review.
II. LICENSE GRANT
2.01 License Grant. PDL grants to X. Xxxxx and to X. Xxxxx'x
Affiliates the sole and exclusive right to the PDL Know-How and the PDL
Patents, but only to the extent necessary to make, have made, use and sell
Licensed Products in the Field within the Territory. For so long as X. Xxxxx
is in compliance with its obligations under Section 5.01 hereof, X. Xxxxx may
sublicense the right to make, have made, use and sell Licensed Products in the
Field within the Territory, but no other rights may be sublicensed. Any such
sublicense shall be subject to Section 3.05 hereof, and shall terminate
automatically if X. Xxxxx or Xxxxx shall not have remedied or initiated steps
to remedy a breach of Section 5.01 hereof or Section 7.01 of the PDL/Roche
Agreement, respectively, in a manner reasonably satisfactory to PDL within
sixty (60) days after receipt by X. Xxxxx of notice of such breach from PDL.
2.02 Identification of Patents. Set forth on Appendix A is a list
identifying patents or patent applications which comprise Sole PDL Patents.
PDL shall update this list by delivering a supplement to X. Xxxxx no less
frequently than once per year during the term of this Agreement.
CONFIDENTIAL TREATMENT REQUESTED
III. ROYALTIES
3.01 X. Xxxxx agrees to pay PDL royalties for sales of Licensed
Products and Combination Products according to the schedule and terms set
forth below:
(a) Years 1 through 3. Prior to and for the first three (3)
years following Initial Commercialization of a particular Licensed Product,
X. Xxxxx shall pay PDL royalties on sales of that product at a rate determined
by the aggregate annual worldwide Net Sales of all Licensed Products as
follows:
Net Sales ($ in millions) Royalty Rate
Up to and including [ ] [ ]
Amount in excess of [ ] but not exceeding [ ] [ ]
Over [ ] [ ]
For purposes of computing aggregate annual worldwide Net Sales,
X. Xxxxx'x Net Sales in the Territory will be combined with the Net Sales of
Roche within the Roche Territory. This same understanding is being
incorporated into the PDL/Roche Agreement.
(b) Years 4 and Succeeding. For the fourth and each succeeding
year following Initial Commercialization, X. Xxxxx shall pay PDL royalties in
accordance with the provisions of Section 3.01(a) for Net Sales in a
particular country, provided either (i) the Licensed Product or its method of
manufacture (wherever actually manufactured) is covered by a Valid Claim in
the country of sale, or (ii) the Licensed Product is manufactured in a country
where the method of manufacture is covered by a Valid Claim (together, (i) and
(ii) are referred to as the "Patentability Criteria").
Subject to Section 3.02 below, if neither of the Patentability Criteria
have been satisfied, then Roche shall pay PDL a royalty rate of [
] of the Net Sales in the country of sale for the duration of this
Agreement or until such time as one of the Patentability Criteria is
satisfied, at which time X. Xxxxx shall resume paying PDL royalties at the
rates specified in Section 3.01(a) above.
(c) Expiration. X. Xxxxx'x obligation to pay royalties to PDL
hereunder shall expire with respect to sales in any particular country of any
particular Licensed Product on the later of the expiration of all Valid
Claims covering such Licensed Product or the [ ] anniversary of
Initial Commercialization of such Licensed Product in the Territory.
(d) Antibodies in the Field Not Provided or Developed by PDL.
In consideration of the disclosure to X. Xxxxx of PDL Know-How and cell lines
as provided for herein, X. Xxxxx agrees that products incorporating or using
antibodies in the Field which are not provided or developed by PDL shall
nevertheless be presumed to utilize PDL Know-How, with such presumption being
rebuttable by clear and convincing evidence with respect to sales of such
products made in those countries listed on Appendix B, and such presumption
being conclusive as between the parties hereto with respect to sales of such
products made anywhere else within the Territory. Accordingly, X. Xxxxx shall
pay PDL royalties on sales of each such product in the Territory (except for
sales with respect to which the above rebuttable presumption has in fact been
refuted by Roche) for a period of [ ] years from Initial
Commercialization of such product in accordance with the terms of this
Section 3.01, and such sales shall constitute "Net Sales" for purposes hereof.
3.02 De Facto Exclusivity. For purposes of this Article III, the term
"de facto exclusivity" means that X. Xxxxx, together with its Affiliates and
sublicensees, controls at least [ ] of the market for a particular
Licensed Product in a country as measured by unit sales. If neither of the
Patentability Criteria have been satisfied and X. Xxxxx does not enjoy de
facto exclusivity for a particular Licensed Product in a particular country at
any time after [ ] years following Initial Commercialization of such
Licensed Product, then X. Xxxxx shall pay PDL a royalty rate of [ ] of
the Net Sales of such Licensed Product in the country of sale until the [
] anniversary of Initial Commercialization, or until X. Xxxxx shall
acquire de facto exclusivity for that product or until such time as either of
the Patentability Criteria is satisfied (at which time X. Xxxxx shall resume
paying PDL royalties at the rates specified in Sections 3.01(a) or (b) above,
whichever is applicable). Valid Claims and de facto exclusivity are to be
determined on a country-by-country basis.
3.03 Foreign Filing Expenses Credited Against Royalties. X. Xxxxx
shall have the right to credit [ ] of all Foreign Filing Expenses (as
defined in Section 5.02 below) actually paid to PDL against future royalties
due to PDL pursuant to this Article III provided that such credits, when added
to the offset provided for in Section 3.04 below, may not reduce the royalties
to be paid to PDL to less than [ ] of the amount which would
otherwise be due pursuant to Section 3.01 hereof.
3.04 Offset for Third Party Licenses.
(a) If PDL and X. Xxxxx agree in writing that either party must
obtain a license from an independent third party in order for X. Xxxxx to
manufacture, use or sell a Licensed Product in the Territory and if PDL and
X. Xxxxx agree upon the terms of such license ("Third Party License"), then
the parties shall [ ] the cost of that license [ ].
Such cost includes license fees and any other fixed costs associated with the
Third Party License as well as any royalties. The parties then shall, within
thirty (30) days, reimburse each other in the manner necessary to effect a [
] of such license fees and other fixed costs.
(b) PDL's share of the royalties portion of the cost of any
Third Party License, shall be (i) accrued against and deducted from any
royalties due to PDL from X. Xxxxx pursuant to Sections 3.01 and 3.02 if
X. Xxxxx pays the royalties due under the Third Party License to such third
party, and (ii) accrued in favor of and added to any royalties due to PDL from
X. Xxxxx pursuant to Sections 3.01 and 3.02 if PDL pays the royalties due
under the Third Party License to such third party; provided, however, that
this addition or offset shall not cause PDL's royalties to be reduced under
the schedule set forth in Section 3.01 to less than [ ] of Net
Sales in any year, or under Sections 3.01(b) and 3.02 to less than [
] if X. Xxxxx has de facto exclusivity and [ ] if
X. Xxxxx does not have de facto exclusivity, and provided further, that
X. Xxxxx'x total royalty obligations to PDL under Sections 3.01 and 3.02 when
added to those royalties payable to third parties pursuant to Third Party
Licenses shall not exceed [ ] of Net Sales in any year.
3.05 Sublicenses. Any Net Sales of an X. Xxxxx sublicensee shall be
treated as Net Sales of X. Xxxxx for purposes of royalty payments hereunder.
If X. Xxxxx shall grant any sublicenses under this Agreement, then X. Xxxxx
shall obtain the written commitment of such sublicensees to abide by all
applicable terms and conditions of this Agreement and X. Xxxxx shall remain
responsible to PDL for the performance of any and all terms by such
sublicensee. All such sublicenses shall terminate on termination of this
Agreement.
3.06 Royalties upon Termination. If this Agreement is terminated
pursuant to Sections 7.02, 7.03 or 7.04 below, X. Xxxxx shall continue to pay
PDL any royalties earned pursuant to this Article III prior to the date of
termination and any royalties earned thereafter as a result of sales under
Section 7.05.
IV. ACCOUNTING AND PAYMENTS
4.01 Semi-Annual Royalty Payments and Reports. X. Xxxxx agrees to make
royalty payments and written reports to PDL following the end of every
calendar half-year covering all sales of Licensed Products by X. Xxxxx, its
Affiliates or sublicensees for which invoices were sent during such half-year
period. X. Xxxxx shall exercise its best efforts to render such reports
within forty-five (45) days after the end of each calendar half-year period,
but in no event shall such reports be rendered by X. Xxxxx later than
sixty (60) days after the end of each calendar half-year period. Each report
shall state:
(a) for Licensed Products disposed of by sale, the quantity,
description, country(ies) of manufacture and sale, Net Sales, GIP and the
deductions pursuant to Section 1.07 by which such GIP is reduced to Net Sales,
(b) for Licensed Products disposed of other than by sale, the
quantity, description, country(ies) of manufacture and disposition, and nature
of the disposition, and
(c) the calculation of royalties due to PDL for such period
pursuant to Section 1.07 and Article III hereof.
The information contained in each such report shall be considered
confidential and PDL agrees not to disclose such information to any third
party except as may be required by law, or to PDL's shareholders during such
time as PDL is a privately-held company pursuant to any contract among PDL and
such shareholders. Each report shall reconcile aggregate annual Net Sales
attributable to X. Xxxxx with aggregate annual worldwide Net Sales
attributable to Roche. Concurrent with the making of each report, X. Xxxxx
shall include payment due PDL of royalties for the period covered by such
report.
It is understood that pursuant to this provision, only one royalty shall
be payable on a given unit of Licensed Product disposed of under this
Agreement. In the case of transfers or sales of any Licensed Product between
Roche, X. Xxxxx or an Affiliate or sublicensee of Roche or X. Xxxxx, only one
royalty payment shall be due, and such royalty shall be payable with respect
to the sale of such Licensed Product to an independent third party not an
Affiliate of the seller.
4.02 Termination Report. X. Xxxxx also agrees to make a written report
to PDL within ninety (90) days after the date on which X. Xxxxx, Xxxxx or
their Affiliates or sublicensees last sell a Licensed Product, stating in such
report the same information called for in each semi-annual report by
Section 4.01 for all Licensed Products and Combination Products made, sold or
otherwise disposed of and upon which were not previously reported to PDL.
4.03 Accounting. X. Xxxxx agrees to keep full, clear and accurate
records for a period of at least three (3) years, or such longer period as may
coincide with X. Xxxxx'x internal records retention policy, setting forth the
manufacturing, sales and other disposition of Licensed Products and
Combination Products sold or otherwise disposed of under the license herein
granted in sufficient detail to enable royalties payable to PDL hereunder to
be determined. X. Xxxxx further agrees to permit its books and records to be
examined by an independent accounting firm selected by PDL from time to time
to the extent necessary to verify reports provided for in Sections 4.01 and
4.02 above. Unless PDL obtains the prior written consent of X. Xxxxx, such
accounting firm must be a foreign representative of one of those firms
commonly referred to in the United Sates as the "Big Eight" firms. Such
examination is to be made at the expense of PDL, except in the event that the
results of the audit reveal a discrepancy in favor of X. Xxxxx of 10% or more
over the period being audited, in which case reasonable audit fees for such
examination shall be paid by X. Xxxxx.
4.04 Methods of Payment. All payments due to PDL hereunder shall be
paid in United States dollars by wire transfer to a bank in the United States
designated in writing by PDL. Conversion from Swiss Francs into the
equivalent in United States dollars shall be made at the rate of exchange for
buying funds as quoted and confirmed by the Swiss Bank Corporation in Basle,
Switzerland for the last business day of each calendar half-year.
4.05 Withholding Taxes. If law or regulation requires the withholding
of any taxes due by X. Xxxxx'x Affiliates or sublicensees on Net Sales by such
Affiliates or sublicensees in a given country in the Territory, the parties
shall confer regarding possible alternative arrangements to lawfully avoid
such withholding. If, between a country in the Territory and any other place
as designated, a treaty for the avoidance of double taxation is in force and
such treaty reduces or eliminates the withholding of any taxes otherwise due
on royalties payable from such country, PDL may (but shall not be obligated
to) request a direct remittance of royalties to PDL at such place that PDL may
designate hereunder. If the parties are unable to formulate or agree upon
action to lawfully avoid withholding, then the parties agree that fifty
percent (50%) of such taxes shall be applied to reduce the Net Sales amount
for sales of Licensed Products in such country. Notwithstanding the
foregoing, X. Xxxxx shall be solely responsible for any withholding of taxes
due on royalties payable from Japan and the countries listed on Appendix B.
4.06 Currency Transfer Restrictions. If in any country in the
Territory the payment or transfer of royalties on Net Sales in such country is
prohibited by law or regulation, the parties hereto shall confer regarding the
terms and conditions on which Licensed Products shall be sold in such
countries, including the possibility of payment of royalties to PDL in local
currency to a bank account in such country or the re-negotiation of royalty
rates and terms for such sales. However, PDL shall be under no obligation to
accept terms and conditions other than those set forth herein, and if the
parties do not reach an alternative agreement then X. Xxxxx shall either
(a) remain responsible for royalties payable to PDL with respect to Net Sales
in such countries, or (b) cease sales in such countries, which shall not be
deemed a breach by X. Xxxxx of its due diligence obligations under
Section 5.01 below.
V. CERTAIN COVENANTS OF X. XXXXX
5.01 Diligence. X. Xxxxx shall use reasonable diligence in proceeding
with registering, marketing and selling Licensed Products within the Territory
in the event such products are developed as a result of the PDL/Roche
Agreement. Reasonable diligence as used in this Agreement shall mean the same
standard of effort used by X. Xxxxx in registering, marketing and selling its
own protein-based products which must receive Regulatory Approval. The
parties acknowledge that X. Xxxxx does not register, market and sell its own
protein-based products in every country within the Territory, and it is
understood that the exercise by X. Xxxxx of reasonable diligence is to be
determined by judging its efforts in the Territory taken as a whole. If
X. Xxxxx fails to exercise such diligence, PDL may terminate this Agreement
and X. Xxxxx'x rights hereunder pursuant to Section 7.04 below.
5.02 Reimbursement for Costs of Patent Applications.
(a) X. Xxxxx agrees to reimburse PDL for all ex parte out-of-
pocket expenses incurred by PDL after the Effective Date hereof in connection
with the prosecution and maintenance in the Territory of patent applications
and patents included within the Sole PDL Patents or Joint Roche-PDL Patents
for which PDL makes filings pursuant to Article IX of the PDL/Roche Agreement
("Foreign Filing Expenses"). X. Xxxxx shall make such payments to PDL no
less frequently than semi-annually, within thirty (30) days after submission
by PDL of a reasonably itemized statement of such expenses incurred
by PDL during the relevant six-month period. Notwithstanding the
foregoing, X. Xxxxx shall not be obligated to reimburse PDL for such expenses
exceeding an aggregate of [ ] in any calendar year.
(b) Prior to the filing of a patent application in the
Territory, PDL shall inform X. Xxxxx concerning such proposed filing and shall
consult with X. Xxxxx concerning the proposed filing procedures, including
specifically the determination of the scope of any such patent and the
countries in which such application is to be filed. PDL shall regularly
advise X. Xxxxx of any substantial action or development in the prosecution of
its patent applications and patents in the Territory, in particular of the
question of scope of, the issuance of, the rejection of, or an opposition to
any respective patent application or patent.
(c) X. Xxxxx shall be entitled to a credit against royalties
payable hereunder as provided in Section 3.03 hereof.
VI. OWNERSHIP OF TECHNOLOGY
6.01 PDL Technology. Ownership of the PDL Know-How and Sole PDL
Patents shall remain vested at all times in PDL. Notwithstanding the
provisions of Section 2.01, PDL expressly reserves under this Agreement
(i) all rights to use the PDL Know-How and Sole PDL Patents to make, have
made, use and sell anywhere in the world all products not within the Field and
(ii) the right to use the PDL Know-How and Sole PDL Patents for PDL's internal
research purposes in the Field.
6.02 Joint Inventions and Joint Roche-PDL Patents. Ownership of Joint
Inventions and Joint Roche-PDL Patents shall be vested jointly in PDL and
Roche. X. Xxxxx shall have the exclusive right to make, have made, use or
sell any Joint Invention or Joint Roche-PDL Patent in the Field within the
Territory during the term of the Agreement. Both parties shall have the non-
exclusive right to make, have made, use or sell any Joint Invention or Joint
Roche-PDL Patent outside the Field during the term of the Agreement, and
neither party shall be obligated to account to the other for such use. Upon
the expiration or termination of the Agreement, both parties shall have the
non-exclusive right to make, have made, use or sell any Joint Invention or
Joint Roche-PDL Patent without restriction and without any obligation to
account to the other party for such use. Notwithstanding the foregoing or the
provisions of Section 2.01, PDL expressly reserves the right to use Joint
Inventions and Joint Roche-PDL Patents for PDL's internal research purposes in
the Field and to carry out its obligations under the PDL/Roche Agreement.
6.03 X. Xxxxx Inventions. PDL hereby acknowledges that this Agreement
does not grant PDL any ownership rights in the X. Xxxxx Inventions.
VII. TERM AND TERMINATION
7.01 Term. Unless earlier terminated pursuant to the terms of this
Article VII, this Agreement shall remain in effect until the later of (a) the
date of expiration of the last to expire of any Valid Claims in any country or
(b) the date of the [ ] anniversary of Initial Commercialization of
the last Licensed Product to be introduced by X. Xxxxx hereunder, at which
time this Agreement shall automatically expire.
7.02 Termination by Mutual Agreement. This Agreement may be terminated
by the written agreement of the parties.
7.03 Termination by X. Xxxxx. X. Xxxxx may terminate this Agreement
upon ninety (90) days written notice to PDL.
7.04 Termination by Default. If either party defaults in the
performance of, or fails to be in compliance with, any material agreement,
condition or covenant of this Agreement, the party not in default may
terminate this Agreement at its option; provided, however, that if such event
of default or non-compliance is the first occurrence of an event giving rise
to the right of termination pursuant to this Section 7.04, the non-defaulting
party may terminate this Agreement only if such default or noncompliance shall
not have been remedied, or steps initiated to remedy the same to the other
party's reasonable satisfaction within sixty (60) days after receipt by the
defaulting party of a written notice thereof from the other party. If PDL
terminates the PDL/Roche Agreement pursuant to Section 11.04 thereof, PDL may
elect to simultaneously terminate this Agreement upon written notice to
X. Xxxxx. If Xxxxx terminates the PDL/Roche Agreement pursuant to
Section 11.04 thereof, X. Xxxxx may elect to simultaneously terminate this
Agreement upon written notice to PDL.
7.05 Inventory. Upon termination of this Agreement, PDL hereby grants
X. Xxxxx a license to sell within one (1) year of such termination any
Licensed Products in X. Xxxxx'x or its Affiliates or sublicensee's inventory
on the date of such termination, which have not previously been sold
("Inventory"); provided, however that X. Xxxxx shall pay the royalties due on
such Inventory in the amounts and manner provided for in Articles III and IV.
7.06 Return of Materials. Subject to Section 7.08 hereof concerning
archival copies, upon termination of this Agreement by X. Xxxxx pursuant to
Section 7.03 or by either or both parties pursuant to Sections 7.02 or 7.04,
X. Xxxxx forthwith shall return to PDL all cell lines and their progeny,
antibodies and other biological materials provided by PDL under the PDL/Roche
Agreement.
7.07 Rights and Obligations on Termination or Expiration. Unless
expressly provided to the contrary, the provisions of Sections 3.06 and 5.03
and Articles IV, VIII, IX and XI shall survive the termination of this
Agreement. Upon the expiration of this Agreement pursuant to
Section 7.01 above, if it is not otherwise terminated pursuant to this Article
VII, PDL shall grant to X. Xxxxx a [ ] license to use
the PDL Know-How and Sole PDL Patents and cell lines delivered by
PDL pursuant to the PDL/Roche Agreement, but only to the extent necessary
to make, have made, use and sell Licensed Products in the Field within
the Territory.
7.08 Archival Copies. Section 7.06 notwithstanding, each party shall
be entitled to keep for archival purposes one copy of all written materials
returned to the other party pursuant to Section 7.06.
VIII. CONFIDENTIALITY, DISCLOSURE AND PUBLICATIONS
8.01 Confidentiality. During the term of this Agreement and for a
period of five (5) years following expiration or termination of this
Agreement, each party shall maintain in confidence all information and
materials including, but not limited to, cell lines, their progeny, and
antibodies, disclosed by the other party hereto which such party knows or has
reason to know are or contain trade secrets or other proprietary information
of the other, including, without limitation, information relating to the PDL
Know-How, PDL Patents, Joint Inventions and inventions of the other party, and
the business plans of the other party, including, without limitation,
information provided by either party to the other party hereto prior to the
Effective Date, and shall not use such trade secrets or proprietary
information for any purpose, including, without limitation, for the purpose of
developing products in the Field except as permitted by this Agreement or
disclose the same to anyone other than those of its Affiliates, sublicensees,
employees, consultants, agents or subcontractors as are necessary in
connection with such party's activities as contemplated in this Agreement.
Each party shall be responsible for ensuring compliance with these obligations
by such party's Affiliates, sublicensees, employees, consultants, agents and
subcontractors. Each party shall use a similar effort to that which it uses
to protect its own most valuable trade secrets or proprietary information to
ensure that its Affiliates, sublicensees, employees, consultants, agents and
subcontractors do not disclose or make any unauthorized use of trade secrets
or proprietary information of the other party hereto. Each party shall notify
the other promptly upon discovery of any unauthorized use or disclosure of the
other's trade secrets or proprietary information.
8.02 Exceptions. The obligation of confidentiality contained in this
Agreement shall not apply to the extent that (a) either party (the
"Recipient") is required to disclose information by order or regulation of a
governmental agency or a court of competent jurisdiction or (b) the Recipient
can demonstrate that (i) the disclosed information was at the time of such
disclosure by the Recipient already in the public domain other than as a
result of actions of the Recipient, its Affiliates, employees, licensees,
agents or subcontractors, in violation hereof; (ii) the disclosed information
was rightfully known by the Recipient or its Affiliates (as shown by its
written records) prior to the date of disclosure to the Recipient in
connection with the negotiation, execution or performance of this Agreement;
or (iii) the disclosed information was received by the Recipient or its
Affiliates on an unrestricted basis from a source unrelated to any party to
this Agreement and not under a duty of confidentiality to the other party, or
(c) the Recipient can demonstrate that disclosure to a regulatory authority is
required by its product license approval process.
IX. DISPUTE RESOLUTION
9.01 Arbitration. Any claim, dispute or controversy arising out of or
in connection with or relating to this agreement or the breach or alleged
breach thereof shall be submitted by the parties to arbitration by the
American Arbitration Association in Santa Xxxxx County, California under the
commercial rules then in effect for that Association except as provided
herein. All proceedings shall be held in English and a transcribed record
prepared in English. The parties shall choose, by mutual agreement, one
arbitrator within thirty (30) days of receipt of notice of the intent to
arbitrate. If no arbitrator is appointed within the times herein provided or
any extension of time which is mutually agreed upon, the Association shall
make such appointment within thirty (30) days of such failure. The award
rendered by the arbitrator shall include costs of arbitration, reasonable
attorneys' fees and reasonable costs for expert and other witnesses, and
judgment on such award may be entered in any court having jurisdiction
thereof. The parties shall be entitled to discovery as provided in
Sections 1283.05 and 1283.1 of the Code of Civil Procedure of the State of
California, whether or not the California Arbitration Act is deemed to apply
to said arbitration. Nothing in this Agreement shall be deemed as preventing
either party from seeking injunctive relief (or any other provisional remedy)
from any court having jurisdiction over the parties and the subject matter of
the dispute as necessary to protect either party's name, proprietary
information, trade secrets, know-how or any other proprietary right. If the
issues in dispute involve scientific or technical matters, any arbitrator
chosen hereunder shall have educational training and/or experience sufficient
to demonstrate a reasonable level of knowledge in the field of biotechnology.
Judgment upon the award rendered by the arbitrator may be entered in any court
having jurisdiction thereof.
X. FORCE MAJEURE
10.01 If either party shall be delayed, interrupted in or prevented from
the performance of any obligation hereunder by reason of force majeure
including an act of God, fire, flood, earthquake, war (declared or
undeclared), public disaster, strike or labor differences, governmental
enactment, rule or regulation, or any other cause beyond such party's control,
such party shall not be liable to the other therefor; and the time for
performance of such obligation shall be extended for a period equal to the
duration of the contingency which occasioned the delay, interruption or
prevention. The party invoking such force majeure rights of this subparagraph
must notify the other party by registered letter within a period of
fifteen (15) days, from the first and last day of the force majeure unless the
force majeure renders such notification impossible in which case notification
will be made as soon as possible. If the delay resulting from the force
majeure exceeds six (6) months, both parties shall consult together to find an
appropriate solution.
XI. MISCELLANEOUS
11.01 Representations of PDL. PDL represents and warrants to X. Xxxxx
that, except as may otherwise be disclosed in writing to X. Xxxxx:
(a) PDL has the full right and authority to enter into this
Agreement;
(b) to the best knowledge of PDL after reasonable investigation,
no third party has any right, title or interest in the Sole PDL Patents or PDL
Know-How as the result of such third party's former employment of any PDL
employee;
(c) PDL is not aware of any patent or other proprietary rights
of third parties which might be infringed by the Sole PDL Patents or the PDL
Know-How.
11.02 Assignment. This agreement and the licenses herein granted other
than the PDL/Roche Agreement relating to the same Field but for the Roche
Territory shall be binding upon and shall inure to the benefit of, successors
of the parties hereto, or to an assignee of all of the good will and entire
business and assets of a party hereto relating to pharmaceutical and
veterinary products but shall not otherwise be assignable without the prior
written consent of the other party, which consent will not be unreasonably
withheld.
11.03 Entire Agreement. This Agreement and the PDL/Roche Agreement
constitute the entire Agreement between the parties hereto with respect to the
within subject matter and supersede all previous Agreements, whether written
or oral. This Agreement shall not be changed or modified orally, but only by
an instrument in writing signed by both parties.
11.04 Severability. If any provision of this Agreement is declared
invalid by an arbitrator pursuant to Section 9.01 or by a court of last resort
or by any court or other governmental body from the decision of which an
appeal is not taken within the time provided by law, then and in such event,
this Agreement will be deemed to have been terminated only as to the portion
thereof which relates to the provision invalidated by that decision and only
in the relevant jurisdiction, but this Agreement, in all other respects and
all other jurisdictions, will remain in force; provided, however, that if the
provision so invalidated is essential to the Agreement as a whole, then the
parties shall negotiate in good faith to amend the terms hereof as nearly as
practical to carry out the original intent of the parties, and, failing such
amendment, either party may submit the matter to arbitration for resolution
pursuant to Section 9.01.
11.05 Indemnification. X. Xxxxx shall defend, indemnify and hold
harmless PDL, its trustees, officers, agents and employees harmless from any
and all liability, demands, damages, expenses, and losses of any kind,
including those resulting from death, personal injury, illness or property
damage arising (i) out of the manufacture, distribution, use, testing, sale or
other disposition, by X. Xxxxx, an Affiliate of X. Xxxxx, or any distributor,
customer, sublicensee or representative of X. Xxxxx or anyone in privity
therewith, of any Licensed Product, or any cell lines, their progeny, or other
biological materials provided by PDL pursuant to the PDL/Roche Agreement,
method, process, device or apparatus licensed or provided by PDL to X. Xxxxx
hereunder, or (ii) as a result of practicing a Joint Invention, or using PDL
Know-How or PDL Patents licensed to X. Xxxxx under this Agreement, except
where such claim is based on the negligent acts of commission or omission of
PDL.
11.06 Notices. Any notice or report required or permitted to be given
under this Agreement shall be in writing and shall be mailed by certified or
registered mail, or telexed or telecopied and confirmed by mailing, as follows
and shall be effective five (5) days after such mailing:
If to PDL:
Protein Design Labs, Inc.
0000 Xxxxxx Xxxxx
Xxxx Xxxx, Xxxxxxxxxx 00000
Attention: President
Copy to:
Xxxx Xxxx Xxxx & Freidenrich
000 Xxxxxxxx Xxxxxx
Xxxx Xxxx, Xxxxxxxxxx 00000-0000
Attn: Xxxxx X. Xxxxxxx, Esq.
If to X. Xxxxx:
X. Xxxxxxx - Xx Xxxxx & Co.
Limited Company
Xxxxxxxxxxxxxxxxx 000
XX-0000 Xxxxx, Xxxxxxxxxxx
Attention: Law Department
11.07 Choice of Law. The validity, performance, construction, and
effect of this Agreement shall be governed by the laws of the State of
California, United States of America.
11.08 Publicity. Both parties agree to issue mutual press releases
concerning their entry into this Agreement, with the content of such releases
to be approved in advance by both parties. In all other respects, neither
party shall use the name of the other party in any publicity release without
the prior written permission of such other party, which shall not be
unreasonably withheld. The other party shall have a reasonable opportunity to
review and comment on any such proposed publicity release. Except as required
by law, neither party shall publicly disclose the terms of this agreement or
its terms and conditions unless expressly authorized to do so by the other
party which authorization shall not be unreasonably withheld. In the event
that disclosure shall be agreed upon then the parties will work together to
develop a mutually acceptable disclosure.
11.09 Headings. The captions used herein are inserted for convenience
of reference only and shall not be construed to create obligations, benefits,
or limitations.
11.10 Counterparts. This Agreement may be executed in counterparts, all
of which taken together shall be regarded as one and the same instrument.
IN WITNESS WHEREOF, the parties have executed this Agreement to be
effective as of the Effective Date.
PROTEIN DESIGN LABS, INC.
By /s/ Xxxxxxxx Xxx Xxxx
Title: President
Date: 16 March 1989
X. XXXXXXXX-XX XXXXX & CO.
LIMITED COMPANY
By /s/ X. Xxxx. /s/ Pp Lunti
Title: Corporate Licensing Law Department
Date: March 16, 1989
Solely with respect to the granting of rights in Joint Roche-PDL Patents to X.
Xxxxx, Xxxxx hereby joins in this Agreement.
XXXXXXXX-XX XXXXX INC.
By /s/ Xxxxx Xxxxxx
Title: President and CEO
Date: March 16, 1989
APPENDIX A
Sole PDL Patents
T&T
DOCKET
NO. TITLE INVENTORS FILING DATE SERIAL NO. STATUS
11823-1 Closing and Tso and Queen Dec. 15, 1987 132,387 Pending
Expressions of
Phospholipase C
Genes
11823-4 IL-2 Receptor- Queen Apr. 15, 1988 182,682 Pending
Specific
Chimeric Antibodies
11823-5 Chimeric Antibody Queen Sep. 28, 1988 233,037 Pending
Production
11823-7 Cellular Toxic Queen Nov. 23, 1988 275,462 Pending
Conjugates
00000-0-0 Cellular Toxic Queen, Dec. 15, 1988 PCT/US88/ Pending
(Comb. of Conjugates Chovnick, (Canada & PCT 04493
`387 and Xxxxxxxxx and for Japan &
`462) Tso EPO)
00000-0-0 Cellular Toxic Queen, Dec. 28, 1988 290,968 Pending
(Comb. of Conjugates Chovnick,
`387 and Xxxxxxxxx and
`462) Tso
11823-8 Novel IL-2 Queen and Dec. 28, 1988 290,975 Pending
Receptor Specific Xxxxxxx
Human
Immunoglobulins
11823-9 Humanized Queen Feb. 13, 1989 310,252 Pending
Antibody
Production
APPENDIX B
EC Countries
Belgium
Denmark (including Iceland)
France
Germany
Greece
Ireland
Italy
Luxembourg
Netherlands
Portugal
Spain
United Kingdom (Scotland, England, Wales, Northern Ireland, Channel Islands,
Isle of Man)
As soon as it is perceivable that one country of the Territory may join
the EC or withdraw or become excluded from the EC, this APPENDIX B shall be
adapted accordingly.
