1
EXHIBIT 10.55
Confidential Materials omitted and filed
separately with the Securities and Exchange
Commission. Asterisks denote omissions.
AMENDMENT NO. 1 TO
COLLABORATIVE RESEARCH AGREEMENT AND
LICENSE OPTION, LICENSE AND ROYALTY AGREEMENT
EACH DATED AS OF JANUARY 1, 1995
This Agreement dated as of December 1998 by and between Pfizer Inc, a Delaware
corporation having an office at 000 Xxxx 00xx Xxxxxx, Xxx Xxxx, Xxx Xxxx 00000
(together with its Affiliates, "Pfizer") and Millennium Pharmaceuticals, Inc., a
Delaware corporation having an office at 000 Xxxx Xxxxxx, Xxxxxxxxx,
Xxxxxxxxxxxxx 00000 (together with its Affiliates, "Millennium").
Whereas, Pfizer and Myco Pharmaceuticals, Inc. ("Myco") entered into a
Collaborative Research Agreement dated as of January 1, 1995 (the "Research
Agreement") and a License Option, License and Royalty Agreement dated as of
January 1, 1995 (the "License Agreement" and together with the Research
Agreement, the "1995 Agreements"); and
Whereas, Millennium is the successor in interest to Myco under the 1995
Agreements; and
Whereas, Pfizer and Millennium wish to extend the Research Program under
the Research Agreement, modify the scope of the research and other licenses
thereunder and under the License Agreement, and amend certain other provisions
of the 1995 Agreements;
NOW THEREFORE, the parties agree as follows:
1. Amendments to the Research Agreement
1.1 The term "Millennium" shall replace the term "Myco" wherever the
latter appears in the Research Agreement.
1.2 Section 1 is hereby amended by adding the phrase", subject to such
written amendment as the parties, acting through the Research Committee, may
adopt from time to time," at the end of the existing text of Section 1.9 and by
deleting
-1-
2
Confidential Materials omitted and filed
separately with the Securities and Exchange
Commission. Asterisks denote omissions.
the existing definitions after Section 1.18 and adding the following new
definitions after the text of Section 1.18:
"1.19 `Patent Rights" shall mean the issued patents and pending
applications, whether domestic or foreign, claiming all inventions within
Program Technology and all inventions made by Pfizer using Program Technology
during the Exclusivity Period including all continuations,
continuations-in-part, division and renewals, all letters patent granted
thereon, and all reissues, reexaminations and extensions thereof."
"1.20 `Product' means an Antifungal Drug the manufacture, use, sale,
offer for sale or importation of which in the absence of a license would
infringe a claim within Patent Rights."
"1.21 `Cost/person year' means, in the first four Commitment Years of
the Contract Period, [**]; and, in the fifth and sixth Commitment Years of the
Contract Period, [**]
"1.22 `Program Technology' means, collectively, Millennium Program
Technology, Pfizer Program Technology and Joint Technology."
"1.23 `Program Materials' means any biological, synthetic chemical and
biochemical materials that are part of Program Technology."
"1.24 `Target' means any Program Technology consisting of any gene or
protein encoded by such gene which in the course of the Research Program is
identified as a potentially useful target for the identification or development
of Antifungal Drugs."
"l.25 `[**]' means the [**]."
"1.26 `[**]' means any Product acting at the [**]."
"1.27 `Exclusivity Period' means the period beginning January 1, 1999
and ending on the first to occur of (a) the third anniversary of the conclusion
of the Contract Period or (b) the second anniversary of the conclusion of the
Contract Period if, before such anniversary, Millennium has notified Pfizer that
Millennium is exercising its option to shorten such period so that it ends on
said second anniversary."
"1.28 `Candidate Product' means a compound (a) which Pfizer identifies
in the course of the Research Program or the Exclusivity Period, and (b) which
Pfizer believes satisfies (1) a Profile of Activity and (2) an appropriate
safety profile and (c) which Pfizer believes is a bona fide candidate for
development as an Antifungal Drug."
"1.29 `Lead' means a compound (a) which is identified in a screen
employing a Target and (b) which Pfizer selects to begin structural modification
to yield a Candidate Product."
-2-
3
Confidential Materials omitted and filed
separately with the Securities and Exchange
Commission. Asterisks denote omissions.
1.3 The membership of the Research Committee, as provided by Section 2.2,
is hereby amended to be as follows:
Pfizer Appointees: [**]
[**]
[**]
Millennium Appointees: [**]
[**]
[**]
1.4 Section 3.1 is hereby amended and restated in its entirety to read as
follows:
"3.1 The Annual Commitment for each Commitment Year is as follows:
Commitment Year Annual Commitment
[**] [**]
[**] [**]
[**] [**]
[**] [**]
[**] [**]
[**] [**]"
1.5 Section 4.1.1 is hereby amended and restated in its entirety to read
as follows:
"4.1.1 Pfizer and Millennium each recognize that the other's
Confidential Information constitutes highly valuable confidential information.
Subject to the terms and conditions of the License Option, License and Royalty
Agreement of even date with this Agreement (the "License Agreement"), the
obligations set forth in Section 4.3 and the publication rights set forth in
Section 4.2, Pfizer and Millennium each agree that during the term of this
Agreement and during the Exclusivity Period, it will keep confidential, and will
cause its Affiliates to keep confidential, all Millennium Confidential
Information or Pfizer Confidential Information, as the case may be, that is
disclosed to it or to any of its Affiliates under this Agreement. Neither Pfizer
nor Millennium or any of their respective Affiliates shall use such Confidential
Information of the other party except as expressly permitted in this Agreement
or the License Agreement."
-3-
4
Confidential Materials omitted and filed
separately with the Securities and Exchange
Commission. Asterisks denote omissions.
1.6 Section 4.5 is hereby amended and restated in its entirety to read as
follows:
"4.5 RESTRICTIONS ON TRANSFERRING PROGRAM MATERIALS. Pfizer and Millennium
recognize that Program Materials represent valuable commercial assets. During
the Exclusivity Period, neither party shall transfer to a third party any
Program Materials, unless such transfer is (1) first approved in writing by the
other party or (2) otherwise expressly permitted by this Agreement or the
License Agreement; provided that the foregoing restriction shall not apply to
Pfizer Non-Program Technology in the case of Pfizer or to Millennium Non-Program
Technology (including improvements to Millennium Non-Program Technology made in
the course of the Research Program) in the case of Millennium."
1.7 Section 5.2 is hereby amended and restated to read in its entirety as
follows:
"5.2 GRANTS OF RESEARCH LICENSES. (a) Millennium and Pfizer each hereby
grants to the other a nonexclusive, irrevocable, worldwide, royalty-free,
perpetual license, including the right to grant sublicenses to Affiliates to
make and use Confidential Information, Program Technology and Patent Rights for
all research purposes.
(b) During the exclusivity Period, Pfizer shall have the exclusive
right to seek Products based on the Program Technology.
(c) Notwithstanding the provisions of Subsection 5.2(b), if during
the exclusivity Period Pfizer withdraws its medicinal chemistry program
associated with the [**], Pfizer shall so notify Millennium in writing and
Millennium shall then have the right, exercisable within 90 days of such notice,
to obtain from Pfizer (1) an exclusive royalty-fee research license for the [**]
to discover Products (the "NMT Research License"); (2) subject to Pfizer's
exclusive reservation set forth in Section 2.2 of the License Agreement, an
exclusive, royalty-bearing, worldwide license to make, use, sell, offer for sale
and import Products discovered using the NMT Research License (the "NMT
Commercial License"); (3) copies of, and the right to use under the NMT Research
License, Pfizer Confidential Information relating to the NMT program and (4) up
to six different samples, each of 50 milligrams, selected by Millennium from
among the analogues prepared by Pfizer in the course of its medicinal chemistry
program associated with the [**], to the extent such samples are then available.
Pfizer shall be under no obligation to re-synthesize any compounds in order to
provide Millennium with such samples."
-4-
5
Confidential Materials omitted and filed
separately with the Securities and Exchange
Commission. Asterisks denote omissions.
1.8 Section 5.4 is hereby amended to add the following phrase before the
first sentence of the existing text "Subject to the obligations to pay royalties
on products set forth in Section 3.2 of the License Agreement". Further,
Section 5.4 is hereby amended so that the term "Program Technology" replaces the
term "Joint Technology" wherever the latter appears, and so that the term
"Patent Rights" replaces the term "Joint Patent Rights" wherever the latter
appears.
1.9 Section 9.1 is hereby amended so that the term "December 31, 2000"
replaces the term "December 31, 1998."
2. Amendments to the License Agreement
2.1 The term "Millennium" shall replace the term "Myco" wherever the
latter appears in the License Agreement.
2.2 Sections 2.1 and 2.2 are amended and restated to read in their
entirety as follows:
"2.1 Licenses Under the Patent Rights.
(a) Subject to the provisions of Section 2.1(c) below, Millennium
hereby grants Pfizer an exclusive license ("License"), including the right to
grant sublicenses, under the Patent Rights to make, use, sell, offer for sale
and import any Product for human pharmaceutical purposes.
(b) Subject to the provisions of Section 5.2(b) of the Research
Agreement, Pfizer hereby grants Millennium an exclusive license, including the
right to grant sublicenses, under the Patent Rights to make, use, sell, offer
for sale and import Program Technology for research purposes [**] after the end
of the Exclusivity Period.
(c) Whenever Pfizer, in the course of the Research Program or during
the Exclusivity Period, identifies a Candidate Product, then Pfizer shall so
notify Millennium and issue a "Candidate Alert Notice" or equivalent in
accordance with Pfizer's internal procedures. Pfizer shall then have [**] in
which to determine whether to pursue the development of such Candidate Product.
If Pfizer determines to pursue the development of such Candidate Product, it
will be treated as a Product under Section 2.1(a) above. If Pfizer does not
pursue the development of such Candidate Product, Pfizer shall nevertheless have
the right to reconsider such Candidate Product during the [**] period following
its decision not to pursue its
-5-
6
Confidential Materials omitted and filed
separately with the Securities and Exchange
Commission. Asterisks denote omissions.
development. If Pfizer does not pursue the development of such Candidate Product
during such time period, Millennium will be free to develop and commercialize
such Candidate Product itself or with third parties after the expiration of such
[**] time period, provided however that Millennium shall not have such right if
(1) Pfizer discontinues development of such Candidate Product because of
Pfizer's determination, in its sole unfettered discretion, that the Candidate
Product is unsafe or (2) Pfizer is developing or selling a Product with the same
Profile of Activity. If Millennium commercializes such Candidate Product,
Millennium shall be obligated to pay Pfizer a royalty with respect to commercial
sales of such Product, as set forth in Section 3.10 hereof. In such
circumstances, Pfizer shall have no rights to such Candidate Product or any
resulting Product.
2.2 OPTION EXERCISE BY PFIZER AS TO POTENTIAL [**] IDENTIFIED BY
MILLENNIUM.
(a) Millennium hereby grants Pfizer the option to acquire an
exclusive, worldwide, royalty-bearing license to commercialize any [**] arising
under an NMT Research License obtained by Millennium under Section 5.2(c) of the
Research Agreement.
(b) If Millennium identifies any potential [**] arising under an NMT
Research License and if Millennium thereupon decides, using a format
substantially similar to a Candidate Product, to nominate such potential [**]
for development, Millennium will notify Pfizer within [**] of such decision and
will supply Pfizer, as Pfizer may request before or after such notification,
with all Millennium Confidential Information relating to such potential [**].
Pfizer shall have a period of [**] following such notification in which to
exercise the option as to that potential [**]."
2.3 Section 2.3 is hereby amended to read in its entirety as follows:
"Unless terminated earlier as provided below, the licenses granted
hereunder shall terminate on the date of the last to expire of the Patent
Rights."
2.4 Section 3.1 is hereby amended by renumbering and recaptioning "3.1
Payment of Royalties" as "3.1(a) Payment of Royalties by Pfizer" and adding,
after the end of the existing text, the following text;
"3.1(b) PAYMENT OF ROYALTIES BY MILLENNIUM.
During the term of any license granted by Pfizer to Millennium to
commercialize any [**] pursuant to Section 5.2(c) of the Research Agreement,
Millennium shall pay Pfizer a royalty equal to [**] of the Net Sales of such
[**]. Such
-6-
7
Confidential Materials omitted and filed
separately with the Securities and Exchange
Commission. Asterisks denote omissions.
royalties shall be determined and paid in the same manner as Pfizer would be
required by the terms of this Agreement to determine and pay royalties."
2.5 Section 3.2.3 is hereby amended and restated to read in its entirety
as follows:
"3.2.3 (a) The royalty paid by Pfizer to Millennium for any (i) Product or
(ii) therapeutic or prophylactic product for human pharmaceutical use made under
the licenses granted in Section 5.4 of the Research Agreement, in each case for
which Pfizer identifies a Lead during the Exclusivity Period, shall be the sum
of the Net Sales in each Tier multiplied by the applicable royalty rate for that
Tier as follows:
Minimum Royalty Rates
Net Sales in Millions of Royalty Rates as a as a Percentage of Net
Dollars ("Tiers") Percentage of Net Sales Sales
-------------------------- -------------------------- -------------------------
[**] [**] [**]
[**] [**] [**]
[**] [**] [**]
[**] [**] [**]
[**] [**] [**]
Except for the deduction permitted by Section 3.2.4 and the credit permitted by
Section 3.8, the Minimum Royalty Rate in the third column above is the absolute
minimum after all offsets and deductions permitted under this Agreement.
(b) The royalty paid by Pfizer to Millennium for any (i) Product or (ii)
therapeutic or prophylactic product for human pharmaceutical use made under the
licenses granted in Section 5.4 of the Research Agreement, in each case for
which Pfizer identifies a Lead after the Exclusivity Period shall be 5% of the
Net Sales of such Product or such product."
2.6 Section 3.2 is hereby further amended by adding, after Subsection
3.2.3, a new Subsection 3.2.4 reading as follows:
"3.2.4 (a) If Millennium or any Millennium sublicensee develops and sells a
Product that acts at the same Target as a Product sold by Pfizer, Pfizer's
royalty obligations to Millennium under Section 3.2.3 shall be calculated on a
country-by-country basis using a percentage equal to [**] of the relevant
percentage
-7-
8
Confidential Materials omitted and filed
separately with the Securities and Exchange
Commission. Asterisks denote omissions.
shown in Section 3.2.3 for any country in which Millennium or any Millennium
sublicensee sells such product."
2.7 Section 3.6 is hereby amended to add, at the end of the first sentence
of the existing text, the following phrase;
", for a period ending with the expiration of the last European or United
States patent covering such Product."
2.8 Section 3.8 is hereby amended by renumbering and recaptioning the
existing text as "3.8.1 Milestones -- General" and by adding the phrase "Except
as provided in Subsection 3.8.2" before the existing text and by adding, after
the existing text, a new Subsection 3.8.2 reading as follows;
"3.8.2 Milestones -- [**]
If Pfizer exercises its option pursuant to Section 2.1 (a)(ii) to license
from Millennium the rights to make, use and sell a [**] developed by Millennium,
then the payments otherwise required under Subsection 3.8.1 for such Product
shall as set forth below:
EVENT AMOUNT
[**] [**] [**]
[**] [**] [**]
[**] [**] [**]
[**] [**] [**]
[**] [**] [**]
2.9 Section 10 is hereby amended to insert the following new Section 10.3
and 10.4 after the text of existing Section 10.2:
"10.3 Indemnification of Pfizer by Millennium
Millennium shall indemnify, defend and hold harmless Pfizer and its
directors, officers, employees, and agents and their respective successors,
heirs and assigns (the "Pfizer Indemnitees"), against any liability, damage,
loss or expense (including reasonable attorneys' fees and expenses of
litigation) incurred by or imposed upon
-8-
9
Confidential Materials omitted and filed
separately with the Securities and Exchange
Commission. Asterisks denote omissions.
the Pfizer Indemnitees, or any one of them, in connection with any claims,
suits, actions, demands or judgments, including without limitation personal
injury and product liability matters (except in cases where such claims, suits,
actions, demands or judgments result from the material breach, negligence or
willful misconduct on the part of Pfizer), arising out of the production,
manufacture, promotion, sale or use by any person of any Product or Antifungal
Drug which is manufactured or sold by Millennium or by an Affiliate,
sublicensee, distributor or agent of Millennium.
10.4 The indemnification set forth in Section 10.3 shall not apply if a
Pfizer Indemnitee fails to give Millennium prompt notice of any claim it
receives and such failure materially prejudices Millennium with respect to any
claim or action to which Millennium's obligation pursuant to this Section
applies. Millennium, in its sole discretion, shall choose legal counsel, shall
control the defense of such claim or action, and shall have the right to settle
same on such terms and conditions as it deems advisable."
3. Other Matters
Except as expressly provided herein, all of the terms and provisions of the
Agreements remain in full force and effect.
In Witness Whereof, the parties have caused their respective authorized
representatives to execute and deliver counterparts of this Amendment No. 1.
Pfizer Inc
By /s/ Xxxxxx X. Xxxxx, Xx.
-------------------------------
(Signature)
Xxxxxx X. Xxxxx, Xx., Vice President
------------------------------------
Name and Title (Print)
Millennium Pharmaceuticals, Inc.
By /s/ Xxxx X. Xxxxx
-------------------------------
(Signature)
Xxxx X. Xxxxx, President and CEO
------------------------------------
Name and Title (Print)
-9-
