AMENDED AND RESTATED AGREEMENT
This Amended and Restated Agreement ("Amended and Restated Agreement")
is entered into as of October 20, 1999 ("Signing Date"), by and between X.
XXXXXXXX-XX XXXXX LTD of Basel, Switzerland ("X. Xxxxx") as successor to X.
Xxxxxxxx-Xx Xxxxx & Co. Limited Company, and PROTEIN DESIGN LABS, INC., a
Delaware corporation having offices at 00000 Xxxxxx Xxxxx, Xxxxxxx, Xxxxxxxxxx
00000, X.X.X. ("PDL").
RECITALS
X. X. Xxxxx and PDL are parties to an Agreement dated January 31, 1989, as
amended (the "1989 X. Xxxxx Agreement") pertaining to humanized and
chimeric antibodies against the interleukin-2 receptor ("IL-2R").
B. Under the 1989 X. Xxxxx Agreement, PDL exclusively licensed to X. Xxxxx
rights to a humanized antibody now known as Daclizumab (as defined below).
X. X. Xxxxx is currently marketing Daclizumab under the trademark Zenapax*
for the prevention of acute organ rejection in patients receiving kidney
transplants.
X. X. Xxxxx and PDL now desire to replace the 1989 X. Xxxxx Agreement with a
new agreement to provide PDL with rights to develop and, if successful,
promote or market Daclizumab in Autoimmune Indications (as defined below)
for increased compensation from the 1989 X. Xxxxx Agreement.
E. Concurrently with the entering into of this Agreement, PDL and Xxxxxxxx-Xx
Xxxxx Inc. ("Roche") are replacing an agreement addressing rights in the
United States of America similar to the 1989 X. Xxxxx Agreement (the "1989
PDL/Roche Agreement") with a new agreement covering both the United States
of America and Canada (the "1999 PDL/Roche Agreement") with respect to
which X. Xxxxx shall also be a party.
NOW, THEREFORE, in consideration of the premises and the mutual promises and
covenants set forth below, PDL and X. Xxxxx mutually agree to replace the 1989
X. Xxxxx Agreement as follows:
I. DEFINITIONS
For the purposes of this Agreement, the following terms, when written
with an initial capital letter (except as set forth in Sections 1.29 and
1.30), shall have the meaning ascribed to them below. All references to
particular Appendices, Articles and Sections shall mean the Appendices to, and
Articles and Sections of, this Agreement, unless otherwise specified.
1.1 "Affiliates" means any corporation or other business entity
controlled by, controlling, or under common control with another entity, 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.
1.2 "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.
1.3 "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 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. Humanized
anti-Tac is also known as "Daclizumab". "Daclizumab" as used in this Amended
and Restated Agreement means any product that contains Daclizumab.
1.4 "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 3.2 of the 1989 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 ROW Territory, where "major market" means either Japan or two of
the following three countries: France, Italy or the United Kingdom.
1.5 "Joint Inventions" means any inventions in the Field, whether
patented or not, which are jointly made during the period beginning on January
31, 1989 and ending upon expiration or termination of this Amended and
Restated Agreement 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 Roche or X. Xxxxx employee or person contractually required
to assign or license patent rights covering such inventions to Roche or X.
Xxxxx.
1.6 "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 Amended and
Restated Agreement, infringe a Valid Claim. Daclizumab shall be deemed to be
a Licensed Product.
1.7 "Net Transplant Sales" means either Total Sales (until such time
as Section 3A.4 applies) or Total Transplant Sales (beginning at such time as
Section 3A.4 applies), 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 [CONFIDENTIAL TREATMENT
REQUESTED] of the of the Total Sales or Total Transplant Sales, as
appropriate, to cover all other expenses or discounts, including but not
limited to customs duties, transportation and insurance charges and other
direct expenses.
1.8 "PDL Know-How" means, except as otherwise set forth in this
Section 1.8,
(a) all inventions, discoveries, trade secrets, information, experience,
data, formulas, procedures and results in the Field, and improvements thereon,
(collectively, "Know-How in the Field") 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 was rightfully held by PDL as of January 31, 1989, or
which was developed or acquired by PDL during the period beginning on January
31, 1989 and ending January 31, 1996 (such date representing the first (1st)
anniversary of the termination of the Research Program), and which Know-How in
the Field is required or useful for registration, manufacturing, using or
selling products in the Field, and
(b) all Know-How in the Field, including any information regarding the
physical, chemical, biological, toxicological, pharmacological, clinical, and
veterinary data, dosage regimens, control assays and specifications of
Daclizumab, which is rightfully held by PDL or its Affiliates as of the
Signing Date, or which is developed or acquired by PDL or its Affiliates with
the right to license or sublicense during the term of this Amended and
Restated Agreement, and which Know-How in the Field is required or useful for
registration, using or selling Daclizumab;
provided, however, that PDL Know-How excludes any Know-How in the Field of any
kind concerning generic methods of manufacturing (except as set forth in the
following paragraph) 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.
In the event Roche or X. Xxxxx manufactures a form or formulation of
Daclizumab for Autoimmune Indications under this Amended and Restated
Agreement that Roche or X. Xxxxx is not otherwise manufacturing for the
Transplant Indications, PDL Know-How shall also include all Know-How in the
Field which is rightfully held by PDL or its Affiliates as of the Signing
Date, or which is developed or acquired by PDL or its Affiliates with the
right to license or sublicense during the term of this Amended and Restated
Agreement, and which Know-How in the Field is required or useful for
manufacturing such form or formulation of Daclizumab for Autoimmune
Indications.
1.9 "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 Amended and Restated 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 or foreign
patent or inventor's certificate covering claims in the Field. "Queen et al.
Patents" mean those Sole PDL Patents in the ROW Territory claiming priority
under originally filed 12/28/89 as European application number 90903576.8 and
claiming priority under U.S. patent application serial nos. 290,975 filed
December 28, 1988 and 310,252 filed February 13, 1989.
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 ROW Territory.
1.11 "Research Program" means the collaborative scientific research
program between PDL and Roche which was completed in January 1995 and is
described more fully in the 1989 PDL/Roche Agreement.
1.12 "X. Xxxxx Inventions" means any inventions in the Field which are
made during the term of this Amended and Restated 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 ("U.S." or
"U.S.A." or "United States") and its territories and possessions where the
patent laws of the United States are in force, and Canada and its territories
and possessions. It is understood that the PDL/Roche Agreement comprises a
separate but complementary license agreement covering activities in the Roche
Territory.
1.14 "ROW Territory" means all countries of the world excluding the
Roche Territory. The ROW Territory shall not include any countries with
respect to indications in which X. Xxxxx grants an exclusive license to PDL
pursuant to Section 2.4.
1.15 "Valid Claim" means, as applicable, either (a) with respect to
royalties payable by X. Xxxxx to PDL under this Agreement, 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, or (b) with
respect to royalties payable by PDL to X. Xxxxx under this Agreement, a claim
in any issued patent within the Roche 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.
1.16 "Roche Know-How" means all inventions, discoveries, trade secrets,
information, experience, data, formulas, procedures and results specifically
related to Daclizumab, and improvements thereon (collectively, "Daclizumab
Know-How") including any information regarding the physical, chemical,
biological, toxicological, pharmacological, clinical, and veterinary data,
dosage regimens, control assays and specifications of Daclizumab, which is
rightfully held by X. Xxxxx or its Affiliates as of the Signing Date, or which
is developed or acquired by X. Xxxxx or its Affiliates with the right to
license or sublicense during the term of this Amended and Restated Agreement,
and which Daclizumab Know-How is required or useful for development of a
subcutaneous formulation for Daclizumab, and for using or promoting Daclizumab
for Autoimmune Indications.
In the event that pursuant to Section 2C.2, PDL obtains a right to
manufacture Daclizumab for Autoimmune Indications, Roche Know-How shall also
include all Daclizumab Know-How which is rightfully held by X. Xxxxx or its
Affiliates as of the Signing Date, or which is developed or acquired by X.
Xxxxx or its Affiliates with the right to license or sublicense during the
term of this Amended and Restated Agreement, and which Daclizumab Know-How is
required or useful for manufacturing Daclizumab.
1.17 "Roche Patents" means all patent applications owned or controlled
by Roche, X. Xxxxx or their Affiliates ("Sole Roche 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 Amended and Restated 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 or foreign patent or inventor's certificate covering claims in the
Field. "Sole Daclizumab Roche Patents" means those patents and applications
included within the Sole Roche Patents containing claims specifically related
to Daclizumab.
1.18 "Autoimmune Indications" means all indications that involve
pathogenic consequences, including tissue injury, produced by autoantibodies
or autoreactive T lymphocytes interacting with self epitopes, i.e.,
autoantigens. Autoimmune Indications shall include, without limitation,
psoriasis, rheumatoid arthritis, systemic lupus erythematosus, scleroderma,
juvenile rheumatoid arthritis, polymytosis, Type I diabetes, sarcoidosis,
Sjogrens syndrome, chronic active non-pathogenic hepatitis, non-infectous
uveitis (Behcets), aplastic anemia, regional non-pathogenic enteritis
(including ulcerative colitis, Crohn's Disease and inflammatory bowel
disease), Kawasaki's disease, post-infectious encephalitis, multiple
sclerosis, and tropic spastic paraparesis..
1.19 "Transplant Indications" means all indications that are not
Autoimmune Indications, including, without limitation, solid organ
transplantation (including tolerance induction and xenotransplantation), bone
marrow transplantation, graft versus host disease and cell transplantation.
In any event, should a given indication have applicability in both Autoimmune
Indications and transplantation, such indication shall be deemed a Transplant
Indication and not an Autoimmune Indication; provided that an Autoimmune
Indication shall not be deemed a Transplant Indication merely because it may
cause the need for a transplant (e.g., Type I diabetes, even if it causes the
need for an organ transplant).
1.20 "Total Sales" means the gross invoice price ("GIP") of all
Licensed Products for all indications sold or otherwise disposed of for
consideration by X. Xxxxx, its Affiliates or sublicensees (other than PDL and
its Affiliates) 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 rate of exchange at the time in
accordance with X. Xxxxx'x then current standard practices.
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, Total
Sales shall be determined by multiplying the Total 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 the sum of the
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 Total 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 Total Sales.
1.21 "Total Autoimmune Sales" means the difference of Total Sales minus
Total Transplant Sales.
1.22 "Total Transplant Sales" means the portion of Total Sales derived
from Transplant Indications.
1.23 "Net Autoimmune Sales" means Total Autoimmune Sales, 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[CONFIDENTIAL TREATMENT REQUESTED]
of the Total Autoimmune Sales to cover all other expenses or discounts,
including but not limited to cash discounts, customs duties, transportation
and insurance charges and other direct expenses.
1.24 "Net Sales" means the aggregate of Net Transplant Sales and Net
Autoimmune Sales.
1.25 "PDL Development Costs" means, for a given Autoimmune Indication,
[CONFIDENTIAL TREATMENT REQUESTED] of the worldwide development costs accrued
by PDL for the development of Daclizumab. All PDL Development Costs shall be
calculated in accordance with cost accounting methods consistently applied and
complying with generally accepted accounting principles, incurred by PDL
during a period commencing on the Signing Date and ending on the date of the
filing by X. Xxxxx of the first (1st) application for marketing approval for
that Autoimmune Indication in a Major Country. PDL Development Costs shall
not include any costs incurred by PDL for the purpose of manufacturing by PDL
of Daclizumab in bulk form, but shall include any costs incurred by PDL in
connection with formulation development and performance of formulation, fill
and finish, and related activities. All PDL Development Costs that apply to
multiple Autoimmune Indications (e.g., a subcutaneous formulation of
Daclizumab) until the date of filing by X. Xxxxx for marketing approval for an
Autoimmune Indication in a Major Country shall be allocated to the first
Autoimmune Indication to which such costs apply that X. Xxxxx elects to market
and sell, co-market or co-promote.
1.26 "PDL Net Sales" means the GIP of Daclizumab sold or otherwise
disposed of for consideration by PDL, its Affiliates or sublicensees (other
than X. Xxxxx and its Affiliates) to independent third parties not an
Affiliate of the seller after deducting, if not already deducted, from the
amount invoiced:
(a) the amounts actually allowed as volume or quantity discounts,
rebates, price reductions, returns (including withdrawals and recalls); and
(b) sales, excise and turnover taxes imposed directly upon and
actually paid by PDL, its Affiliates or sublicensees.
In addition, there shall be deducted, to the extent not already deducted
from the amount invoiced, an amount equal to [CONFIDENTIAL TREATMENT
REQUESTED] of the GIP to cover all other expenses or discounts, including but
not limited to cash discounts, custom duties, transportation and insurance
charges and other direct expenses.
In the case of Combination Products for which Daclizumab and each of the
other therapeutically active ingredients contained in the Combination Product
have established market prices when sold separately, PDL Net Sales shall be
determined by multiplying the PDL Net Sales for each such Combination Product
by a fraction, the numerator of which shall be the established market price
for Daclizumab, and the denominator of which shall be the sum of the
established market prices for Daclizumab 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 PDL Net Sales for Combination Products.
If PDL or its Affiliates or sublicensees receive non-cash consideration
for any units of Daclizumab 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
PDL, or as reasonably estimated by PDL if unknown, shall be included in the
definition of PDL Net Sales.
1.27 "Major Countries" means the United Kingdom, France, Germany, Italy
and Spain.
1.28 "Cost of Goods Sold" means the manufacturing cost of unformulated
bulk Daclizumab, calculated in accordance with reasonable cost accounting
methods consistently applied by a party for its other pharmaceutical products,
provided that such methods comply with generally accepted accounting
principles. Cost of Goods Sold shall include direct labor (including fringe
benefits), direct materials (including taxes and duties), and a reasonable
allocation of indirect labor and materials, facilities expense (including
occupancy costs and depreciation of property, plant and equipment),
administration costs and other costs allocable to the manufacturing process.
1.29 "documents" used as a verb, for example in Section 2A.5 and
similar uses, means provides factual or substantial support, which support may
include, among other things, expert opinion.
1.30 "cover" (including variations thereof such as "covering" or
"covered") as used for example in Article III and Article III-A, means that
the manufacture, use, sale or importation of a particular Licensed Product
would infringe a Valid Claim in the absence of rights under such patent(s).
The determination of whether a particular Licensed Product is covered by
particular Valid Claims shall be made on a country-by-country basis.
II. LICENSE GRANTS
2.1 License Grant to X. Xxxxx. Subject to Sections 2.3, 2.4 and 5.2,
PDL grants to X. Xxxxx and to X. Xxxxx'x Affiliates the sole and exclusive
right to the PDL Know-How and PDL Patents, but only to the extent necessary to
make, have made, use and sell Licensed Products in the Field within the ROW
Territory. For so long as X. Xxxxx is in compliance with its obligations
under Section 5.1, X. Xxxxx may sublicense the right to make, have made, use
and sell Licensed Products in the Field within the ROW Territory with respect
to Transplant Indications, provided that no such sublicense shall be granted
with respect to Autoimmune Indications without first obtaining PDL's written
consent, which consent shall not be unreasonably withheld or delayed. Any
such sublicense shall be subject to Section 3.5 hereof, and shall terminate
automatically if X. Xxxxx shall not have remedied or initiated steps to remedy
a breach of Section 5.1 hereof, in a manner reasonably satisfactory to PDL
within sixty (60) days after receipt by X. Xxxxx of notice of such breach from
PDL.
2.2 Identification of Patents. Set forth on Appendix A is a list
identifying patents or patent applications which comprise PDL Patents as of
the Signing Date. PDL shall update this list by delivering a supplement to
X. Xxxxx no less frequently than once per year during the term of this Amended
and Restated Agreement.
2.3 License Grant to PDL. X. Xxxxx grants to PDL and to PDL's
Affiliates the exclusive right to Daclizumab, Roche Know-How and Roche
Patents, PDL Know-How, and PDL Patents but only to the extent necessary to
import, make, have made and use Daclizumab for the purpose of conducting
development and seeking registration of Daclizumab in Autoimmune Indications
in the ROW Territory as contemplated by this Amended and Restated Agreement.
2.4 Contingent License Grants to PDL. Certain additional licenses are
granted by X. Xxxxx to PDL as described in Sections 2B.8, 2B.9, 2C.2(b) and
5.2 subject to the occurrence of certain conditions.
2.5 Sublicensing by PDL. Subject to the prior written consent of X.
Xxxxx, which consent shall not be unreasonably withheld or delayed, PDL shall
have the right to sublicense [CONFIDENTIAL TREATMENT REQUESTED] any exclusive
marketing rights of PDL under this Amended and Restated Agreement.
II-A. DEVELOPMENT FOR AUTOIMMUNE INDICATIONS
2A.1 Development Responsibility. On and after the Signing Date, PDL
shall be solely responsible at its sole cost and expense to develop Daclizumab
for Autoimmune Indications ("AI Development"), including, without limitation,
any further preclinical studies or formulation development (such as the
development of a subcutaneous formulation) deemed required or useful by PDL
for such AI Development. All data and information generated by such
activities shall be PDL Know-How and PDL shall have the right to publish such
data and information in accordance with Section 8.3(b).
2A.2 Transfer of Know-How.
(a) Transfer of PDL Know-How. During the term of this Amended and
Restated Agreement, PDL shall transfer within sixty (60) days of each June 30
and December 31, PDL Know-How which is required or useful for X. Xxxxx to
carry out its obligations under this Amended and Restated Agreement. PDL will
permit access by X. Xxxxx during the AI Development at reasonable times and
with reasonable frequency to the relevant scientific personnel of PDL, but in
any event not more than once per calendar quarter. PDL agrees to inform X.
Xxxxx on a timely basis of all results in the Field obtained by PDL during the
AI Development to the extent such results are required or useful for X. Xxxxx
to carry out its obligations under this Amended and Restated Agreement.
(b) Transfer of Roche Know-How.
(i) PDL and X. Xxxxx shall each immediately identify a person to
coordinate communications related to review of Roche Know-How by PDL
("Coordinators"). The Coordinators shall agree upon a period of time,
including the starting date of such period and duration of such period, during
which X. Xxxxx shall make Roche Know-How available for PDL's review. Such
period shall occur within ninety (90) days after the Signing Date.
PDL's review of Roche Know-How in accordance with this Section 2A.2(b)
shall occur during Roche's normal business hours and at an agreed upon site(s)
of Roche. During such review, PDL shall have the right to (i) copy such
available Roche Know-How as it deems required or useful and (ii) discuss the
available Roche Know-How with the relevant X. Xxxxx personnel. X. Xxxxx shall
use its commercially reasonable efforts to answer PDL's questions related to
the available Roche Know-How, but X. Xxxxx shall have no liability to PDL if
despite X. Xxxxx'x commercially reasonable efforts, it is unable to answer any
such questions to PDL's satisfaction; provided that X. Xxxxx will not
intentionally withhold from PDL any material and pertinent Roche Know-How.
It is understood that Roche Know-How may be embraced within documents
that contain information not specifically related to Daclizumab, including
information related to products of X. Xxxxx other than Daclizumab.
Accordingly, to the extent any given document within the scope of Roche Know-
How contains information not specifically related to Daclizumab, X. Xxxxx may
redact such information from the relevant document prior to PDL review
thereof. To the extent any given document within the scope of Roche Know-How
contains unredacted information not specifically related to Daclizumab, PDL
shall maintain such information as Confidential Information.
(ii) After the transfer of Roche Know-How pursuant to Section
2A.2(b)(i), upon written request by PDL, X. Xxxxx shall, within a reasonable
time, provide PDL with Roche Know-How as is required for AI Development by any
regulatory or governmental authority in the ROW Territory if and when such
Roche Know-How is located, but X. Xxxxx shall have no liability to PDL if
despite X. Xxxxx'x commercially reasonable efforts, it is unable to locate any
such Roche Know-How.
(iii) Subject to Section 5.1, in no event shall there be any obligation
on the part of X. Xxxxx to generate any new data or information related to
Licensed Products.
2A.3 Development Plan. Within sixty (60) days after the Signing Date,
PDL shall prepare and deliver to X. Xxxxx an AI Development plan, including
intended AI Development activities and budgets for each intended AI
Development activity. PDL shall update this plan by delivering a supplement
to X. Xxxxx from time to time during the term of this Amended and Restated
Agrement, provided that PDL shall in any event provide a supplement within
sixty (60) days of each December 31 during the term of this Amended and
Restated Agreement.
2A.4 Reports. PDL will provide X. Xxxxx within forty-five (45) days of
each June 30 and December 31 during the term of this Amended and Restated
Agreement, a written report summarizing for the preceding semi-annual period
all PDL AI Development activities, including publications. X. Xxxxx shall
provide reports on the activities of X. Xxxxx with respect to the development
and sales of Daclizumab in Transplant Indications and Autoimmune Indications,
if any, through the Joint Development Committee ("JDC") established pursuant
to the 1999 PDL/Roche Agreement. PDL shall present the AI Development plans
for the ROW Territory to the JDC.
2A.5 Decisions. PDL will make the final decision with respect to all
AI Development activities, except that X. Xxxxx will have the right to veto
(through the JDC and subject to the decision-making process applicable to the
JDC) any AI Development activity for which X. Xxxxx documents that such
activity is reasonably likely to have a material adverse impact on sales of
Daclizumab for Transplant Indications within the ROW Territory. PDL will not
undertake any AI Development activity for which X. Xxxxx documents that such
activity is reasonably likely to have a material adverse impact on sales of
Daclizumab for Transplant Indications within the ROW Territory.
2A.6 Certain Regulatory Matters.
(a) Clinical Trials. PDL shall have the right to file in PDL's name
Investigational New Drug Applications or corresponding filings in countries of
the ROW Territory ("INDs") for AI Development. X. Xxxxx shall, at no cost to
PDL, provide assistance required or useful to allow PDL to cross-reference X.
Xxxxx filings to allow PDL to carry out without delay any related clinical
trial in the ROW Territory. PDL shall advise and consult with X. Xxxxx with
respect to any significant issues or questions raised by any regulatory
authorities with respect to any such IND or related clinical trial. PDL shall
provide copies to X. Xxxxx of any such IND and any other records of
interactions with regulatory authorities (e.g., correspondence, minutes or
notes of telephone conferences or meetings, etc.) with respect to any such IND
or related clinical trials in a Major Country. PDL and X. Xxxxx, including
its Affiliates, shall each supply the other copies of all regulatory filings
in Major Countries related to the use of the clinical materials for AI
Development promptly after the time of such filings.
To the extent X. Xxxxx is required under applicable law, rule or
regulation, X. Xxxxx shall make all filings necessary to permit the use of the
clinical materials supplied by Roche or X. Xxxxx pursuant to Section 3C.1.
PDL and X. Xxxxx, including its Affiliates, shall each supply the other copies
of all regulatory filings related to the use of the clinical materials for AI
Development promptly after the time of such filings.
(b) Adverse Event Reporting. Each party shall notify the other of all
information coming into its possession concerning any and all side effects,
injury, toxicity, pregnancy or sensitivity reaction associated with commercial
or clinical uses, studies, investigations or tests with Daclizumab, throughout
the world, whether or not determined to be attributable to Daclizumab
("Adverse Event Reports"). The parties shall each identify a person to
coordinate the exchange of Adverse Event Reports ("Report Coordinators") so as
to enable timely reporting of such Adverse Event Reports to appropriate
government and regulatory authorities consistent with all laws, rules and
regulations. The Report Coordinators shall agree in writing upon formal
procedures for such exchange.
2A.7 Registration.
(a) PDL shall notify in writing ("Filing Notice") X. Xxxxx in the
event that PDL determines that any clinical trial results in an Autoimmune
Indication would justify filing by X. Xxxxx in any country in the ROW
Territory of an application for Regulatory Approval for such indication. The
Filing Notice shall be accompanied by (I) a list of countries in the ROW
Territory for which PDL is requesting such filing, (II) data and information
that PDL reasonably believes is sufficient to justify such filing, including
without limitation the clinical trial results in the specified Autoimmune
Indication, (III) the proposed labeling with respect to which PDL proposes
such filing, (IV) accrued PDL Development Costs through the most recent
calendar quarter for which PDL financial information is available prior to the
date of the Filing Notice and (V) an estimate of the PDL Development Costs to
be accrued through the expected date of first (1st) filing for Regulatory
Approval in a Major Country identified in the Filing Notice. In any event, X.
Xxxxx shall have the right to request, and PDL shall endeavor to timely supply
any existing additional data and information from PDL that X. Xxxxx believes
to be reasonably required or useful to make its decision to file or not to
file hereunder.
Within sixty (60) days after receipt by X. Xxxxx of the Filing Notice
(and accompanying information) ("Registration Review Period"), X. Xxxxx shall
notify PDL in writing with respect to each country specified in the Filing
Notice of whether X. Xxxxx (i) elects to make such a filing in that country,
(ii) desires to file in that country but reasonably believes that the clinical
trial results would not justify a filing by X. Xxxxx, including information in
reasonable detail setting forth the basis for such belief, or (iii) elects not
to make such a filing in that country (in which event X. Xxxxx'x rights to
make such filing and to market and sell Daclizumab in such country in the ROW
Territory for that Autoimmune Indication shall be deemed to revert to PDL as
provided in Section 2A.7(c)). If X. Xxxxx notifies PDL pursuant to (ii) of
the foregoing sentence, and if PDL disagrees with X. Xxxxx, then X. Xxxxx and
PDL shall submit the determination of whether the clinical trial results
support the labeling proposed by PDL in the countries identified in the Filing
Notice to an expert in regulatory matters ("Regulatory Arbiter"), including
expertise in the country(ies) in question. The Regulatory Arbiter shall be an
individual with not less than five (5) years of regulatory approval experience
for products for use in Autoimmune Indications in the country in question and
shall not have any preexisting or prior relationship with either of the
parties within the past five (5) years. If the parties are unable to agree
upon the Regulatory Arbiter within ten (10) business days, then each party
shall submit a list of up to three (3) individuals meeting the criteria
(including reasonable detail specifying the basis for why the individual is
appropriate to serve as the Regulatory Arbiter and a confirmation by the party
that such Arbiter is independent of the party submitting her/his name) to the
Administrator of the American Arbitration Association ("AAA Administrator") in
accordance with the AAA International Rules of Arbitration and the AAA shall
select an individual from the lists presented. The Regulatory Arbiter shall
make a final, binding determination with respect to the submitted matter with
respect to the countries in question within thirty (30) days of submission to
the Regulatory Arbiter hereunder. In the event that the Regulatory Arbiter
determines that the clinical trial results support the labeling proposed by
PDL in any of the countries identified in the Filing Notice, X. Xxxxx shall
have fifteen (15) business days from such determination to elect either
Section 2A.7(i) or (iii) in each such country. The parties shall each be
responsible for their respective costs for participation in the matter subject
to resolution by the Regulatory Arbiter and shall share equally the costs of
the Regulatory Arbiter.
For each country for which X. Xxxxx has elected to make such a filing,
X. Xxxxx or its Affiliates shall make such filing in all Major Countries and
Japan for which it has elected to proceed within the next ninety (90) day
period following the Registration Review Period, and in each other country for
which it has elected to proceed within the same time periods as would normally
be followed by X. Xxxxx for additional indications of its other approved
products, but in no event more than one hundred eighty (180) days after the
Registration Review Period. For each country in the ROW Territory for which
X. Xxxxx has either elected not to make such a filing, has failed to make an
election within the Registration Review Period, or has made such election but
has failed to make such filing within the period specified above, X. Xxxxx'x
rights to make such filing and to market and sell Daclizumab in such country
in the ROW Territory for that Autoimmune Indication shall be deemed to revert
to PDL as provided in Section 2A.7(c). In addition, if X. Xxxxx has elected
pursuant to Section 2B.2 to allow PDL to (a) co-market in a country in the ROW
Territory for a specified Autoimmune Indication, PDL and X. Xxxxx shall in the
first instance use commercially reasonable efforts to have X. Xxxxx make such
filing and permit PDL to cross-reference the X. Xxxxx filing in such country,
provided that if such procedure is not sufficient for PDL to market and sell
Daclizumab in such country in the ROW Territory for that Autoimmune
Indication, PDL shall have the right to make such filing in such country in
the ROW Territory for that Autoimmune Indication as provided in Section
2A.7(c) or (b) exclusively market and sell Daclizumab in a country in the ROW
Territory for a specified Autoimmune Indication, PDL shall have the right to
make such filing in such country in the ROW Territory for that Autoimmune
Indication as provided in Section 2A.7(c).
(b) If X. Xxxxx has elected pursuant to Section 2A.7(a) to file an
application for Regulatory Approval, PDL shall provide all assistance required
or useful to allow X. Xxxxx to carry out such filing without delay, including
supplying relevant clinical data and promptly preparing and making any
necessary regulatory filings relating to manufacture of Daclizumab if it is
intended for PDL to conduct any manufacturing steps. For each Major Country
and Japan in which X. Xxxxx has filed an application for Regulatory Approval
pursuant to Section 2A.7(a), X. Xxxxx shall diligently pursue the approval of
such application and shall advise and consult with PDL with respect to any
significant issues or questions raised by any regulatory authorities with
respect to such application. X. Xxxxx shall provide copies to PDL of all such
Major Country (and Japan) applications and any other records of interactions
with regulatory authorities relating to significant issues (e.g.,
correspondence, minutes or notes of telephone conferences or meetings, etc.)
with respect to such applications and Autoimmune Indications. X. Xxxxx shall
provide PDL with a quarterly summary and the status of all such applications,
including a summary of any significant issues and the strategy for dealing
with such issues. The parties shall discuss in good faith the labeling for
Daclizumab to be requested for Regulatory Approval in a Major Country for a
period not to exceed thirty (30) days from the date of notification from X.
Xxxxx that it elects to file for Regulatory Approval in a Major Country or
Japan pursuant to Section 2A.7(b). If the parties are unable to agree upon
the labeling to be requested during such thirty (30)-day period, the parties
shall mutually agree upon a third party arbiter ("Labeling Arbiter") within
ten (10) business days following determination of the parties to have the
matter submitted to the Labeling Arbiter. The Labeling Arbiter shall be an
individual with not less than five (5) years of marketing and/or regulatory
approval experience for products for use in Autoimmune Indications in the
country in question. If the parties are unable to agree upon the Labeling
Arbiter within ten (10) business days, then each party shall submit a list of
up to three (3) individuals meeting the criteria (including reasonable detail
specifying the basis for why the individual is appropriate to serve as the
Labeling Arbiter and a confirmation by the party that such Arbiter is
independent of the party submitting her/his name) to the AAA Administrator in
accordance with the AAA International Rules of Arbitration and the AAA shall
select an individual from the lists presented. The Labeling Arbiter shall
make a binding determination within thirty (30) days of the submission of the
matter to the Labeling Arbiter hereunder. The parties shall each be
responsible for their respective costs for participation in the matter subject
to resolution by the Labeling Arbiter and shall share equally the costs of the
Labeling Arbiter.
(c) For each Major Country and Japan for which the right to file an
application for Regulatory Approval has reverted to PDL pursuant to Section
2A.7(a) and with respect to which PDL elects to proceed with a filing for
Regulatory Approval, X. Xxxxx shall provide all assistance required or useful
to allow PDL to assume responsibility for and to carry out such filing without
delay, including execution of any and all documents to transfer such authority
and promptly preparing and making any necessary regulatory filings relating to
manufacture of Daclizumab. If PDL elects to proceed with such filing, PDL
shall diligently pursue the approval of such marketing applications and shall
advise and consult with X. Xxxxx with respect to any significant issues or
questions raised by any regulatory authorities with respect to such
applications. PDL shall provide copies to X. Xxxxx of all such Major Country
(and Japan) applications and any other records of interactions with regulatory
authorities relating to significant issues (e.g., correspondence, minutes or
notes of telephone conferences or meetings, etc.) with respect to such
applications.
(d) The costs of making any filing for Regulatory Approval for
Daclizumab in an Autoimmune Indication in a country in the ROW Territory shall
be allocated between the parties as follows: (i) if the parties are co-
marketing, the costs of making any filing shall be shared equally; (ii) if the
parties are co-promoting, then the costs of making any filing shall be borne
in accordance with the profit allocation specified in the co-promotion
arrangement; or (iii) if either party is exclusively marketing and selling,
then that party will bear all of the costs of making any filing.
II-B. COMMERCIALIZATION FOR AUTOIMMUNE INDICATIONS
2B.1 Transplant Indications. X. Xxxxx shall continue to be responsible
for all aspects of commercialization of Licensed Products for Transplant
Indications in the ROW Territory and shall pay royalties on Net Transplant
Sales as provided in Article III.
2B.2 Autoimmune Indications. For each country in the ROW Territory for
which X. Xxxxx has elected to file an application for marketing approval of an
Autoimmune Indication pursuant to Section 2A.7(b), X. Xxxxx shall notify PDL
within ninety (90) days after making such election to file whether, if such
application is approved, for that Autoimmune Indication in that country in the
ROW Territory, it elects:
(a) to market and sell Daclizumab exclusively (in which case, Sections
2B.4(a) and 2B.6 will apply),
(b) to co-promote Daclizumab exclusively with PDL (in which case,
Sections 2B.4(a) and 2B.7 will apply),
(c) to co-market Daclizumab with PDL (in which case, Sections 2B.4(b)
and 2B.8 will apply), or
(d) to license PDL exclusively to market and sell Daclizumab (in which
case, Sections 2B.4(b) and 2B.9 will apply).
For each country in the ROW Territory for which X. Xxxxx fails to
provide notice of such election within the time specified above, PDL shall
have the sole right to market and sell Daclizumab for that Autoimmune
Indication in that country in the ROW Territory in accordance with the
provisions of Sections 2B.4(b) and 2B.9.
2B.3 One Time Elections. It is understood and agreed that for each
Autoimmune Indication in a country in the ROW Territory, if X. Xxxxx does not
elect to file for approval under Section 2A.7(a)(iii) or to market and sell,
co-promote or co-market under Section 2B.2(a), (b) or (c), as the case may be,
for a specified Autoimmune Indication, then X. Xxxxx shall no longer have the
right to market and sell, co-promote or co-market Daclizumab in that country
in the ROW Territory for that Autoimmune Indication.
2B.4 Booking of Sales, Trademarks, Etc.
(a) For each Autoimmune Indication, for all countries in the ROW
Territory in which X. Xxxxx is exclusively promoting Daclizumab in that
country, or the parties are co-promoting Daclizumab in that country in the ROW
Territory, the parties intend (i) that X. Xxxxx shall be responsible at its
sole cost for booking all sales of Daclizumab and for distribution of
Daclizumab and, subject to Article II-C, that Roche and its Affiliates shall
be responsible for manufacturing Daclizumab and (ii) that Daclizumab will be
marketed under the trademark "Zenapax" or such other trademark as is selected
by X. Xxxxx. In those countries in the ROW Territory in which PDL co-promotes
Daclizumab, PDL shall act as a sales agent for X. Xxxxx and shall submit all
orders for Daclizumab to X. Xxxxx and its Affiliates.
(b) For each Autoimmune Indication, for all countries in the ROW
Territory in which PDL is exclusively promoting Daclizumab in that country in
the ROW Territory, or the parties are co-marketing Daclizumab in that country
in the ROW Territory, the parties intend (i) that each party shall be
responsible at its sole cost for booking its own sales of Daclizumab and for
its own distribution of Daclizumab, (ii) that manufacturing of Daclizumab will
be performed in accordance with Article II-C and (iii) that Daclizumab will be
marketed by each party under its own trademark. PDL acknowledges that
"Zenapax" is a trademark of X. Xxxxx and its Affiliates and agrees that any
PDL trademark for Daclizumab shall be selected using reasonable efforts to
avoid a trademark that is confusingly similar to "Zenapax". If one party is
manufacturing and selling supplies of Daclizumab to the other party, it shall
accept and fill such orders on a non-discriminatory basis relative to
accepting and filling orders from its own sales force.
2B.5 Information. In the event that X. Xxxxx elects to exclusively
market and sell Daclizumab for Autoimmune Indications in a Major Country, X.
Xxxxx shall provide to PDL regular, and in any event not less than semi-
annual, reports to PDL on X. Xxxxx'x efforts and plans to market and sell
Daclizumab in the Major Countries and on a summary basis for regions outside
of the Major Countries.
2B.6 Where X. Xxxxx Promotes Alone. For each country in the ROW
Territory for which X. Xxxxx has elected pursuant to Section 2B.2 to
exclusively market and sell Daclizumab for a specified Autoimmune Indication
(or for which PDL has elected not to exercise co-promotion or co-marketing
rights if X. Xxxxx has elected one of those options under Section 2B.2), X.
Xxxxx shall use commercially reasonable efforts to diligently market and sell
Daclizumab for that Autoimmune Indication in that country in the ROW
Territory. For each Major Country in the ROW Territory, X. Xxxxx shall
propose by November 1 of each year a budget for that country in the ROW
Territory to be spent on marketing and sales of Daclizumab for each Autoimmune
Indication in the following calendar year, for approval by the JCC (as defined
in Section 2B.7(b)) or if no JCC exists, by each of the parties. X. Xxxxx
shall deliver a report to PDL by March 31 of each year detailing the level of
sales and marketing expenditure for Daclizumab for each Autoimmune Indication
during the preceding calendar year for each Major Country in the ROW
Territory. [CONFIDENTIAL TREATMENT REQUESTED]
2B.7 Where X. Xxxxx and PDL Co-Promote.
(a) For each country in the ROW Territory for which X. Xxxxx has
elected pursuant to Section 2B.2 to co-promote Daclizumab with PDL for a
specified Autoimmune Indication, PDL shall notify X. Xxxxx within thirty (30)
days after receiving the notice under Section 2B.2 from X. Xxxxx of whether
PDL elects to co-promote Daclizumab for that Autoimmune Indication in that
country in the ROW Territory. The terms of the co-promotion arrangement shall
be negotiated and agreed to promptly after notice from PDL hereunder, but in
any event not later than ninety (90) days following delivery of such notice.
In any event, such co-promotion arrangement shall assume a sharing of co-
promotion, marketing and selling expenses [CONFIDENTIAL TREATMENT REQUESTED],
except as may be adjusted pursuant to Section 2B.7(b). If PDL elects not to
exercise such co-promotion rights for that Autoimmune Indication in that
country in the ROW Territory, then X. Xxxxx shall have the sole right to
market and sell Daclizumab for that Autoimmune Indication in that country in
the ROW Territory in accordance with Section 2B.6.
(b) Within thirty (30) days after the first election by X. Xxxxx under
Section 2B.2(b) to co-promote Daclizumab with PDL for an Autoimmune Indication
in a country in the ROW Territory, X. Xxxxx and PDL shall form a joint
commercialization committee (the "JCC") consisting of two representatives from
PDL and two representatives from X. Xxxxx. The JCC shall generally oversee
the co-promotion efforts relating to Daclizumab. With respect to such co-
promotion efforts, the JCC shall develop a joint marketing plan, including,
but not limited to, an operational budget, addressing such issues as training
materials, training, sampling, promotional materials, product presentation,
professional educational efforts and detailing. In the case in which the JCC
determines that it is deadlocked, each party shall thereafter within ten (10)
business days designate a representative at the Vice President level or higher
to discuss the dispute. The designated representatives shall arrange promptly
to meet and discuss in good faith a resolution of the dispute. If the
designated representatives are unable to resolve the matter in question within
thirty (30) days of the designation of the representatives, then to the extent
the matter affects any country in the ROW Territory in which X. Xxxxx is co-
promoting Daclizumab for the Autoimmune Indication in question, X. Xxxxx shall
have the final decision with respect to activities proposed to be conducted by
X. Xxxxx. Notwithstanding the foregoing, if the deadlock referenced above
relates to a budget for co-promotion, then although X. Xxxxx may make the
final decision, PDL shall have the right to decrease its [CONFIDENTIAL
TREATMENT REQUESTED]
(c) In each country in the ROW Territory for which PDL has elected to
co-promote Daclizumab for a specified Autoimmune Indication, PDL and X. Xxxxx
shall use commercially reasonable efforts to diligently market and sell
Daclizumab for that Autoimmune Indication in that country in the ROW
Territory. For each such country in the ROW Territory, the JCC, as provided
in Section 2B.7(b), shall mutually agree upon an annual marketing plan by
November 1 of each year which shall include a budget for that country in the
ROW Territory to be spent on marketing and sales of Daclizumab for that
Autoimmune Indication in the following calendar year. Each party shall
deliver a report to the other party by March 31 of each year detailing the
level of sales and marketing efforts for Daclizumab for that Autoimmune
Indication during the preceding calendar year for each such country in the ROW
Territory. If either party fails to expend [CONFIDENTIAL TREATMENT REQUESTED]
of the agreed upon expenditure by that party for any country in the ROW
Territory for two (2) consecutive calendar years, then the other party shall
have the option to solely promote Daclizumab in such country in the ROW
Territory for that Autoimmune Indication in accordance with Section 2B.6 or
2B.9, as the case may be, by notifying the party failing to meet its
expenditure obligations within ninety (90) days after receipt of the report
from the other party indicating such failure.
2B.8 Where X. Xxxxx and PDL Co-Market. For each country in the ROW
Territory for which X. Xxxxx has elected pursuant to Section 2B.2 to co-market
Daclizumab with PDL for a specified Autoimmune Indication, PDL shall notify X.
Xxxxx within thirty (30) days after receiving the notice under Section 2B.2
from X. Xxxxx of whether PDL elects to co-market Daclizumab for that
Autoimmune Indication in that country in the ROW Territory. If PDL elects not
to exercise such co-marketing rights for that Autoimmune Indication in that
country in the ROW Territory, then X. Xxxxx shall have the sole right to
market and sell Daclizumab for that Autoimmune Indication in that country in
the ROW Territory in accordance with Section 2B.6.
In each country in the ROW Territory for which PDL has elected to co-
market Daclizumab for a specified Autoimmune Indication, (a) PDL and X. Xxxxx
shall act independently with respect to their own marketing and sales of
Daclizumab for that Autoimmune Indication in that country in the ROW
Territory, (b) the provisions of Section 2B.4(b) shall apply and (c) PDL shall
automatically be granted a nonexclusive license under all Roche Patents, Roche
Know-How, PDL Patents and PDL Know-How to the extent required or useful for
the purposes of carrying out such PDL marketing and selling activities. X.
Xxxxx or its Affiliates will supply commercial supplies of Daclizumab to PDL
in accordance with Article II-C. Nothing in this Amended and Restated
Agreement shall be deemed to require the parties to share or provide any
information in contravention of any applicable law, rule or regulation.
2B.9 Where PDL Promotes Alone. For each country in the ROW Territory
for which X. Xxxxx has elected pursuant to Section 2B.2 to allow PDL to
exclusively market and sell Daclizumab for a specified Autoimmune Indication,
or has not elected to file for marketing approval pursuant to Section
2A.7(a)(iii), or for which the option for PDL to exclusively market and sell
Daclizumab pursuant to Section 2B.2, 2B.6 or 2B.7 has been triggered, if PDL
then exercises its option to be the sole marketing and selling party in that
country in the ROW Territory for that Autoimmune Indication, then PDL shall
use commercially reasonable efforts to diligently market and sell Licensed
Products for that Autoimmune Indication in that country in the ROW Territory.
For each country in the ROW Territory for which PDL has exercised its option
to be the exclusive marketing and selling party of Daclizumab for a specified
Autoimmune Indication, upon such exercise, (a) the provisions of Section
2B.4(b) shall apply and (b) PDL shall automatically be granted a nonexclusive
license under all Roche Patents, Roche Know-How, PDL Patents and PDL Know-How
to the extent required or useful for the purposes of carrying out such PDL
marketing and selling activities. In addition, X. Xxxxx or its Affiliates
will supply commercial supplies of Daclizumab to PDL in accordance with
Article II-C.
II-C. MANUFACTURING
2C.1 Clinical Supplies.
(a) Supply. Roche and its Affiliates have agreed and shall use
commercially reasonable efforts to provide clinical supplies of Daclizumab to
PDL for development for Autoimmune Indications in accordance with the 1999
PDL/Roche Agreement. Nothing herein shall be deemed to limit or extend the
obligations of Roche and X. Xxxxx and its Affiliates with respect to such
efforts.
(b) Formulations. In the event PDL requests Daclizumab in a
formulation that X. Xxxxx is not otherwise manufacturing for the Transplant
Indications, and X. Xxxxx supplies such form or formulation (rather than only
unformulated bulk Daclizumab), PDL shall pay to X. Xxxxx for such supplies an
amount equal to X. Xxxxx'x Cost of Goods Sold (which shall be zero (0) to the
extent provided without charge under the 1999 PDL/Roche Agreement) plus
[CONFIDENTIAL TREATMENT REQUESTED] of X. Xxxxx'x costs of performing such
formulation work. In any event, PDL shall not be obligated to have X. Xxxxx
perform such form or formulation work.
2C.2 Commercial Manufacturing.
(a) Supply. Subject to Section 2C.2(b), X. Xxxxx shall use
commercially reasonable efforts to ensure supply of requirements for
Daclizumab in one of the following forms if neither Roche nor X. Xxxxx
manufactures in the formulation desired by PDL for use or sale in the ROW
Territory: (a) finished product form or formulated bulk form, if Roche or X.
Xxxxx then manufactures in the formulation desired by PDL, or (b) unformulated
bulk form.
(b) PDL Right to Manufacture.
[CONFIDENTIAL TREATMENT REQUESTED]
(iii) Other Manufacturing Rights. Notwithstanding the foregoing, the
parties acknowledge and agree that if PDL exercises its right or obtains the
right to manufacture Daclizumab under Section 2.3(c) of the 1999 PDL/Roche
Agreement, X. Xxxxx hereby grants and PDL accepts a nonexclusive worldwide
license to import, make and have made Daclizumab in the ROW Territory.
(c) Transfer Pricing.
(i) In the event that PDL has either (A) the exclusive right to make
and have made Daclizumab for Autoimmune Indications, or (B) the right to
perform formulation, fill and finish work for the final product version of
Daclizumab for any indications, PDL shall use commercially reasonable efforts
to supply worldwide requirements for Daclizumab for those indications. In
such event, PDL shall transfer such Daclizumab to X. Xxxxx at a price
calculated as follows:
[CONFIDENTIAL TREATMENT REQUESTED].
(ii) If Roche or X. Xxxxx continues to supply Daclizumab to PDL and PDL
is booking sales in any country under this Amended and Restated Agreement,
then the parties shall negotiate in good faith to enter into a separate supply
agreement which shall provide for a price to PDL calculated as follows:
[CONFIDENTIAL TREATMENT REQUESTED]
For purposes of the foregoing calculation, references to X. Xxxxx shall mean
X. Xxxxx and its Affiliates, as applicable. The supply agreement shall also
include procedures for PDL submitting its requirements to Roche or X. Xxxxx
for all indications with respect to which PDL has the right to develop, market
and sell under this Amended and Restated Agreement. Such procedures shall
include PDL providing (a) annual non-binding forecasts of its requirements and
(b) firm purchase commitments a mutally acceptable period, but in any event
not less than six (6) months prior to the time the order must be delivered to
PDL by Roche or X. Xxxxx.
III. ROYALTIES ON TRANSPLANT SALES, ETC.
3.1 Royalties on Transplant Sales. Subject to Article III-A, X. Xxxxx
agrees to pay PDL royalties on Net Transplant Sales in the ROW Territory
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
sum of [CONFIDENTIAL TREATMENT REQUESTED] (such sum, the "Royalty Setting
Sales"), with the applicable royalty based on such Royalty Setting Sales
determined as follows:
Royalty Setting Sales ($ in
millions)
Royalty Rate
Up to and including
[CONFIDENTIAL TREATMENT
REQUESTED]
[CONFIDENTIAL TREATMENT
REQUESTED]
Up to and including
[CONFIDENTIAL TREATMENT
REQUESTED]
[CONFIDENTIAL TREATMENT
REQUESTED]
Up to and including
[CONFIDENTIAL TREATMENT
REQUESTED]
[CONFIDENTIAL TREATMENT
REQUESTED]
Amount in excess of
[CONFIDENTIAL TREATMENT
REQUESTED]
[CONFIDENTIAL TREATMENT
REQUESTED]
Over [CONFIDENTIAL TREATMENT
REQUESTED]
[CONFIDENTIAL TREATMENT
REQUESTED]
For purposes of computing aggregate annual worldwide Royalty Setting
Sales, the relevant portion of X. Xxxxx'x Net Sales in the ROW Territory will
be combined with the relevant portion of the Net Sales of X. Xxxxx'x
Affiliates and sublicensees for all countries outside of the ROW Territory.
This same understanding is being incorporated into the 1999 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 3.1(a) for Net Transplant 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 3.2 below, if neither of the Patentability Criteria
have been satisfied, then X. Xxxxx shall pay PDL a royalty rate of
[CONFIDENTIAL TREATMENT REQUESTED] of the Net Transplant Sales in the country
of sale for the duration of this Amended and Restated 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 3.1(a)
above.
(c) [CONFIDENTIAL TREATMENT REQUESTED]
(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 in the European Community, and such
presumption being conclusive as between the parties hereto with respect to
sales of such products made anywhere else within the ROW Territory.
Accordingly, X. Xxxxx shall pay PDL royalties on sales of each such product in
the ROW Territory (except for sales with respect to which the above rebuttable
presumption has in fact been refuted by X. Xxxxx) for a period of
[CONFIDENTIAL TREATMENT REQUESTED] from Initial Commercialization of such
product in accordance with the terms of this Section 3.1 or Article III-A, as
appropriate, and such sales shall constitute "Net Transplant Sales" if sold
for Transplant Indications or "Net Autoimmune Sales" if sold for Autoimmune
Indications.
3.2 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 [CONFIDENTIAL TREATMENT REQUESTED] 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 [CONFIDENTIAL TREATMENT REQUESTED]
following Initial Commercialization of such Licensed Product, then X. Xxxxx
shall pay PDL [CONFIDENTIAL TREATMENT REQUESTED] of the Net Transplant Sales
of such Licensed Product in the country of sale until the tenth 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 3.1(a) or (b) above, whichever is
applicable). Valid Claims and de facto exclusivity are to be determined on a
country-by-country basis.
3.3 Foreign Filing Expenses Credited Against Royalties. X. Xxxxx
shall have the right to credit [CONFIDENTIAL TREATMENT REQUESTED] of all
Transplant Foreign Filing Expenses (as defined in Section 5.3 below) actually
paid to PDL, less credits already taken under the 1989 X. Xxxxx Agreement,
against future royalties due to PDL pursuant to this Article III provided that
such credits, when added to the offset provided for in Section 3.4 below, may
not reduce the royalties to be paid to PDL to less [CONFIDENTIAL TREATMENT
REQUESTED] of the amount which would otherwise be due pursuant to Section 3.1
hereof.
3.4 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 ROW Territory and if PDL
and X. Xxxxx agree upon the terms of such license ("Third Party License"),
then the parties shall [CONFIDENTIAL TREATMENT REQUESTED]. 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 [CONFIDENTIAL
TREATMENT REQUESTED] sharing 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 3.1, 3.2 and 3A.4 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 3.1, 3.2 and 3A.4 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 3.1 to less [CONFIDENTIAL TREATMENT REQUESTED] of Net
Transplant Sales in any year, or under Sections 3.1(b) and 3.2 to less
[CONFIDENTIAL TREATMENT REQUESTED] if X. Xxxxx has de facto exclusivity and
[CONFIDENTIAL TREATMENT REQUESTED] if X. Xxxxx does not have de facto
exclusivity, and provided further, that X. Xxxxx'x total royalty obligations
to PDL under Sections 3.1 and 3.2 when added to those royalties payable to
third parties pursuant to Third Party Licenses [CONFIDENTIAL TREATMENT
REQUESTED] of Net Transplant Sales in any year.
3.5 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 xxxxx any sublicenses under this Amended and Restated
Agreement, then X. Xxxxx shall obtain the written commitment of such
sublicensees to abide by all applicable terms and conditions of this Amended
and Restated 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 Amended and Restated Agreement.
3.6 Royalties upon Termination. If this Amended and Restated
Agreement is terminated pursuant to Sections 7.2, 7.3 or 7.4 below, X. Xxxxx
shall continue to pay PDL any royalties earned pursuant to this Article III or
Article III-A prior to the date of termination and any royalties earned
thereafter as a result of sales under Section 7.5.
III-A. ROYALTIES AFTER AUTOIMMUNE APPROVAL
3A.1 Forecasts. To the extent permissible under applicable law, X.
Xxxxx shall provide forecast information regarding the estimated sales of
Daclizumab for an Autoimmune Indication in the ROW Territory as set forth in
this Section 3A.1; provided that if applicable laws prohibit the sharing of
such forecast information, the parties shall discuss in good faith an
alternative basis for calculating and verifying the Blended Rate (as defined
below) applicable for the Forecast Periods (as defined below) in question.
(a) Initial Forecast Period. Within sixty (60) days after the first
filing for Regulatory Approval of Daclizumab for an Autoimmune Indication in
the ROW Territory by X. Xxxxx or its Affiliates, X. Xxxxx shall provide PDL
[CONFIDENTIAL TREATMENT REQUESTED] (the "Initial Forecast Period") of the
following:
(i) if X. Xxxxx expects to elect to make the same election under
Section 2B.2(a), (b) or (c) for all countries of the ROW Territory
(including those countries not identified with the Filing Notice), then
X. Xxxxx'x best good faith estimate of its expected sales of Daclizumab
for the ROW Territory for that Autoimmune Indication for the Initial
Forecast Period (it being understood that such stated expectation shall
not be binding upon X. Xxxxx), or
(ii) if X. Xxxxx expects not to elect to make the same election under
Section 2B.2(a), (b) or (c) for all countries of the ROW Territory
(including those countries not identified with the Filing Notice), then
for each country in the ROW Territory, X. Xxxxx'x best good faith
estimate of when it would make an election under Section 2B.2 for that
Autoimmune Indication, which election it expects to make, and its
expected sales of Daclizumab in that country for that Autoimmune
Indication for the Initial Forecast Period (it being understood that
such stated expectation shall not be binding upon X. Xxxxx); and
(iii) X. Xxxxx'x best good faith estimate of its expected total Net
Transplant Sales for the ROW Territory and worldwide for all Licensed
Products for the Initial Forecast Period (it being understood that such
stated expectation shall not be binding upon X. Xxxxx).
(b) Subsequent Forecast Periods. The Initial Forecast Period shall end
upon the earliest of
(i) the end of the term specified in Section 3A.1(a),
(ii) the end of the calendar quarter during which Regulatory Approval
occurs for a second Autoimmune Indication for which X. Xxxxx has elected
to market and sell exclusively, co-promote or co-market Daclizumab under
Section 2B.2(a), (b) or (c), or
(iii) the end of the calendar quarter during which Regulatory Approval
occurs in a Major Country for the initial Autoimmune Indication for
which X. Xxxxx has elected to market and sell exclusively, co-promote or
co-market Daclizumab under Section 2B.2(a), (b) or (c) but had
previously not expected to make such election under Section 3A.1(a)(ii).
By way of clarification and without limitation, if X. Xxxxx specifies
that it expects to elect in all countries of the ROW Territory pursuant to
Section 3A.1(a)(i), then Section 3A.1(b)(iii) above shall not apply. By way
of illustration and without limitation, the following examples illustrate two
cases in which a new Blended Rate would apply due to the application of
Section 3(b)(iii):
(A) Example 1. If X. Xxxxx specifies pursuant to a Filing Notice that
it expects to elect in Switzerland, France and Germany pursuant to
Section 3A.1(a)(ii) (i.e., for less than all of the Major Countries),
and X. Xxxxx receives Regulatory Approval in the United Kingdom (i.e., a
Major Country in which X. Xxxxx did not expect to elect to market
exclusively, co-market or co-promote), then Section 3A.1(b)(iii) above
would apply and the Initial Forecast Period would end as of the date of
such Regulatory Approval in the United Kingdom.
(B) Example 2. If X. Xxxxx receives a Filing Notice only for
Switzerland and elects to file in Switzerland but specifies that it
expects not to make the same election in any or less than all of the
Major Countries pursuant to Section 3A.1(a)(ii), and X. Xxxxx thereafter
receives Regulatory Approval in a Major Country in which X. Xxxxx did
not expect to elect to market exclusively, co-market or co-promote, then
Section 3A.1(b)(iii) above would apply and the Initial Forecast Period
would end as of the date of such Regulatory Approval in the first Major
Country or in the first Major Country in which X. Xxxxx specified that
it would not make the same election as it made in Switzerland, as the
case may be.
Each subsequent Forecast Period (as defined below) shall begin upon the
end of the immediately preceding Forecast Period and shall end upon the
earliest of
(I) the end of [CONFIDENTIAL TREATMENT REQUESTED] quarters after the end
of the prior Forecast Period,
(II) the end of the calendar quarter during which Regulatory Approval
occurs for the next Autoimmune Indication for which X. Xxxxx has elected
to market and sell exclusively, co-promote or co-market Daclizumab under
Section 2B.2(a), (b) or (c) or
(III) the end of the calendar quarter during which X. Xxxxx elects to
file for Regulatory Approval in a Major Country for an Autoimmune
Indication with respect to which X. Xxxxx has previously elected to
market and sell exclusively, co-promote or co-market Daclizumab under
Section 2B.2(a), (b) or (c) in less than all Major Countries.
Each such period and the Initial Forecast Period are referred to as a
"Forecast Period".
Within sixty (60) days after the filing by X. Xxxxx or its Affiliates
for Regulatory Approval of Daclizumab for an additional Autoimmune Indication
in the ROW Territory or for an additional Major Country by X. Xxxxx or its
Affiliates (if such a filing is the triggering event of the end of a Forecast
Period) or within sixty (60) days prior to the end of the Forecast Period (if
it is to end [CONFIDENTIAL TREATMENT REQUESTED] after it began), X. Xxxxx
shall provide PDL with its best good faith estimates for the next Forecast
Period of the following:
(i) for each Autoimmune Indication for which X. Xxxxx has made an
election under Section 2B.2 (a), (b) or (c), if X. Xxxxx expects to
elect to make the same election for all countries of the ROW Territory
for that Autoimmune Indication, then X. Xxxxx'x best good faith estimate
of its expected sales of Daclizumab for the ROW Territory for that
Autoimmune Indication for the next Forecast Period (it being understood
that such stated expectation shall not be binding upon X. Xxxxx), or
(ii) for each Autoimmune Indication for which X. Xxxxx has made an
election under Section 2B.2 (a), (b) or (c), if X. Xxxxx expects not to
elect to make the same election under Section 2B.2 (a), (b) or (c) for
all countries of the ROW Territory, then for each country in the ROW
Territory, X. Xxxxx'x best good faith estimate of when it would make an
election under Section 2B.2 for that Autoimmune Indication (if not
already made), which election it expects to make, and its expected sales
of Daclizumab in that country for that Autoimmune Indication for the
next Forecast Period (it being understood that such stated expectation
shall not be binding upon X. Xxxxx), and
(iii) X. Xxxxx'x best good faith estimate of its expected total Net
Transplant Sales for the Territory and worldwide for all Licensed
Products for the next Forecast Period (it being understood that such
stated expectation shall not be binding upon X. Xxxxx).
3A.2 Blended Rate. Together with each forecast by X. Xxxxx delivered
under Section 3A.1, X. Xxxxx shall deliver a proposed royalty rate, as well as
the basis for its calculation, to be applied to all Net Sales of Licensed
Products in the ROW Territory during the corresponding Forecast Period by X.
Xxxxx, its Affiliates and sublicensees. Such rate shall take into account the
forecasted Net Transplant Sales and the applicable royalty rates under Section
3.1, forecasted Net Autoimmune Sales, Reimbursable Development Costs and
applicable royalty rates specified in Section 3A.3. PDL shall notify X. Xxxxx
within thirty (30) days after receipt of X. Xxxxx'x proposed royalty rate and
the basis for its calculation of whether it accepts such rate or not. If PDL
disagrees with the proposed rate, the parties each shall submit their proposed
rate to an arbiter in accordance with the procedures described in Section
3A.6(c). The royalty rate as accepted by PDL or determined by such arbiter
shall be the "Blended Rate" and shall be applied to Net Sales of Licensed
Products beginning with the first calendar quarter of the corresponding
Forecast Period. For purposes of the calculations hereunder, once X. Xxxxx'x
obligations to pay royalties to PDL have expired under Section 3.1(c), that
component of the calculation of the royalties on Net Transplant Sales for
purposes of calculating the Blended Rate shall be deemed to equal zero (0).
3A.3 Royalty Rates. For purposes of calculating the Blended Rate and
for performing the reconciliation under Section 3A.7, the following terms and
royalty rates shall apply:
(a) Transplant Sales. PDL shall be entitled to royalties on all Net
Transplant Sales at the rate calculated in accordance with Section 3.1.
(b) Autoimmune Sales, Development Costs. PDL shall be entitled to
reimbursement of and/or credit for the Reimbursable Development Costs by means
of a royalty on Net Autoimmune Sales at a higher "initial royalty rate" until
all Reimbursable Development Costs have been reimbursed to PDL and thereafter
at a "maintenance royalty rate" as described below. In the event that the
royalties for any Forecast Period are insufficient to fully reimburse PDL for
any and all Reimbursable Development Costs, PDL shall be entitled to a credit
in the subsequent Forecast Period for all such unreimbursed amounts. The
applicable royalty rates on Net Autoimmune Sales shall depend for each country
in the ROW Territory and for each Autoimmune Indication on whether X. Xxxxx
markets and sells exclusively or PDL co-promotes or co-markets with X. Xxxxx
and shall be determined as follows:
(i) Roche Markets Exclusively or Co-Markets. For each country in the
ROW Territory and each Autoimmune Indication, if X. Xxxxx markets and
sells exclusively or co-markets Daclizumab with PDL, Net Autoimmune
Sales by X. Xxxxx, its Affiliates and sublicensees for that Autoimmune
Indication in that country in the ROW Territory shall bear royalties to
PDL at an initial royalty rate of fifty percent (50%) and a maintenance
royalty rate of thirty-two percent (32%).
(ii) Roche and PDL Co-Promote. For each country in the ROW Territory
and each Autoimmune Indication, if X. Xxxxx and PDL co-promote
Daclizumab, Net Autoimmune Sales by X. Xxxxx, its Affiliates and
sublicensees for that Autoimmune Indication in that country in the ROW
Territory shall bear royalties to PDL at an initial royalty rate of
fifty percent (50%) and a maintenance royalty rate of forty percent
(40%). Such royalty rates assume a sharing of co-promotion expenses of
[CONFIDENTIAL TREATMENT REQUESTED] and shall be subject to adjustment in
the event of a different allocation between the parties as may be agreed
upon in accordance with Section 2B.7(b).
3A.4 Royalty Payments. Beginning with the calendar quarter in which
the first Regulatory Approval occurs for Daclizumab for an Autoimmune
Indication in the ROW Territory for which X. Xxxxx or its Affiliates has
elected to exclusively promote, co-promote or co-market Daclizumab, X. Xxxxx
shall pay royalties to PDL on all Net Sales of Licensed Products in the ROW
Territory at the Blended Rate, rather than at the rates specified in Article
III, except as adjusted pursuant to Section 3.4. X. Xxxxx shall provide
quarterly reports in accordance with the procedures outlined in Article IV.
3A.5 Reimbursable Development Costs. With respect to each Autoimmune
Indication, within thirty (30) days after the date of the first filing by X.
Xxxxx of an application for Regulatory Approval for that Autoimmune Indication
in a Major Country, PDL shall provide X. Xxxxx with the amount of PDL
Development Costs through the filing date for Regulatory Approval for that
Autoimmune Indication and for all other Autoimmune Indications to the extent
not previously reimbursed by X. Xxxxx. A portion of such costs ("Reimbursable
Development Costs") as calculated below shall be taken into account in setting
the Blended Rate pursuant to Section 3A.2, and shall be reimbursed to PDL
through the payments to be made to PDL pursuant to Section 3A.4. The
Reimbursable Development Costs shall be calculated by the formula
[CONFIDENTIAL TREATMENT REQUESTED]
[CONFIDENTIAL TREATMENT REQUESTED]
[CONFIDENTIAL TREATMENT REQUESTED]
[CONFIDENTIAL TREATMENT REQUESTED]
3A.6 Records. PDL agrees to keep and cause its Affiliates and third
parties acting on its behalf to keep full, clear and accurate records of the
Reimbursable Development Costs until reimbursed to PDL pursuant to Article
III-A, but in any event for a period of at least three (3) years or such
longer period as may coincide with PDL's internal record policy. PDL further
agrees to permit such books and records to be examined by an independent
accounting firm selected by X. Xxxxx from time to time to the extent necessary
to verify the PDL Development Costs. Unless X. Xxxxx obtains the prior
written consent of PDL, such accounting firms must be selected from among the
five (5) largest accounting firms in the Major Countries. Such examination is
to be made at the expense of X. Xxxxx, except in the event that the results of
the audit reveal a discrepancy in favor of PDL of [CONFIDENTIAL TREATMENT
REQUESTED] or more over the period being audited, in which case reasonable
audit fees for such examination shall be paid by PDL.
3A.7 Periodic Adjustment and Reconciliation.
(a) Within forty-five (45) days following the end of each Forecast
Period (including the Initial Forecast Period), X. Xxxxx shall provide PDL
with a written summary ("Proposed Allocation") covering for the ROW Territory
and for the entire immediately preceding Forecast Period the following:
(i) Total Sales and Net Sales,
(ii) the total Reimbursable Development Costs that has been
reimbursed to PDL through the Blended Rate royalty payments,
(iii) Net Transplant Sales by year and the applicable royalties
that would have applied as calculated under Article III,
(iv) Net Autoimmune Sales by country in the ROW Territory and by
Autoimmune Indication, and the applicable royalties that would
have applied in accordance with Section 3A.3,
(v) royalties paid by X. Xxxxx and PDL under Third Party Licenses
pursuant to Section 3.4,
(vi) the total royalties (i.e., the sum of clauses (iii) and (iv)
above) that otherwise would have been due to PDL for the
Forecast Period for Net Sales of Licensed Products in the ROW
Territory, and the difference of such amount less the actual
royalties paid to PDL for the Forecast Period through use of
the Blended Rate pursuant to Section 3A.4 (the "Reconciliation
Amount"), and
(vii) any additional information X. Xxxxx has available and may
be reasonably required or useful to determine the proposed
allocation.
PDL shall have a period of sixty (60) days after receipt to review X.
Xxxxx'x Proposed Allocation. During the review period, qualified
representatives of PDL and X. Xxxxx shall consult with one another to address
any questions regarding the preparation and detail of the summaries provided
pursuant to this Section 3A.7(a).
(b) PDL Agreement. If PDL does not object to X. Xxxxx'x Proposed
Allocation within such sixty (60)-day period, then X. Xxxxx shall, within ten
(10) business days following the earlier of (i) confirmation from PDL that it
does not object to the X. Xxxxx Proposed Allocation or (ii) the expiration of
the sixty (60)-day period, prepare a final reconciliation of Total Sales for
the Forecast Period in question, including the information listed in Section
3A.6(a). If the Reconciliation Amount is positive, such final reconciliation
shall be accompanied by payment of the Reconciliation Amount to PDL. If the
Reconciliation Amount is negative, then X. Xxxxx shall be entitled to a credit
equal to the Reconciliation Amount against future royalty payments to PDL,
provided that such credits, when added to any other offsets under this Amended
and Restated Agreement, may not reduce the royalties to be paid to PDL in any
period to less than [CONFIDENTIAL TREATMENT REQUESTED] of the royalties which
would otherwise be due to PDL for the Forecast Period. All Reimbursable
Development Costs not reimbursed to PDL for the applicable Forecast Period
shall be carried over to the subsequent Forecast Period and shall be taken
into account in calculating the Blended Rate for the subsequent Forecast
Period.
(c) PDL Disagreement. If PDL objects to X. Xxxxx'x Proposed
Allocation, then PDL shall reply in writing specifying its objection and PDL's
estimate of the appropriate allocation. Within ten (10) business days of the
written notice from PDL, each of the parties shall designate a representative
at the Vice President level or higher to discuss the disputed allocation. The
designated representatives shall arrange promptly to meet and discuss in good
faith a resolution of the dispute. If the designated representatives are
unable to resolve the matter in question within thirty (30) days of the
designation of the representatives, then PDL shall have thirty (30) days
thereafter to notify X. Xxxxx that it elects to have the matter submitted to
determination and/or audit by an independent third party (i.e., such third
party has not had a financial or other relationship with either party during
the preceding five (5) years) who is knowledgeable about marketing and sales
of pharmaceutical products in the transplant and/or Autoimmune Indications and
may also be an auditing organization ("Allocation Arbiter") and selected by
the parties' designated representatives. If the designated representatives
are unable to agree on an Allocation Arbiter within thirty (30) days of the
notification from PDL hereunder, the representatives shall each submit a list
of up to five (5) individuals whom the representative believes meets the
criteria set forth above to the Administrator of the American Arbitration
Association ("AAA Administrator") in accordance with the AAA International
Rules of Arbitration and the AAA shall select an individual from the lists
presented. The AAA Administrator shall select an individual from one of the
lists to serve as the Allocation Arbiter and such selection shall be binding
upon the parties.
If PDL fails to so notify X. Xxxxx, then PDL shall be deemed to have
agreed to X. Xxxxx'x Proposed Allocation and the parties shall proceed in
accordance with Section 3A.6(b). If PDL elects to submit the matter to the
Allocation Arbiter, each of the parties shall submit to and/or provide access
to the Allocation Arbiter all books and records of a party (including any
relevant surveys that may be conducted by or for a party for submission
hereunder) that the Allocation Arbiter deems reasonably required in order to
make a determination regarding the allocation hereunder. Such examination
and/or audit is to be made confidentially and at the expense of PDL, except in
the event that the Allocation Arbiter's determination reveals that X. Xxxxx'x
Proposed Allocation understated Net Sales or Net Autoimmune Sales by
[CONFIDENTIAL TREATMENT REQUESTED] or more, then the expense of the
examination and/or audit shall be paid by X. Xxxxx. The determination of the
Allocation Arbiter shall be final and binding on both parties for the Forecast
Period in question.
Within ten (10) business days following the resolution of any
disagreement regarding X. Xxxxx'x Proposed Allocation as provided under this
Section 3A.6(c), X. Xxxxx shall prepare a final reconciliation of Total Sales
for the Forecast Period in question, including the information listed in
Section 3A.6(a). If the Reconciliation Amount is positive, such final
reconciliation shall be accompanied by payment of the Reconciliation Amount to
PDL. If the Reconciliation Amount is negative, then X. Xxxxx shall be
entitled to a credit equal to the Reconciliation Amount against future royalty
payments to PDL, provided that such credits, when added to any other offsets
under this Amended and Restated Agreement, may not reduce the royalties to be
paid to PDL in any period to less than [CONFIDENTIAL TREATMENT REQUESTED] of
the total royalties which would otherwise be due to PDL. All Reimbursable
Development Costs not reimbursed to PDL for the applicable Forecast Period
shall be carried over to the subsequent Forecast Period and shall be taken
into account in calculating the Blended Rate for the subsequent Forecast
Period.
3A.7 Royalties to X. Xxxxx.
(a) Royalty Rate. In the event that PDL obtains rights under this
Amended and Restated Agreement to co-market with X. Xxxxx or to exclusively
market and sell Daclizumab for specified Autoimmune Indications in any
countries in the ROW Territory, PDL shall pay X. Xxxxx royalties on PDL Net
Sales of Daclizumab in those countries at a rate of eight percent (8%).
(b) Other Royalty Terms. In the event that PDL becomes obligated to
pay royalties to X. Xxxxx as provided in Section 3A.7(a), then the provisions
of Sections 3.4 (Offset for Third Party Licenses), 3.5 (Sublicenses), and 3.6
(Royalties upon Termination), and Article IV (Accounting and Payments) shall
be applied to such royalty payment obligation, with such changes as are
necessary to reflect that PDL would be the paying party and that PDL shall be
entitled to make calculations and payments in U.S. Dollars. If such event
occurs, the parties shall attempt for convenience to restate such provisions
and attach them to this Amended and Restated Agreement.
3A.8 [CONFIDENTIAL TREATMENT REQUESTED]
IV. ACCOUNTING AND PAYMENTS
4.1 Royalty Payments and Reports. Until such time as the first
exercise of its rights pursuant to Section 2B.2, X. Xxxxx shall make royalty
payments and written reports to PDL within forty-five (45) days after June 30
and December 31 of each year covering all sales of Licensed Products by X.
Xxxxx, its Affiliates or sublicensees for which invoices were sent during such
semi-annual period. Effective as of the first quarter following a semi-annual
period in which X. Xxxxx first exercises its rights pursuant to Section 2B.2,
X. Xxxxx agrees to make royalty payments and written reports to PDL within
forty-five (45) days after the end of each calendar quarter covering all sales
of Licensed Products by X. Xxxxx, its Affiliates or sublicensees for which
invoices were sent during such calendar quarter (provided that the first
quarter for which this occurs, such report shall cover all sales since the
last semi-annual report). Until such time as Section 3A.4 applies, 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 1.7 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 1.7 and Article III hereof.
After such time as Section 3A.4 applies, each report shall state:
(a) for Licensed Products disposed of by sale, the quantity and
description of Licensed Products, Total Sales, Net Sales, and
details of the calculation of such numbers by country in the ROW
Territory,
(b) if known or if estimates exist within X. Xxxxx, Net Transplant
Sales and Net Autoimmune Sales
(c) for Licensed Products disposed of other than by sale, the
quantity, description, and nature of the disposition, and
(d) the calculation of Reimbursable Development Costs and royalties
due to PDL for such quarter pursuant to Article III-A.
Subject to Section 11.9, 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. Concurrent
with the making of each quarterly report, X. Xxxxx shall include payment due
PDL of royalties for the calendar quarter 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 Amended
and Restated 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.
4.2 Termination Report. Roche also agrees to make a written report to
PDL within ninety (90) days after the date on which Roche, X. Xxxxx or their
Affiliates or sublicensees last sell a Licensed Product, stating in such
report the same information called for in each quarterly report by Section 4.1
for all Licensed Products and Combination Products made, sold or otherwise
disposed of and upon which were not previously reported to PDL.
4.3 Accounting. X. Xxxxx agrees to keep full, clear and accurate
records for a period of at least [CONFIDENTIAL TREATMENT REQUESTED] 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 4.1 and 4.2 above. Unless PDL obtains the prior written consent of
X. Xxxxx, such accounting firms must be selected from among the five largest
U.S. accounting 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 [CONFIDENTIAL TREATMENT REQUESTED] or more over the
period being audited, in which case reasonable audit fees for such examination
shall be paid by X. Xxxxx.
4.4 Methods of Payments.
(a) All payments due to PDL under this Amended and Restated Agreement
shall be paid in U.S. dollars by wire transfer to a bank in the U.S.
designated in writing by PDL. Whenever for the purpose of calculating
royalties conversion from any foreign currency shall be required, such
conversion shall be made as follows :
(i) when calculating the Total Sales and Net Sales, the amount of such
sales in foreign currencies shall be converted into Swiss Francs at the
average rate of exchange at the time for the applicable calendar quarter for
the countries concerned in accordance with X. Xxxxx'x then current standard
practices (which practices shall be reasonably documented in the report with
respect to which such conversion applies),
(ii) when converting the royalties on Net Sales calculated in Swiss
Francs, the conversion shall be at the average rate of the Swiss Franc to the
U. S. dollars at the time for the applicable calendar quarter in accordance
with X. Xxxxx'x then current standard practices (which practices shall be
reasonably documented in the report with respect to which such conversion
applies), and
(iii) in the case of sales by sublicensees, using the exchange rates
provided for in the written agreements between the sublicensee and X. Xxxxx
(which rates shall be reasonably documented in the report with respect to
which such conversion applies).
(b) All payments due from PDL to X. Xxxxx under this Amended and
Restated Agreement shall be paid in U.S. dollars by wire transfer to a bank
designated in writing by X. Xxxxx. If any currency conversion shall be
required in connection with payments by PDL to X. Xxxxx, such conversion shall
be made (i) by using the average of the daily exchange rates for such currency
quoted by Citibank, N.A. for each of the last five (5) business days of each
calendar quarter, or any other source otherwise agreed upon in writing by the
parties, and (ii) in the case of sales by sublicensees, using the exchange
rates provided for in the written agreements between the sublicensee and PDL
(which rates shall be reasonably documented in the report with respect to
which such conversion applies).
4.5 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 ROW Territory, the
parties shall confer regarding possible alternative arrangements to lawfully
avoid such withholding. If, between a country in the ROW 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
[CONFIDENTIAL TREATMENT REQUESTED] 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 of
the European Community.
All amounts owed under this Amended and Restated Agreement shall be paid
net of all applicable taxes, fees, and other charges, excluding only taxes on
a party's income. Any taxes on payments due hereunder which PDL or any of
its Affiliates or sublicensees shall be required by law to withhold or pay on
remittance of the royalty payments shall be deducted from the royalty payable
to X. Xxxxx. In such event, PDL shall furnish to the recipient copies of all
official receipts for such taxes and provide reasonable assistance in
obtaining a refund or credit for such taxes withheld.
4.6 Currency Transfer Restrictions. If in any country in the ROW
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 5.1
below.
V. CERTAIN COVENANTS OF X. XXXXX
5.1 Diligence. From and after the Signing Date, X. Xxxxx shall use
reasonable diligence in proceeding with registering, marketing and selling
Licensed Products within the ROW Territory. Reasonable diligence as used in
this Amended and Restated 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 ROW Territory, and it is understood that the exercise
by X. Xxxxx of reasonable diligence is to be determined by judging its efforts
in the ROW Territory taken as a whole. Notwithstanding the foregoing
sentence, if X. Xxxxx elects to proceed with a registration in any country in
the ROW Territory pursuant to Section 2A.7, then X. Xxxxx shall proceed with
reasonable diligence in filing for Regulatory Approval for the specified
Autoimmune Indication in that country in the ROW Territory. Further, if X.
Xxxxx elects to market Daclizumab for an Autoimmune Indication, either
exclusively or as a co-promotion or co-marketing arrangement with PDL, then X.
Xxxxx shall not position Daclizumab vis a vis its other products to the
detriment of sales of Daclizumab. If X. Xxxxx fails to exercise such
diligence, PDL may terminate this Amended and Restated Agreement and
X. Xxxxx'x rights hereunder pursuant to Section 7.4 below.
5.2 Initial ROW Territory Review.
(a) Initial Review. Promptly following the Signing Date, X. Xxxxx will
review its plans for obtaining marketing approvals and launching Daclizumab
for Transplant Indications in the countries of the ROW Territory. For any
countries in which X. Xxxxx does not have definite plans, supported by ongoing
activities to carry out those plans, both to obtain Regulatory Approval and to
launch Daclizumab for Transplant Indications, X. Xxxxx will notify PDL within
sixty (60) days after the Signing Date of the identity of such countries and,
with respect to each such country, whether X. Xxxxx elects (i) to return all
rights to Daclizumab to PDL for all indications, or (ii) to seek a sublicensee
of X. Xxxxx'x rights to Daclizumab. For each country for which X. Xxxxx
elects to seek a sublicensee, if X. Xxxxx has not entered into a sublicense
agreement for Daclizumab for that country within[CONFIDENTIAL TREATMENT
REQUESTED] after the Signing Date, all rights to Daclizumab for all
indications in that country in the ROW Territory shall then immediately and
automatically revert to PDL.
(b) Ongoing Review. For any countries in the ROW Territory for which
X. Xxxxx determines in its review pursuant to Section 5.2(a) that it has
specific plans, supported by ongoing activities to carry out those plans, to
obtain Regulatory Approval and to launch Daclizumab for Transplant
Indications, if X. Xxxxx subsequently determines not to carry out such plans
or ceases to actively carry out the activities necessary to achieve such
plans, then X. Xxxxx shall promptly notify PDL, with respect to such
country(ies) of whether it elects (i) to return all rights to Daclizumab to
PDL for all indications, or (ii) to seek a sublicensee of X. Xxxxx'x rights to
Daclizumab. For each country in the ROW Territory for which X. Xxxxx elects
to seek a sublicensee, if X. Xxxxx has not entered into a sublicense agreement
for Daclizumab for that country within six (6) months after such notice to
PDL, all rights to Daclizumab for all indications in those countries in the
ROW Territory shall then immediately and automatically revert to PDL.
(c) Reversion to PDL. For each country in the ROW Territory for which
all rights to Daclizumab have been returned or reverted to PDL pursuant to
this Section 5.2, PDL shall thereafter have the exclusive right to use, market
and sell Daclizumab for all indications in that country in the ROW Territory,
including the right to sublicense such rights to a sublicensee of PDL's choice
without any further compensation to X. Xxxxx, subject to X. Xxxxx'x consent,
which shall not be unreasonably withheld or delayed. Manufacturing and supply
of Daclizumab to PDL and regulatory matters shall be governed by Article II-C
and Section 2A.6 of this Amended and Restated Agreement in the same manner as
intended for countries in the ROW Territory in which PDL would obtain the
exclusive right to market and sell Daclizumab for Autoimmune Indications.
5.3 Reimbursement for Costs of Patent Applications for Transplant
Indications. For purposes of Sections 5.3 and 5.4, references to ROW Territory
shall also include Canada, including its territories and possessions.
(a) Right to Reimbursement. In any country in the ROW Territory
X. Xxxxx agrees to reimburse PDL for all ex parte out-of-pocket expenses
incurred by PDL after January 31, 1989 in connection with the prosecution and
maintenance in the ROW Territory of patent applications and patents included
within the PDL Patents or Joint Roche-PDL Patents for which PDL has made or
makes filings with respect to Transplant Indications pursuant to Article IX of
the 1999 PDL/Roche Agreement ("Transplant 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 Transplant Foreign Filing Expenses exceeding an aggregate of
[CONFIDENTIAL TREATMENT REQUESTED] in any calendar year.
(b) Consultation. Prior to the filing of a patent application for
Transplant Indications in the ROW 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 related
to Transplant Indications in the ROW 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. In any event, all patent
applications filed prior to the Signing Date pursuant to Section 5.02 of the
1989 X. Xxxxx Agreement shall be considered filings with respect to Transplant
Indications.
(c) Credit. X. Xxxxx shall be entitled to a credit for Transplant
Foreign Filing Expenses against royalties payable hereunder as provided in
Section 3.3 hereof.
5.4 Reimbursement for Costs of Patent Applications for Autoimmune
Indications.
(a) Accrual. PDL shall be responsible for all ex parte out-of-pocket
expenses incurred by PDL after the Signing Date in connection with the
prosecution and maintenance in the ROW Territory of patent applications and
patents included within the PDL Patents or Joint Roche-PDL Patents for which
PDL makes filings with respect to Autoimmune Indications pursuant to
Article IX of the 1999 PDL/Roche Agreement ("Autoimmune Foreign Filing
Expenses"), which Autoimmune Foreign Filing Expenses shall be calculated as
the sum of the following amounts:
(i) if such Autoimmune Foreign Filing Expenses are applicable to PDL
Patents or Joint Roche-PDL Patents with claims that cover an Autoimmune
Indication with respect to which X. Xxxxx elects either 2B.2(a), (b) or
(c), then PDL shall be entitled to reimbursement of [CONFIDENTIAL
TREATMENT REQUESTED] of all ex parte out-of-pocket expenses incurred by
PDL with respect to those patents and patent applications (to the extent
not previously reimbursed); plus
(ii) if such Autoimmune Foreign Filing Expenses are applicable to PDL
Patents or Joint Roche-PDL Patents with claims that cover an Autoimmune
Indication with respect to which X. Xxxxx has not yet elected either
2B.2(a), (b) or (c), then PDL shall be entitled to reimbursement of
[CONFIDENTIAL TREATMENT REQUESTED] of all ex parte out-of-pocket
expenses incurred by PDL with respect to those patents and patent
applications (to the extent not previously reimbursed); plus
(iii) if such Autoimmune Foreign Filing Expenses are applicable to PDL
Patents or Joint Roche-PDL Patents with claims that cover an Autoimmune
Indication with respect to which X. Xxxxx has notified PDL in writing
that it will not elect either 2B.2(a), (b) or (c), then PDL shall be
entitled to no reimbursement of ex parte out-of-pocket expenses incurred
by PDL with respect to those patents and patent applications.
(b) Reimbursement Following Election. Following reimbursement to PDL
pursuant to Section 3A.5 for an Autoimmune Indication with respect to which X.
Xxxxx elects either 2B.2(a), (b) or (c), PDL shall be reimbursed on an ongoing
basis one hundred percent (100%) of all ex parte out-of-pocket expenses
incurred by PDL with respect to prosecution and maintenance of the PDL Patents
or Joint Roche-PDL Patents containing claims that cover that Autoimmune
Indication. PDL shall invoice X. Xxxxx for such amounts on a quarterly basis
and payment from X. Xxxxx shall be made to PDL within thirty (30) days of
receipt of invoice from PDL.
(c) Limit on Reimbursement to PDL. In any event, X. Xxxxx shall not
be obligated to reimburse PDL pursuant to Sections 5.4 (a) or (b) for any
Autoimmune Foreign Filing Expenses exceeding an aggregate of [CONFIDENTIAL
TREATMENT REQUESTED] in any calendar year.
(d) PDL Control. PDL shall have full control over the strategy and
decisions with respect to the filing of any patent applications and patents
related to Autoimmune Indications in the ROW Territory. X. Xxxxx agrees to
cooperate with and reasonably assist PDL in the preparation of any patent
applications and the maintenance of any patents. If X. Xxxxx elects any of
its rights pursuant to Section 2B.2(a), (b) or (c), PDL shall regularly advise
X. Xxxxx of any substantial action or development in the prosecution of its
patent applications and patents related to Transplant Indications in the
relevant countries in the ROW Territory, in particular advising X. Xxxxx of
the scope of, the issuance of, the rejection of, or an opposition to any
respective patent application or patent related to Autoimmune Indications with
respect to which X. Xxxxx has exercised its rights.
VI. OWNERSHIP OF TECHNOLOGY
6.1 PDL Technology. Ownership of the PDL Know-How and PDL Patents
shall remain vested at all times in PDL. Notwithstanding the provisions of
Section 2.1, PDL expressly reserves under this Amended and Restated Agreement
(i) all rights to use the PDL Know-How, PDL's rights under any Joint Roche-PDL
Patents and 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,
PDL's rights under any Joint Roche-PDL Patents and PDL Patents for PDL's
internal research purposes in the Field, and as specified in Sections 2.3 and
2.4.
6.2 Joint Inventions and Joint Roche-PDL Patents. Ownership of Joint
Inventions and Joint Roche-PDL Patents shall be vested jointly in PDL and X.
Xxxxx. Except as expressly provided in this Amended and Restated Agreement, X.
Xxxxx shall have the exclusive right within the Territory during the term of
this Amended and Restated Agreement to make, have made, use or sell any Joint
Invention in the Field under any Joint Roche-PDL Patent. In any event, both
parties shall have the nonexclusive right within the Territory during the term
of this Amended and Restated Agreement to make, have made, use or sell any
Joint Invention outside the Field under any Joint Roche-PDL Patent, and
neither party shall be obligated to account to the other. Upon the expiration
or termination of this Amended and Restated Agreement, both parties shall have
the nonexclusive right to make, have made, use or sell any Joint Invention
under any Joint Roche-PDL Patent without restriction and without any
obligation to account to the other party. Notwithstanding the foregoing or
the provisions of Section 2.1, PDL expressly reserves the right to use any
Joint Invention under any Joint Roche-PDL Patent for PDL's internal research
purposes in the Field, and as specified in Sections 2.3 and 2.4.
6.3 X. Xxxxx Inventions. PDL hereby acknowledges that this Amended
and Restated Agreement does not grant PDL any ownership rights in the X. Xxxxx
Inventions. X. Xxxxx hereby confirms the rights of PDL to certain contingent
license grants to Roche Patents, Roche's rights under Joint Roche-PDL Patents
and Roche Know-How as provided in this Amended and Restated Agreement.
VI-A. ENFORCEMENT OF PATENTS
6A.1 Sole Patents.
(a) In the event of any action against a third party for infringement
of any claim in any issued patent in the ROW Territory within the Sole PDL
Patents or Sole Daclizumab Roche Patents, as the case may be, or the
institution by a third party of any proceedings for the revocation of any such
claim, each party will notify the other promptly and, following such
notification, the parties shall confer. PDL shall have the right, but shall
not be obligated, to prosecute such actions or to defend such proceedings
involving the Sole PDL Patents at its own expense, in its own name and
entirely under its own direction and control. X. Xxxxx shall have the right,
but shall not be obligated, to prosecute such actions or to defend such
proceedings involving the Sole Daclizumab Roche Patents, at its own expense,
in its own name and entirely under its own direction and control.
(b) If a party with the first right hereunder elects not to prosecute
any action for infringement or to defend any proceeding for revocation of any
claims in any issued patent in the ROW Territory within the Sole PDL Patents
or Sole Daclizumab Roche Patents, as the case may be, within ninety (90) days
of being requested by the other party to do so, the other party may prosecute
such action or defend such proceeding at its own expense, in its own name and
entirely under its own direction and control.
(c) In any event, the party bringing an action ("acting party")
pursuant to this Section 6A.1 shall solicit, and seriously consider in good
faith the non-acting party's input with respect to all material aspects of
such action, including without limitation, the development of the litigation
strategy and the execution thereof. In furtherance and not in limitation of
the foregoing, the acting party shall keep the other party promptly and fully
informed of the status of any such action, and the non-acting party shall have
the right to review and comment upon the acting party's activities related
thereto.
(d) Each party will reasonably assist the acting party in any such
action or proceeding being prosecuted or defended by the acting party, if so
requested by the acting party or required by law. The acting party will pay
or reimburse the assisting party for all costs, expenses and liabilities which
the assisting party may incur or suffer in affording assistance to such
actions or proceedings. No settlement of any such action or defense which
restricts the scope or affects the enforceability of PDL Know-How or Sole PDL
Patents may be entered into by either PDL or X. Xxxxx without the prior
consent of the other party hereto, which consent, in the case of X. Xxxxx
shall not be unreasonably withheld and in the case of PDL may be withheld in
PDL's sole and absolute discretion. No settlement of any such action or
defense which restricts the scope or affects the enforceability of Roche Know-
How or Sole Daclizumab Roche Patents may be entered into by either PDL or X.
Xxxxx without the prior consent of the other party hereto, which consent, in
the case of PDL shall not be unreasonably withheld and in the case of X. Xxxxx
may be withheld in X. Xxxxx'x sole and absolute discretion.
(e) If either party elects to prosecute an action for infringement or
to defend any proceedings for revocation of any claims pursuant to this
Section 6A.1 and subsequently ceases to continue or withdraws from such action
or defense, it shall forthwith so notify the other party in writing and the
other party may substitute itself for the withdrawing party and the parties'
respective rights and obligations under this Section 6A.1 shall be reversed.
6A.2 Joint Roche-PDL Patents. In the event of any action against a
third party for infringement of any claim in any issued patent in the ROW
Territory within the Joint Roche-PDL Patents, or the institution by a third
party of any proceedings for the revocation of any such claim, each party will
notify the other promptly and, following such notification, the parties shall
confer to determine whether either or both parties shall control the
prosecution or defense of such action or proceeding and who shall bear the
costs thereof. If the parties are unable to reach agreement within ninety
(90) days of the notification referred to above, then each party shall have
the right to bring such action or defend such proceeding at its own expense,
in its own name and entirely under its own direction and control; provided,
however, that if both parties elect to prosecute or defend, each party shall
bear its own expenses but both parties shall have equal control over such
prosecution or defense. No settlement of any action or defense which
restricts the scope or affects the enforceability of Joint Roche-PDL Patents
may be entered into by either PDL or X. Xxxxx without the prior consent of the
other party hereto, which consent shall not be unreasonably withheld. In any
event, the party bringing an action ("acting party") pursuant to this Section
6A.2 shall solicit, and seriously consider in good faith the other party's
input with respect to all material aspects of such action, including without
limitation, the development of the litigation strategy and the execution
thereof. In furtherance and not in limitation of the foregoing, the acting
party shall keep the other party promptly and fully informed of the status of
any such action, and the other party shall have the right to review and
comment upon the acting party's activities related thereto.
6A.3 Distribution of Proceeds. In the event either party exercises the
rights conferred in Section 6A.1 or 6A.2 hereof, and recovers any damages or
other sums in such action, suit or proceeding or in settlement thereof, such
damages or other sums recovered, shall first be applied to all costs and
expenses connected therewith including reasonable attorneys' fees, necessarily
involved in the prosecution and/or defense of any suit or proceeding, and if
after such reimbursement any funds shall remain from such damages or other
sums recovered, said recovery shall belong to the party exercising its rights;
provided, however, that any remaining recovery by shall be shared
[CONFIDENTIAL TREATMENT REQUESTED].
6A.4 Defense of Infringement Actions.
(a) X. Xxxxx shall defend at its own cost any infringement suit that
may be brought against PDL or X. Xxxxx on account of the development,
manufacture, production, use or sale of any Licensed Product by X. Xxxxx in
the ROW Territory, and shall indemnify and save PDL harmless against any such
patent or other infringement suits, and any claims, losses, damages,
liabilities, expenses, including reasonable attorneys' fees and cost, which
may be incurred by PDL therein or in settlement thereof. Any and all
settlements which restrict the scope or enforceability of PDL Know-How or PDL
Patents must be approved by PDL in its sole and absolute discretion before
execution by X. Xxxxx. Any and all settlements which restrict the scope or
enforceability of Joint Roche-PDL Patents must be approved by PDL before
execution by X. Xxxxx, such approval not to be unreasonably withheld. PDL
shall not be required to approve any settlement which does not include as a
condition thereof the granting to PDL of a full and unconditional release of
claims.
(b) PDL shall defend at its own cost any infringement suit that may be
brought against X. Xxxxx or PDL on account of the development, manufacture,
production, use or sale of Daclizumab in the ROW Territory by PDL, and shall
indemnify and save X. Xxxxx harmless against any such patent or other
infringement suits, and any claims, losses, damages, liabilities, expenses,
including reasonable attorneys' fees and cost, which may be incurred by X.
Xxxxx therein or in settlement thereof. Any and all settlements which
restrict the scope or enforceability of Roche Know-How or Roche Patents must
be approved by X. Xxxxx in its sole and absolute discretion before execution
by PDL. Any and all settlements which restrict the scope or enforceability of
Joint Roche-PDL Patents must be approved by X. Xxxxx before execution by PDL,
such approval not to be unreasonably withheld. X. Xxxxx shall not be required
to approve any settlement which does not include as a condition thereof the
granting to X. Xxxxx of a full and unconditional release of claims. X. Xxxxx
will use commercially reasonable efforts to avoid knowingly infringing any
patents of third parties in X. Xxxxx'x design of the cell lines that may be
delivered to PDL hereunder, and X. Xxxxx will inform PDL of any such potential
infringement promptly upon X. Xxxxx'x becoming aware of such potential
infringement.
6A.5 Right to Counsel. Each party to this Amended and Restated
Agreement shall always have the right to be represented by counsel of its own
selection and its own expense in any suit or other action instituted by the
other for infringement, under the terms of this Amended and Restated
Agreement.
6A.6 Coordination. Each party acknowledges and agrees that the efforts
of the parties under this Article VI-A shall take into consideration the
efforts and responsibilities of PDL and Roche under the 1999 PDL/Roche
Agreement.
VII. TERM AND TERMINATION
7.1 Term. Unless earlier terminated pursuant to the terms of this
Article VII, this Amended and Restated Agreement shall remain in effect until
the date of expiration of all payment obligations, including royalties and
reimbursement amounts, under Article III and Article III-A, at which time all
the rights and licenses granted under this Amended and Restated Agreement
shall become irrevocable and fully-paid. Upon the expiration of this Amended
and Restated Agreement pursuant to this Section 7.1, if it is not otherwise
terminated pursuant to this Article VII, (a) in each country in which X. Xxxxx
at the time of expiration has rights to Licensed Products hereunder, PDL shall
grant to X. Xxxxx a nonexclusive, royalty-free license to use the PDL Know-
How, PDL's rights under any Joint Roche-PDL Patents and PDL Patents and cell
lines delivered by PDL pursuant to the 1989 and 1999 PDL/Roche Agreements, but
only to the extent necessary to make, have made, use and sell Licensed
Products for the indications with respect to which X. Xxxxx has rights in
countries in the ROW Territory as of the expiration date; and (b) in each
country in which PDL at the time of expiration retains rights to Daclizumab or
other Licensed Products hereunder, X. Xxxxx hereby grants to PDL a
nonexclusive, fully-paid license under the Roche Patents, Roche Know-How, and
X. Xxxxx'x rights under any Joint Roche-PDL Patents and Joint Inventions but
only to the extent necessary to make, have made, use and sell Daclizumab or
other such Licensed Products in with respect to which PDL has rights in
countries in the ROW Territory as of the expiration date.
7.2 Termination by Mutual Agreement. This Amended and Restated
Agreement may be terminated by the written agreement of the parties.
7.3 Termination by X. Xxxxx. X. Xxxxx may terminate its rights under
this Amended and Restated Agreement upon one hundred eighty (180) days written
notice to PDL.
7.4 Termination by Default.
(a) If either party defaults in the performance of, or fails to be in
compliance with, any material agreement, condition or covenant of this Amended
and Restated Agreement, the party not in default may terminate the other
party's rights this Amended and Restated Agreement at its option; provided,
however, that if such event of default or non-compliance is the first (1st)
occurrence of an event giving rise to the right of termination pursuant to
this Section 7.4, the non-defaulting party may terminate the other party's
rights under this Amended and Restated 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.
(b) If PDL terminates the 1999 PDL/Roche Agreement pursuant to
Section 11.4 thereof, PDL may elect to simultaneously terminate this Amended
and Restated Agreement upon written notice to X. Xxxxx. If Xxxxx terminates
the 1999 PDL/Roche Agreement pursuant to Section 11.4 thereof, X. Xxxxx may
elect to simultaneously terminate this Amended and Restated Agreement upon
written notice to PDL.
7.5 Inventory. Upon termination of this Amended and Restated
Agreement for default by a party hereunder, the defaulting party holding
inventory of Daclizumab shall notify the other of the amount of Daclizumab
such defaulting party, its Affiliates, sublicensees and distributors then have
on hand ("Inventory"), the sale of which would, but for the termination, be
subject to payment of royalties or other consideration under this Amended and
Restated Agreement. The defaulting party and its Affiliates, sublicensees and
distributors shall thereupon be permitted to sell the Inventory, provided that
the other party shall have the first option for a period not to exceed sixty
(60) days to purchase all or part of the Inventory [CONFIDENTIAL TREATMENT
REQUESTED]. If the non-defaulting party fails to exercise its option to
purchase all of the Inventory or for that part of the Inventory with respect
to which the option is not exercised, the party holding the Inventory will be
free to sell such Inventory to third parties for a period not to exceed one
hundred eighty (180) days from the termination of the non-defaulting party's
option. In any event, the parties shall pay the royalties or other
consideration due on the sale of such Inventory in the amounts and manner
provided for in Articles III and III-A. Upon expiration or termination of
this Amended and Restated Agreement for any reason other than default, each of
the parties shall have a right to sell Inventory for a period of one(1) year
from the date of such expiration or termination, subject to the obligation to
pay the royalty or other consideration due to the other party with respect to
the sale of such Inventory. In any event, sales of Inventory by a party
pursuant to this Section 7.5 for Autoimmune Indications shall be in accordance
with the terms and conditions of this Amended and Restated Agreement.
7.6 Return of Materials. Subject to Section 7.8 hereof concerning
archival copies, upon termination of this Amended and Restated Agreement by
X. Xxxxx pursuant to Section 7.3 or by either or both parties pursuant to
Sections 7.2 or 7.4, X. Xxxxx forthwith shall return to PDL all cell lines and
their progeny, antibodies and other biological materials provided by PDL under
the 1989 and 1999 PDL/Roche Agreements.
7.7 Rights and Obligations on Termination or Expiration.
(a) Unless expressly provided to the contrary, the provisions of
Sections 3.6 and 5.3 and Articles III-A, IV, VI-A, VII, VIII, IX and XI shall
survive the termination of this Amended and Restated Agreement. In the event
that termination by either party results in the termination of rights to
Daclizumab or other Licensed Products and the reversion or transfer of such
rights to the other party, then the party whose rights are terminated shall
act in good faith using commercially reasonable efforts to transfer any and
all information, data and materials with the goal of providing minimal
disruption in the marketing and sale of Daclizumab or other Licensed Product,
as the case may be.
(b) In the event of termination (i) by X. Xxxxx pursuant to Section 7.3
or (ii) by PDL for default by X. Xxxxx pursuant to Section 7.4, then effective
as of the date of termination, X. Xxxxx hereby grants to PDL an exclusive,
fully-paid license under the Roche Patents, Roche Know-How, and X. Xxxxx'x
rights under any Joint Roche-PDL Patents and Joint Inventions to make, have
made, use and sell Daclizumab or other such Licensed Products in the ROW
Territory.
7.8 Archival Copies. Section 7.6 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 7.6.
VIII. CONFIDENTIALITY, DISCLOSURE AND PUBLICATIONS
8.1 Confidentiality. During the term of this Amended and Restated
Agreement and for a period of five (5) years following expiration or
termination of this Amended and Restated 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, Roche Know-How, Roche
Patents, Joint Roche-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 Signing 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 Amended and
Restated Agreement or disclose the same to anyone other than those of its
Affiliates, sublicensees, prospective sublicensees, employees, consultants,
agents or subcontractors as are necessary in connection with such party's
activities as contemplated in this Amended and Restated Agreement. Each party
shall be responsible for ensuring compliance with these obligations by such
party's Affiliates, sublicensees, prospective 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.
8.2 Exceptions. The obligation of confidentiality contained in this
Amended and Restated 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 Amended and
Restated 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 Amended and Restated 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.
8.3 Publications.
(a) Scientific Publications. Prior to public disclosure or submission
for publication of a manuscript describing the results of any scientific
activity or collaboration between PDL and X. Xxxxx in the Field, the party
disclosing or submitting such a manuscript ("Disclosing Party") shall send the
other party ("Responding Party") by expedited delivery a copy of the
manuscript to be submitted and shall allow the Responding Party a reasonable
time period (not to exceed forty-five (45) days from the date of confirmed
receipt) in which to determine whether the manuscript contains subject matter
of which patent protection should be sought (prior to publication of such
manuscript) for the purpose of protecting an invention conceived or developed
in connection with the PDL/X. Xxxxx scientific collaboration, or whether the
manuscript contains confidential information belonging to the Responding
Party. After the expiration of forty-five (45) days from the date of
confirmed receipt of such manuscript, the Disclosing Party shall be free to
submit such manuscript for publication and publish or otherwise disclose to
the public such research results. Should the Responding Party believe the
subject matter of the manuscript contains confidential information or a
patentable invention of substantial commercial value to the Responding Party,
then prior to the expiration of forty-five (45) days from the date of
confirmed receipt of such manuscript by the Responding Party, the Responding
Party shall notify the Disclosing Party in writing of its determination that
such manuscript contains such information or subject matter for which patent
protection should be sought. Upon receipt of such written notice from the
Responding Party, the Disclosing Party shall delay public disclosure of such
information or submission of the manuscript for an additional period of sixty
(60) days to permit preparation and filing of a patent application on the
disclosed subject matter. The Disclosing Party shall thereafter be free to
publish or disclose such information, except that the Disclosing Party may not
disclose any confidential information of the Responding Party in violation of
Section 8.1hereof. Determination of authorship for any paper or patent shall
be in accordance with accepted scientific practice. Should any questions on
authorship arise, this will be determined by good faith consultation between
the respective heads of research for each of the parties.
(b) Preclinical and Clinical Studies. Prior to public disclosure or
submission for publication of a manuscript by PDL describing the results of
any preclinical or clinical study conducted by or on behalf of PDL in
Autoimmune Indications, PDL shall send F. Roche by expedited delivery a copy
of the manuscript to be submitted and shall allow F. Roche a reasonable time
period (not to exceed forty-five (45) days from the date of confirmed
receipt by F. Roche) to review the manuscript, including for the purpose of
determining whether the manuscript contains information which is reasonably
likely to have a material adverse impact on Daclizumab for Transplant
Indications in the ROW Territory or confidential information belonging to F.
Roche. After the expiration of forty-five (45) days from the date of
confirmed receipt by F. Roche of such manuscript, PDL shall be free to submit
such manuscript for publication and publish or otherwise disclose to the
public such research results. Should F. Roche believe the manuscript contains
information which is reasonably likely have a material adverse impact on
Daclizumab for Transplant Indications in the ROW Territory or which is
confidential information of F. Roche, then prior to the expiration of forty-
five (45) days from the date of confirmed receipt of such manuscript by F.
Roche, F. Roche shall notify the PDL in writing of its determination and the
reasons therefor. Upon receipt of such written notice from F. Roche that the
manuscript contains confidential information of F. Roche, PDL shall delay
public disclosure of such information or submission of the manuscript for an
additional period not to exceed sixty (60) days to permit the parties to agree
as to how to revise the manuscript so that PDL will not disclose any
confidential information of F. Roche in violation of Section 8.1 hereof.
IX. DISPUTE RESOLUTION
9.1 Arbitration. Except as expressly provided herein, 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 AAA in Santa Clara County, California under
the International Arbitration Rules then in effect for that AAA 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 AAA Administrator in
accordance with the AAA International Rules of Arbitration and the AAA shall
select an individual 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 Amended and Restated 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
10.1 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 courier or overnight dispatch (e.g., Fedex)
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
11.1 Representations of Each Party. Each party represents and warrants
to the other party hereto that, except as may otherwise be disclosed in
writing to such party:
(a) each party has the full right and authority to enter into this
Amended and Restated Agreement; and
(b) to the best knowledge of the party after reasonable investigation,
no third party has any right, title or interest in the PDL
Patents, PDL Know-How, Joint Roche-PDL Patents, Roche Know-How or
Roche Patents, as the case may be, as the result of such third
party's former employment of any employee of that party.
11.2 Assignment. This Amended and Restated Agreement and the licenses
herein granted other than the 1999 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.
11.3 Entire Agreement. This Amended and Restated Agreement and the
1999 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 Amended and Restated Agreement
shall not be changed or modified orally, but only by an instrument in writing
signed by both parties.
11.4 Releases.
(a) The parties agree that as of the Signing Date, PDL hereby releases
and forever discharges F. Roche and its Affiliates (including Genentech, Inc.,
a Delaware corporation) from any and all claims, liabilities and demands
whatsoever on account of or arising from the 1989 F. Roche Agreement that PDL
may have, otherwise continue to have or have had, past, present or future,
including with respect to Article III and Article VII of the 1989 F. Roche
Agreement and including without limitation any and all claims liabilities and
demands on account of or arising from Section 3.1(d) of the 1989 F. Roche
Agreement, including any remedies which PDL may have on, prior to or after the
Signing Date thereunder both in equity and at law; provided that nothing
herein shall be deemed to release any claims, liabilities or demands that PDL
may have after the Signing Date under this Amended and Restated Agreement.
(b) The parties agree that as of the Signing Date, F. Roche and its
Affiliates hereby release and forever discharge PDL from any and all claims,
liabilities and demands whatsoever on account of or arising from that certain
Joint Development, Marketing and License Agreement between PDL and Boehringer
Mannheim GmbH ("Boehringer") dated October 28, 1993, as amended, and all
related agreements entered into between PDL and Boehringer as of that same
date that F. Roche and its Affiliates may have, otherwise continue to have or
have had, past, present or future, including any remedies which Roche may have
on, prior to or after the Signing Date thereunder both in equity and at law;
provided that nothing herein shall be deemed to release any claims,
liabilities or demands that F. Roche or its Affiliates may have after the
Signing Date under this Amended and Restated Agreement.
11.5 Severability. If any provision of this Amended and Restated
Agreement is declared invalid by an arbitrator pursuant to Section 9.1 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 Amended and Restated 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
Amended and Restated 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 Amended and Restated 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 9.1.
11.6 Indemnification.
(a) F. Roche 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
F. Roche, an Affiliate of F. Roche, or any distributor, customer, sublicensee
or representative of F. Roche 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 1999 PDL/Roche Agreement, method, process,
device or apparatus licensed or provided by PDL to F. Roche hereunder, or
(ii) as a result of practicing a Joint Invention, or using PDL Know-How or PDL
Patents licensed to F. Roche under this Amended and Restated Agreement, except
where such claim is based on the negligent acts of commission or omission of
PDL.
(b) PDL shall defend, indemnify and hold harmless F. Roche, 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 PDL, an
Affiliate of PDL, or any distributor, customer, sublicensee or representative
of PDL or anyone in privity therewith, of Daclizumab or any other Licensed
Product in Autoimmune Indications, or (ii) as a result of practicing a Joint
Invention, using Roche Know-How or Roche Patents licensed to PDL under this
Amended and Restated Agreement, except where such claim is based on the
negligent acts of commission or omission of F. Roche.
11.7 Notices. Any notice or report required or permitted to be given
under this Amended and Restated 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.
34801 Campus Drive
Fremont, California U.S.A. 94555
Attention: General Counsel
If to F. Roche: F. Hoffmann-La Roche Ltd
Grenzacherstrasse 124
CH-4002 Basle, Switzerland
Attention: Law Department
11.8 Choice of Law. The validity, performance, construction, and
effect of this Amended and Restated Agreement shall be governed by the laws of
the State of California, United States of America.
11.9 Publicity. Both parties agree to issue a press release concerning
entry into this Amended and Restated Agreement, with the content of such
release 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 Amended and
Restated 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.
Notwithstanding anything to the contrary herein, if not otherwise disclosed by
F. Roche, PDL shall not disclose to any third party the amount of sales of or
royalties or consideration paid with respect to Licensed Product without the
prior written consent of F. Roche, which consent shall not be unreasonably
withheld.
11.10 Headings. The captions used herein are inserted for convenience
of reference only and shall not be construed to create obligations, benefits,
or limitations.
[The remainder of this page intentionally left blank.]
11.11 Counterparts. This Amended and Restated 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 Amended and Restated
Agreement to be effective as of the Signing Date.
PROTEIN DESIGN LABS, INC.
By
Title:
Date:
F. HOFFMANN-LA ROCHE LTD
By
Title:
Date:
Solely with respect to the granting of rights in Joint Roche-PDL Patents to F.
Roche, Roche hereby joins in this Amended and Restated Agreement.
HOFFMANN-LA ROCHE INC.
By
Title:
Date:
Appendix A
PDL Patents
A. The following are patents and patent applications (also known as the "Queen
et al. Patents") issued and filed in certain countries in the world.
1. The following issued U.S. patents and U.S. patent applications:
No. 5,585,089, "Humanized Immunoglobulins," issued December 17, 1996.
No. 5,693,761, "Polynucleotides Encoding Improved Humanized
Immunoglobulins," issued December 2, 1997.
No. 5,693,762, "Humanized Immunoglobulins," issued December 2, 1997.
[CONFIDENTIAL TREATMENT REQUESTED]
2. The following patents and patent applications outside the U.S.:
Patent No.
Country
Title*
Issued
647383
Australia
"Novel Immunoglobulins, Their Production
and Use"
Issued
671949
Australia
"
Issued
AT E133452
Austria
"
Issued
0451216
Belgium
"
Issued
61095
Bulgaria
"
Issued
970016
Brazil
"
Issued
0451 216B1
European
"
Issued
0682040 B1
European
Issued
FR0451216
France
"
Issued
DE
68925536
Germany
"
Issued
DD 296 964
East Germany
"
Issued
GB 0451216
Great Britain
"
Issued
1001050
Greece
"
Issued
211174
Hungary
"
Issued
IT O451216
Italy
"
Issued
2828340
Japan
"
Issued
LU O451216
Luxembourg
"
Issued
92.2146
Monaco
"
Issued
NL 0451216
Netherlands
"
Issued
231984
New Zealand
"
Issued
132068
Pakistan
"
Issued
29729
Philippines
"
Issued
92758
Portugal
"
Issued
4895847.13
Russia
"
Issued
2126046
Russia
"
Issued
SG O451216
Singapore
"
Issued
89/9956
South Africa
"
Issued
178385
South Korea
"
Issued
2081974 T3
Spain
"
Issued
SE O451216
Sweden
"
Issued
CHO 451216
Switzerland
"
Issued
50034
Taiwan
"
Issued
13349
Uruguay
"
Issued
48700
Yugoslavia
"
Country
Title*
Pending
Argentina
"Novel Immunoglobulins, Their
Production and Use"
Pending
Canada
"
Pending
Chile
"
Pending
China
"
Pending
Croatia
"
Pending
Czech Republic
"
Pending
Ecuador
"
Pending
Europe
"
Pending
Hong Kong
"
Pending
Ireland
"
Pending
Israel
"
Pending
Japan
"
Pending
South Korea
Pending
Romania
"
Pending
Slovak Republic
"
Pending
Venezuela
"
Pending
Denmark
"
Pending
Finland
"
Pending
Norway
"
*Exact titles may differ in different countries.
B. The following patent applications relate to the use of anti-IL2 receptor
antibodies in treatment of acute transplant rejection.
Title: Method of preventing acute rejection following solid organ
transplantation.
Inventors: Susan Light and Cary Queen
PCT Publication No.: WO 98/13067 claiming priority to U.S. provisional
patent application serial no. 60/026,643 filed September 24, 1996.
(footnote continued from previous page)
(footnote continued on next page)
common/contracts/roche//Roche 99ROW Amend 8.0
--
CONFIDENTIAL TREATMENT REQUESTED WITH RESPECT TO
DESIGNATED PORTIONS OF THIS DOCUMENT
common/contracts/roche//Roche 99 ROWAmend v8.0
