Exhibit 10.16
LICENSE AND CLINICAL TRIALS AGREEMENT
Agreement ("AGREEMENT"), effective as of February 27, 1995 ("Effective
Date") between VIRUS RESEARCH INSTITUTE, INC., a Delaware corporation, with its
principal place of business at 00 Xxxxxxx Xxxxxx, Xxxxxxxxx, Xxxxxxxxxxxxx 00000
(hereinafter referred to as "VRI") and the XXXXX X. XXXXXX INSTITUTE OF MEDICAL
RESEARCH, an Ohio non-profit corporation, with its principal place of business
at 0000 Xxxxxx Xxxxxx, Xxxxxxxxxx, Xxxx 00000 (hereinafter referred to as
"XXXXXX").
WITNESSETH:
WHEREAS, XXXXXX is the owner of certain rights in technology as defined
herein; and
WHEREAS, XXXXXX desires to have such rights utilized to promote the public
interest by granting a license thereunder;
WHEREAS, VRI is engaged in the development, production, marketing and sale
of products similar to the technology which is the subject of this AGREEMENT and
has the strategic commitment to facilitate the transfer of such technology for
the public interest; and
WHEREAS, VRI desires to obtain a license to said rights upon the terms and
conditions hereinafter set forth;
WHEREAS, VRI desires to utilize XXXXXX'x services with respect to the
conduct of certain of the clinical trials and laboratory services needed to
obtain FDA approval for XXXXXX'X rotavirus vaccines.
NOW THEREFORE, in consideration of the mutual covenants herein contained
and intending to be legally bound hereby, the parties hereto agree as follows:
1. DEFINITIONS.
1.1 "Invention(s)" shall mean rotavirus vaccines, developed from rotavirus
strain 89-12, including that which was safety tested by Xxx Xxxxxx, Ph.D. of
PRI/DynCorp for XXXXXX and received by XXXXXX on 12/2/93 or modification of
rotavirus strain 89-12 generated by natural or site-directed mutagenesis, that
stimulate neutralizing antibody to multiple serotypes of human rotavirus, and
methods for vaccinating humans against rotavirus illness caused by rotaviruses
of different serotypes using rotavirus strain 89-12 and for expanding the titers
and memory of the cells that express the pre-existing neutralizing antibodies
induced following primary vaccination against rotavirus disease using solely
rotavirus strain 89-12. The Invention(s) include inactivated vaccines using
rotavirus strain 89-12.
1.2 "Technical Information" shall mean vaccine production information and
the results of the safety and identity testing conducted by Xxx Xxxxxx, Ph.D.,
of PRI/DynCorp and received by XXXXXX on 12/2/93 and information regarding the
history, culture, adaptation and attenuation of rotavirus strain 89-12; and
scientific, technical and medical information related to 89-12, generated by or
on behalf of XXXXXX or obtained from Xx. Xxxxxx as part of the quality assurance
process during the term of this AGREEMENT.
1.3 "Patent Rights" shall mean any current or fixture United States or
foreign patent applications which are set forth in Appendix A attached hereto
and arising from Inventions owned by or assigned to XXXXXX, together with any
divisions and continuations (related to rotavirus strain 89-12)
continuations-in-part (related solely to rotavirus strain 89-12 and improvements
thereto), patents issuing
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thereon and reissues thereof and extensions thereof; provided that in the case
of future patent applications and patents, inclusion in Patent Rights shall be
subject to reimbursement by VRI to XXXXXX of the cost of Research and
Development with respect thereto. Nothing in this Agreement gives VRI rights to
Improvements in a vaccine which does not employ rotavirus strain 89-12.
1.4 "Licensed Products" shall mean any product which is covered in whole
or in part by a Valid Claim in the Patent Rights and/or which incorporates or
utilizes to a significant degree Technical Information.
1.5 "Licensed Process" shall mean any process which is covered in whole or
in part by a Valid Claim in the Patent Rights and/or which incorporates or
utilizes to a significant degree Technical Information.
1.6 "Territory" shall mean the entire world.
1.7 "Net Sales" shall mean the gross revenue received by VRI, its
Affiliates from the sales of Licensed Products or Licensed Processes to
independent third parties less:
(a) Transportation charges or allowances separately stated and
invoiced;
(b) Trade, quantity, cash, rebates or other allowances and discounts
and brokers', distributors', or agents' commissions actually allowed and taken;
(c) Credits or allowances made or given on account of rejects or
returns;
(d) Medicare and Medicaid disallowed reimbursements;
(e) Taxes levied on and/or other governmental charges made as to
production, sale, transportation, delivery or use and paid by or on behalf of
Licensee.
Licensed Products shall be considered "sold" when invoiced.
1.8 "Sublicensee" shall mean any corporation, partnership or business
organization which is not an Affiliate to which VRI grants a license to enable
said party to sell Licensed Products or utilize Licensed Processes.
1.9 "Affiliate" shall mean any corporation or other business entity
controlled by, controlling, or under common control with VRI. For this purpose
"control" means direct or indirect beneficial ownership of at least fifty
percent (50%) interest in the income or stock of such corporation or other
business.
1.10 "Valid Claim" shall mean a claim of an issued patent or pending
patent application which has not been pending for more than five (5) years from
the relevant U.S. priority date, January 3, 1992, which has not lapsed or become
abandoned or been declared invalid or unenforceable by a court of competent
jurisdiction or an administrative agency from which no appeal can be or is
taken.
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2. GRANT
2.1 XXXXXX hereby grants to VRI the exclusive right and license under
Patent Rights and Technical Information to make, have made, use, lease, have
leased, sell, and have sold the Licensed Products and to practice the Licensed
Processes in the Territory for the term of this AGREEMENT unless this AGREEMENT
is sooner terminated according to the terms hereof. VRI shall have the right to
extend the grant set forth in this Section 2.1 to its Affiliates.
2.2 Notwithstanding the provision of Section 2.1, XXXXXX shall retain the
right to make, use and practice the Invention(s) and the Technical Information
for its own non-commercial, research purposes. XXXXXX shall have the right to
convey to other non-profit organizations at no charge other than shipping fees,
the Invention(s) and Technical Information for use in non-commercial, basic
research, provided that such organizations have entered into agreements in
substantially the form attached as Appendix B.
2.3 VRI agrees that any Licensed Products subject to obligations under
Public Laws 96-517 or 98-620 and which are intended for sale in the United
States shall be manufactured substantially in the United States. In the event
that VRI determines that compliance with the foregoing obligation is
commercially impracticable, XXXXXX agrees that it will cooperate with VRI in
attempting to obtain from the U.S. Government a waiver of such obligation.
2.4 (a) VRI will have the right, subject to the terms of this AGREEMENT,
to enter into sublicensing agreements with any other entity (other than an
Affiliate to whom the license may be extended in accordance with Section 2.1)
for the rights, privileges and licenses granted hereunder.
(b) VRI agrees that any sublicenses granted by it shall provide that
the obligations to XXXXXX contained in the following provisions of this
AGREEMENT shall be binding upon the Sublicensee: Sections 2.4 (c), 8 and 10. VRI
further agrees to attach a copies of such provisions to each sublicense
agreement.
(c) VRI agrees to forward to XXXXXX a copy of any and all fully
executed sublicense agreements within thirty (30) days of execution thereof, and
further agrees to forward to XXXXXX annually a copy of such reports received by
VRI from its Sublicensee during the preceding twelve (12) month period under the
sublicenses as shall be pertinent to a royalty accounting under said sublicense
agreements. VRI may delete from copies of sublicense agreements provided to
XXXXXX hereunder commercial, research and development, manufacturing, financial
and other provisions unrelated to VRI's or the Sublicensee's obligations to
XXXXXX.
(d) In the event that this AGREEMENT is terminated prior to its
normal expiration, any sublicense granted by VRI shall remain in full force and
effect from and after that date as a direct license between XXXXXX and the
Sublicensee, to the extent that the royalty obligations of VRI in individual
countries have not ceased pursuant to the terms of this AGREEMENT and the
Sublicensee's agreement to be bound by the terms and conditions set forth in
this AGREEMENT.
2.5 (a) In addition to the license granted herein, XXXXXX grants to VRI an
exclusive option to obtain a world-wide, exclusive royalty-bearing license to
any improvement(s) on the Invention(s) that (i) are not subject to prior
commitments to other parties; (ii) relate to the diagnosis, treatment and/or
prevention of human rotavirus illnesses employing strain 89-12; (iii) which are
not specifically included in the Invention(s) or Patent Rights; and (iv) provide
a significant commercial advantage, herein collectively ("Improvements").
(b) Such option shall extend for a period of sixty (60) days from
the date VRI receives written notice from XXXXXX disclosing such Improvement.
During such sixty (60) day period,
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XXXXXX shall reasonably make available to VRI any other information in its
possession or control which would be useful to VRI in evaluating the
improvement. In the event VRI decides to exercise its option, VRI shall do so by
notifying XXXXXX in writing during such sixty (60) day period. Upon exercise of
VRI's option, XXXXXX and VRI shall enter into a license agreement containing
substantially the same provisions as the applicable provisions of this AGREEMENT
except for the initial license fee which shall be at least an amount sufficient
to reimburse XXXXXX for its costs relating to the development of the
Improvement, plus XXXXXX'x actual patent costs relating thereto.
(c) The written notice to XXXXXX of VRI's exercise of its option
hereunder shall include instructions to XXXXXX as to whether VRI wishes XXXXXX
to have a patent application prepared and filed with respect to any such
improvement VRI shall pay for all patent costs relating to any Improvement to
which VRI exercises its option.
(d) In the event that VRI does not exercise its option hereunder or
if the parties have not entered into a license agreement as described in Section
2.5 (b)(1) above at the close of sixty (60) days from VRI's notice of exercise,
XXXXXX shall be free to offer a license for the Improvement on terms of its own
choosing to a third party, provided the terms are not more favorable than those
terms offered to VRI. VRI will grant a sublicense under Patent Rights to such
third party, if required, royalty-free, to permit such party to develop and sell
such Improvement.
2.6 As soon as reasonably possible following the Effective Date of this
AGREEMENT, but in no event later than thirty (30) days alter the Effective Date,
XXXXXX shall provide to VRI copies of all Technical Information directly
relating to the Invention(s) in its possession and control on the Effective
Date. In addition, XXXXXX shall transfer to VRI all supplies of rotavirus strain
89-12 and the master and working cellbanks except as may be necessary for XXXXXX
to conduct such basic research as may be agreed upon by the parties. Upon
termination of this AGREEMENT, as a result of a breach by VRI or by VRI pursuant
to Section 7.4, VRI shall return all Technical Information to XXXXXX.
3. CLINICAL TRIALS AND DUE DILIGENCE
3.1 (a) XXXXXX and VRI will cooperate with one another to complete all
pre-clinical studies necessary for the continued support of the Investigational
New Drug application ("IND") filed with the U.S. Food and Drug Administration
(FDA) and for foreign equivalents filed with respect to a Licensed Product. VRI
shall consult with XXXXXX, shall provide XXXXXX with drafts of the regulatory
submission prior to its filing, and shall not unreasonably refuse to comply with
any request by XXXXXX for any changes thereto, but all regulatory filings shall
be submitted in the name of VRI and VRI shall have the final authority with
respect to their content. XXXXXX shall cooperate with VRI in responding to any
comments of the FDA with respect to its regulatory filing.
(b) Following approval under FDA regulations that clinical trials
may commence under the IND for which approval has been granted, XXXXXX,
recognizing the need for expeditious handling of all matters for which XXXXXX is
responsible herein, agrees that XXXXXX will use reasonable efforts to promptly
conduct the clinical trials and necessary laboratory work provided for in the
IND, subject to the following:
(1) In consultation with and subject to the approval of VRI,
XXXXXX will use reasonable efforts to design and draft the protocols with
respect to Phase I clinical trials;
(2) In consultation with, and subject to the approval of VRI,
XXXXXX will use reasonable efforts to design and draft the protocols with
respect to Phase II clinical trials;
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(3) XXXXXX will use reasonable efforts to conduct the initial
Phase II clinical trials and, subject to consultation with and the approval of
VRI, conduct and/or participate in confirmatory or other Phase II clinical
trials, together with all laboratory work; as required;
(4) if other sites are required in connection with Phase II
clinical trials, VRI will consult with XXXXXX regarding the use and selection of
other sites and XXXXXX will use reasonable efforts to assist VRI in selecting
such additional sites;
(5) XXXXXX and VRI will use reasonable efforts to jointly
design and draft protocols for Phase III clinical trials and XXXXXX may, at
XXXXXX'x option, participate as one of multiple centers for the clinical trials;
Dependent upon FDA requirements, XXXXXX will use reasonable efforts to conduct
all laboratory work required therefore; provided, however, that if XXXXXX'x
laboratory capabilities are not sufficient for the central lab work required for
Phase III clinical trials, XXXXXX will use reasonable efforts to assist VRI in
selecting and approving an appropriate central laboratory and will use
reasonable efforts to supervise that laboratory in its performance of such work;
(6) promptly after completion of the above-described clinical
trials, XXXXXX will cooperate with VRI in preparation and submission to the FDA
of an appropriate application for approval with respect to the Licensed Product
(PLA/NDA) and in the submission of regulatory filings in foreign countries;
(7) if the PLA/NDA is not approved, XXXXXX will cooperate with
VRI at VRI's expense in taking any further action required to obtain its
approval;
(8) XXXXXX will use reasonable efforts to conduct all trials
with the prior approval and ongoing review of all appropriate and necessary
review authorities and in accordance with applicable federal, state and local
laws and regulations and will provide VRI with written evidence of review and
approval of each trial by the appropriate Institutional Review Board prior to
the initiation of each trial and of that Board's continuing review and approval
of each trial whenever it is reviewed, but at least once per year;
(9) XXXXXX will furnish VRI with the data resulting from the
clinical trials within a reasonable time alter completion of each trial,
provided that XXXXXX will permit representatives of VRI to examine XXXXXX'x
facilities, validate case reports against original data in its files and monitor
work performed, at reasonable times and in a reasonable manner at mutually
agreed upon times during the term of this AGREEMENT, to determine the adequacy
of the facilities and whether the clinical trials are being conducted in
compliance with the protocol and relevant FDA regulations;
(10) XXXXXX will retain original records of the clinical
trials conducted by XXXXXX including the original of all volunteer consent forms
in strict accordance with all federal regulations.
(11) XXXXXX shall compile clinical trial data and provide
copies of the complete data set to VRI in a timely manner. XXXXXX will cooperate
with VRI in the analysis of the clinical data.
(12) XXXXXX is conducting the adult and child phases of the
Phase I clinical trials described in the protocols entitled "Reactivity and
Immunogenicity of Live, Attenuated Rotavirus Vaccine Candidate Strain 89-12."
and attached as Appendix C, and will make reasonable efforts to conduct the
infant phase of the Phase I clinical trial, and Phase II and Phase III clinical
trials.
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(13) Xxxxxxx X. Xxxxxx M.D. shall be responsible for
supervising the adult clinical trials at XXXXXX and shall be designated as
"Principal Adult Investigator." Xxxxx X. Xxxxxxxxx, M.D. shall be responsible
for supervising the pediatric clinical trials at XXXXXX and shall be designated
as "Principal Pediatric Investigator." In the event that either such
investigator is disabled or no longer employed at XXXXXX, then XXXXXX shall have
the right to appoint another such investigator, subject to approval by VRI which
shall not be unreasonably withheld.
(14) XXXXXX and VRI agree to conduct the clinical trials
according to the protocols. However, if at any future date, changes in the
protocol appear desirable, such changes may be made through prior written mutual
agreement between XXXXXX and VRI. The clinical trials may be suspended or
terminated, as appropriate, at any time by XXXXXX if in the reasonable medical
judgment of either: the Principal Adult or Pediatric Investigator, or
responsible institutional review board(s) or in the medical and/or regulatory
judgment of VRI the health or safety of patients will be adversely affected and
it is appropriate to do so. Any action taken by XXXXXX or its investigators or
employees based on any such medical judgment shall not be deemed a breach of
this AGREEMENT.
(15) XXXXXX agrees that the rights and welfare of the human
subjects shall be protected in accordance with the protocols and all applicable
federal and state laws. XXXXXX shall be responsible for obtaining appropriate
institutional review board approval for the protocols and any subsequent changes
to the protocols, and for obtaining informed consent of each human subject
participating in the protocols. XXXXXX shall retain records of the clinical
trials including the original of all volunteer consent forms in accordance with
all federal regulations.
(16) In order to maintain subject confidentiality, no
information relative to subject name or address shall be provided to VRI. All
patient information will be identified in code. Any audits conducted by VRI
shall be undertaken in conjunction with XXXXXX in order to ensure
confidentiality.
(17) VRI shall promptly advise XXXXXX of adverse reactions or
side effects relating to clinical trials which may become known to VRI and,
similarly XXXXXX shall promptly advise VRI of adverse reactions or side effects
relating to clinical trials which may become known to XXXXXX.
(c) If XXXXXX fails to perform any of its obligations under this
Section 3.1 and any such failure is not cured following sixty (60) days written
notice to XXXXXX, VRI may terminate XXXXXX'x services relating to the
obligations in the relevant Section (Sections 3.1 (b) (1-17)) of this Section
and VRI shall thereafter have the right to hire a third party contractor at
VRI's expense to perform and control the performance of such services.
Termination of services provided herein in Sections 3.1 (b) (1-17) shall not
affect the rights and obligations of XXXXXX under any other Section. Upon
termination of XXXXXX'x services for the foregoing reasons VRI will be obligated
to pay XXXXXX for all pre-approved costs of the studies incurred by XXXXXX and
not capable of cancellation. Such payment will be made within 30 days of
submission of billing by XXXXXX to VRI. At VRI's request, XXXXXX will assist VRI
in selecting and approving such third party contractors to perform functions
described in this Section 3.1.
(d) Notwithstanding the foregoing, VRI, as sponsor of the
development program may terminate XXXXXX services in conducting clinical trials
for commercial reasons at any time with 30 days' notice subject to VRI's payment
of all non-cancelable, pre-approved costs within 30 days of XXXXXX'x billing to
VRI.
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3.2 VRI agrees to pay XXXXXX for all fees and expenses that XXXXXX expects
to reasonably incur in conducting the trials described in Section 3.1 above,
provided that the amounts of such fees and costs have been approved by VRI in
writing in advance. VRI agrees to pay 40% of the approved budget for each study
in phase I, II and III upon initiation of each study and the remaining 60% at
agreed upon milestones during the course of each study, so that full payment for
each study is made by the conclusion of that study. Irrespective of the amount
advanced, VRI shall pay all costs incurred by XXXXXX in conducting the trials
described in Section 3.1, provided such expenses have been approved in advance
by VRI. If the monies advanced by VRI exceed expenses for a study, XXXXXX shall
refund the difference. VRI shall have the trials monitored by its own staff or
outside contractors at its election and shall have the data resulting from the
studies compiled and analyzed. VRI shall have any such VRI staff or outside
contractors execute a confidentiality agreement, prior to such staff or outside
contractors involvement in the clinical trials.
3.3 XXXXXX and/or its investigators will have the right to publish the
results of the clinical trials described in Section 3.1 above and performed by
XXXXXX, provided that VRI is provided with a preprint and/or abstract of any
proposed publication at least forty-five (45) days in advance of submission of
the proposed publication. In the event that, as a result of reviewing such
abstract or preprint, VRI determines that such publication would result in
disclosure of an Invention as to which VRI has rights under Sections 2.1, 2.4
and/or 2.5 hereof or includes any VRI Confidential Information (as hereinafter
defined), XXXXXX agrees to delay publication for a sufficient period to enable a
patent application to be filed with respect thereto at VRI's expense and delete
VRI confidential information, VRI acknowledges and agrees that XXXXXX and/or its
investigators will be entitled to appropriate credit, and to be included as
co-authors for those directly involved in the study, in accordance with
prevailing scientific standards.
3.4 In lieu of VRI paying minimum royalties and subject to obtaining FDA
or foreign regulatory approval for the 89-12 rotavirus vaccine VRI agrees to use
reasonable efforts to bring one or more Licensed Products to the marketplace
through a program of development; production, distribution, and marketing
consistent with sound and reasonable business practices and judgments. VRI
agrees to provide XXXXXX annually with a business development plan (which will
include strategy, major milestones for clinical development, FDA registration,
commercialization, and financial performance data) for the upcoming fiscal year,
the first plan due no later than one hundred eighty (180) days from the
Effective Date hereof and each subsequent plan due no later than December 31 in
subsequent years. In the event XXXXXX believes VRI is not exerting reasonable
efforts XXXXXX shall advise VRI and state the efforts which it believes would
meet this requirement. If VRI disagrees the parties will attempt to resolve the
matter by good faith discussions. If they still cannot agree the matter shall be
submitted to arbitration pursuant to Section 12 to determine the efforts to be
exerted by VRI. After the arbitration decision, in the event VRI fails to exert
the efforts required by the arbitration, XXXXXX shall have the right to
terminate this AGREEMENT upon giving VRI thirty (30) days prior written notice
and the opportunity to cure within said thirty (30) days or alternatively VRI
may resume minimum royalty payments in lieu of preparation of a business plan
and using reasonable efforts; however, in such event, resumption of payment of
minimum royalties under this Section 3.4 does not entitle VRI to an exclusive
license agreement.
4. PAYMENTS.
4.1 (a) VRI agrees to pay XXXXXX in partial consideration for the license
granted hereunder a licensing fee in the total amount of $50,000 payable in two
equal installments, as follows:
(1) upon signing of this AGREEMENT $25,000
(2) upon filing of the PLA/NDA for a Licensed $25,000
Product with the FDA
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4.2 (a) VRI shall pay the following running royalties to XXXXXX during the
term of this AGREEMENT as set forth below:
(1) Five percent (5%) on the Net Sales by VRI or its
Affiliates of Licensed Products or any use of Licensed Processes in the United
States (other than sales to Sublicensees for resale) where the manufacture, use
or sale of such Licensed Products or any use of such Licensed Processes is
covered by a Valid Claim of Patent Rights; or four percent (4%) on such Net
Sales in countries other than the United States (other than sales to
Sublicensees for resale) where the manufacture, use or sale of Licensed Products
or any use of Licensed Processes is covered by a Valid Claim of Patent Rights in
the country of sale; or one percent (1%) of Net Sales for five (5) years from
first commercial sale in a country, on a country by country basis, on any other
sales by VRI or its Affiliates of Licensed Products (other than sales to
Sublicensees for resale) where no Patent Rights have been nor are intended to be
filed with respect to such products; or two percent (2%) of Net Sales of
Licensed Products sold to the United States Government or sold to State or other
agencies at equivalent prices to those established for sale to the United States
Government.
(2) From any royalties received from its Sublicensees, VRI
shall pay XXXXXX thirty (30%) of royalties received by VRI from a Sublicensee
for sale of Licensed Products. Reporting and payment of such royalties shall be
made in accordance with the provisions of Section 5.
(3) If royalties for Licensed Products or Licensed Processes
covered by a Valid Claim of Patent Rights cease to be paid because a patent
application has been pending for more than five (5) years from the relevant U.S.
priority date, then a royalty of 1% of Net Sales will be payable until the end
of the fifth year on the market in that country. No royalty will be payable
following the fifth anniversary of first marketing in that country unless a
valid and enforceable patent subsequently issues. If a valid and enforceable
patent issues royalties will be payable from the date of issue until the expiry
of said valid and enforceable patent at the full applicable royalty rate for
that country as set forth in Section 4.2(1).
4.3 (a) Subject to Section 3.4, during the exclusive period of the
AGREEMENT, VRI shall pay a minimum annual royalty commencing on the expiration
of calendar year 1999 and continuing through calendar year 2003, as follows:
1999 $100,000
2000 $200,000
2001 $300,000
2002 $400,000
2003 $500,000
(b) If the royalties earned and paid to XXXXXX pursuant to Section
4.2 (a) for any of the above calendar years are not at least equal to the
applicable minimum royalties, VRI shall have the right to pay any difference
between such minimum royalty amounts and the royalties paid to XXXXXX in full
satisfaction of such obligation under this Section 4.3, which payment, if any,
shall be made with the quarterly royalty payment due for the last quarter of the
applicable calendar year. Waiver of any minimum royalty payment by XXXXXX shall
not be construed as a waiver of any such subsequent payment. If VRI fails to
make any such minimum royalty payment, XXXXXX shall have the right, at its
option, to convert the License for the Licensed Products and Licensed Processes
under Section 2.1 to a non-exclusive license. Royalty rates for non-exclusive
licenses shall be fifty percent (5 0%) of the exclusive rates set forth in
Section 4.2(a).
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4.4 (a) In the event that a Licensed Product under this AGREEMENT is sold
in any country in a combination package or kit containing other active products
not licensed hereunder, the Net Sales in each such country for purposes of
determining royalty payments on the combination package, shall be calculated
using one of the following methods:
(1) By multiplying the net selling price of that combination
package by the fraction A/A+B, where A is the net selling price in such
country during the royalty-paying period in question, of the Licensed Product
sold separately or Licensed Process used separately, and B is the net selling
price in such country during the royalty period in question, of the other active
products sold separately or used separately.
(2) In the event that no such separate sales are made of the
Licensed Product or any of the active products in such combination package in
such country during the royalty-paying period in question, Net Sales for the
purposes of determining royalty payments, shall be calculated by dividing the
net selling price in such country of the combination package by the number of
functions performed by the combination package sold where such package contains
active agents or other proprietary technology other than those licensed under
this AGREEMENT.
4.5 Payment of royalties specified in Section 4.2 (a) shall be made by VRI
to XXXXXX within sixty (60) days after March 31, June 30, September 30 and
December 31 each year during the term of this AGREEMENT covering the quantity of
Licensed Products sold or Licensed Processes used by VRI during the preceding
calendar quarter. The last such payment shall be made within sixty (60) days
after termination or expiration of this AGREEMENT.
4.6 All payments to be made under this Section shall be paid in United
States dollars at such a place and in such a way, as XXXXXX may reasonably
designate, without deduction of exchange, collection or other charges.
Conversion of foreign currency to U.S. dollars shall be made at the conversion
rate published by the Bank of Boston on the last day of the calendar quarter
with respect to which payments are due.
4.7 Only a single royalty shall be paid with respect to any Licensed
Product or Licensed Process, under Section 4.2(a) irrespective of the number of
Valid Claims of Patent Rights utilized.
4.8 In the event that VRI is required to pay royalties to one or more
third parties under patents other than Patent Rights in order to make, use, sell
or have sold Licensed Products or Licensed Processes, VRI shall be entitled to a
credit against royalties due XXXXXX under Section 4.2(a) in an amount equal to
fifty percent ( 50%) of the royalties paid to such third parties. However, in no
event shall royalties payable to XXXXXX under Section 4.2(a) hereunder be
reduced by more than forty percent (40%).
4.9 If the transfer of or the conversion into the United States dollar
equivalent of any remittance due hereunder is not lawful or permissible in any
county, such remittance shall be made thereof in the currency of the country to
the credit and account of XXXXXX or its nominee in any commercial bank located
in that country. Prompt notice shall be given to XXXXXX and XXXXXX may provide a
nominee if so desired.
4.10 If VRI exercises its option for the rights to improvements, VRI shall
reimburse XXXXXX for the cost of the development program to make such
Improvements.
5. REPORTS AND RECORDS
5.1 VRI shall maintain true books of account containing an accurate record
of all data necessary for the determination of the amounts payable under Section
4 hereof. Said records shall be kept at VRI's principal place of business or the
principal place of business of the appropriate division of VRI to
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which this AGREEMENT relates. Said records shall be available for inspection by
a certified public accountant selected and paid by XXXXXX once each year during
regular business hours and for six (6) years thereafter following the end of the
calendar year to which they pertain in order for XXXXXX to ascertain the
correctness of any report and/or payment made under this AGREEMENT. The
provision of this Section 5.1 shall survive termination of this AGREEMENT.
5.2 (a) Commencing with the calendar quarter in which Net Sales first
occurs, sixty (60) days after March 31, June 30, September 30 and December 31,
of each year in which this AGREEMENT is in effect, VRI shall deliver to XXXXXX
full, true and accurate reports of its activities and those of its
Sublicensee(s), if any, relating to this AGREEMENT during the preceding three
month period. These reports shall include at least the following:
(1) Gross Sales for Licensed Products or Licensed
Processes;
(2) Net Sales for Licensed Products or Licensed
Processes
(3) Expenses, defined in Section 1.7, used to
calculate Net Sales;
(4) Calculation of royalties due based on Net Sales;
(5) Any adjustments to amounts due pursuant to this
AGREEMENT; and
(6) Amounts due to XXXXXX for the applicable quarters.
5.3 With each such report, VRI shall pay to XXXXXX the royalties due and
payable as provided for in Section 4.5. If no royalties are due under Section
4.2(a), VRI shall so report.
6. PATENT PROSECUTION AND INFRINGEMENT.
6.1 XXXXXX shall apply for and maintain during the term of this AGREEMENT
any Patent Rights in the United States and in the European Union, Australia,
Brazil, Canada, Japan and South Korea, and Mexico. The prosecution, filing and
maintenance of all patents, with the exception of fee payments, shall be the
primary responsibility of XXXXXX, using patent counsel selected by XXXXXX and
reasonably acceptable to VRI, provided, however, that VRI shall be given a
reasonable opportunity to advise XXXXXX on such matters, particularly as they
pertain to patent prosecution in foreign countries, and XXXXXX shall furnish to
VRI copies of any documents relevant to such prosecution, filing and maintenance
in sufficient time in advance for VRI or its patent counsel to comment thereon.
VRI shall pay all reasonable patent fees and costs, including reasonable counsel
fees, incurred by XXXXXX pursuant to this Section.
6.2 VRI has reimbursed XXXXXX the sum of $24,277, representing 50% of
foreign phase filing costs for the countries and listed in Section 6.1. VRI
shall reimburse XXXXXX the sum of $78,558 upon VRI signing this AGREEMENT for
the remaining 50% of the foreign phase filing costs and for its U.S. patent fees
and costs arising from the Patent Rights invoiced by patent counsel to XXXXXX
prior to October 10, 1994. All fees and costs incurred by XXXXXX after the
Effective Date relating to the filing, prosecution and maintenance of all Patent
Rights shall be paid by VRI within 30 days of receipt of invoice from XXXXXX.
The foregoing notwithstanding, VRI shall will have the right to discontinue
payment of any such fees or costs with respect to the Patent Rights in any
particular country or countries, if after a good faith assessment of the cost of
patent filing, the enforceability of intellectual property rights and the
10
commercial value of the market, in a specific country, VRI believes that making
such payments would not be commercially practical. VRI shall provide timely
notice of VRI's intention not to pay a fees so, if XXXXXX desires, XXXXXX may
pay such fee.
6.3 If at any time during the term of this AGREEMENT, VRI furnishes to
XXXXXX reasonably convincing written evidence of an infringement of a patent
included in the Patent Rights which adversely and substantially affects the
commercial operations of VRI under the license granted hereunder, XXXXXX shall
have the right, but not the obligation, to prosecute, at its own expense any
such infringement and shall have the right for such purpose to join VRI as a
party plaintiff at XXXXXX'x expense. VRI independently shall have the right to
join any such suit or action brought by XXXXXX and, in such event, shall pay
one-half of the cost of such suit or action from the date of joining. Provided
that VRI has joined in the action and shared the costs thereof as stated in the
preceding sentence, no settlement, consent judgment or other voluntary final
disposition of the suit may be entered into without the consent of VRI, which
consent will not unreasonably be withheld. Any recovery or damages derived from
such action shall first be used to reimburse XXXXXX for all legal expenses
relating to such action. If VRI has not joined the action, XXXXXX is entitled to
all recovery or damages still remaining; however, if VRI has joined the action,
any recovery or damages still remaining shall be applied toward (i)
reimbursement of XXXXXX for the amount of royalties not received by XXXXXX from
the infringing party as a result of such infringement, and (ii) compensation of
VRI for its lost profits or a reasonable royalty on the sales of the infringer,
whichever is applicable; provided, however that if such remaining amount of
recovery or damages is insufficient to compensate XXXXXX fully for such
royalties and to compensate VRI fully for such lost profits or reasonable
royalty, then such amount of recovery or damages still remaining shall be
apportioned pro rata between XXXXXX and VRI in proportion to (a) the amount of
royalties not received by XXXXXX from the infringing party as a result of such
infringement, as compared with (b) VRI's lost profits or reasonable royalty on
the sales of the infringer. Any recovery or damages still remaining after the
above-mentioned applications shall be distributed two-thirds (2/3) to XXXXXX and
one-third (1/3) to VRI.
6.4 If after said three (3) months, XXXXXX fails to cause such
infringement to terminate or to bring a suit or action to compel termination,
VRI shall have the right, but not the obligation, to prosecute, at its own
expense any such infringement and shall have the right for such purpose to join
XXXXXX as a party plaintiff at VRI's expense. XXXXXX independently shall have
the right to join any such suit or action brought by VRI and, in such event,
shall pay one-half of the cost of such suit or action from the date of joining.
Provided that XXXXXX has joined in the action and shared the costs thereof as
stated in the preceding sentence, no settlement, consent judgment or other
voluntary final disposition of the suit may be entered into without the consent
of XXXXXX, which consent will not unreasonably be withheld. Any recovery or
damages derived from such action shall first be used to reimburse VRI (and
XXXXXX if it joined in the action) for all legal expenses relating to such
action. If XXXXXX has not joined the action, VRI is entitled to all recovery or
damages still remaining; however, if XXXXXX has joined the action, any recovery
or damages still remaining shall be applied toward (i) reimbursement of XXXXXX
for the amount of royalties not received by XXXXXX from the infringing party as
a result of such infringement, and (ii) compensation of VRI for its lost profits
or a reasonable royalty on the sales of the infringer, whichever is applicable;
provided, however that if such remaining amount of recovery or damages is
insufficient to compensate XXXXXX fully for such royalties and to compensate VRI
fully for such lost profits or reasonable royalty, then such amount of recovery
or damages still remaining shall be apportioned pro rata between XXXXXX and VRI
in proportion to (a) the amount of royalties not received by XXXXXX from the
infringing party as a result of such infringement, as compared with (b) VRI's
lost profits or reasonable royalty on the sales of the infringer. Any recovery
or damages still remaining after the above-mentioned applications shall be
distributed two-thirds (2/3) to XXXXXX and one-third (1/3) to VRI.
6.5 In any infringement suit that either party may institute to enforce
the Patent Rights pursuant to this AGREEMENT, the other party hereto shall,
cooperate in all respects and, to the extent
11
possible, have its employees testify when requested and make available relevant
records, papers, information, samples and the like.
6.6 In the event that a declaratory judgment action alleging invalidity or
non-infringement of any of the Patent Rights shall be brought against VRI,
XXXXXX, at its sole option shall have the right, within sixty (60) days after
XXXXXX receives notice from VRI of such action, to intervene and participate in
action at its own expense.
7. TERM AND TERMINATION.
7.1 Unless earlier terminated as provided herein, this AGREEMENT shall
remain in full force and effect for the life of the last to expire patent issued
under the Patent Rights. Upon expiration, VRI shall have a fully paid-up,
non-cancelable license.
7.2 Subject to Section 16, if VRI shall cease to carry on its business,
this AGREEMENT shall terminate ninety (90) days after VRI ceases to do business,
unless, within ninety (90) days VRI has identified a qualified successor
licensee reasonably acceptable to XXXXXX willing to assume the obligation of VRI
hereunder, in which case the assignment of this AGREEMENT to such successor
licensee shall be subject to the written assumption by such successor of VRI's
obligations hereunder and to the written approval of XXXXXX, which shall not be
unreasonably withheld.
7.3 Should VRI fail to pay XXXXXX such royalties other than minimum
royalties as are due and payable hereunder, XXXXXX shall have the right to
terminate this AGREEMENT on thirty (30) days written notice, or to convert this
AGREEMENT from an exclusive to a non-exclusive license upon expiration of the
thirty (30) day period.
7.4 VRI shall have the right to terminate this AGREEMENT at any time upon
six (6) months written notice to XXXXXX, and upon payment of all amounts due
XXXXXX through the effective date of termination. If this AGREEMENT is
terminated, VRI will provide XXXXXX with information and data necessary for
XXXXXX to pursue the development of Licensed Products or Licensed Processes and
a right to reference VRI's regulatory filings with the FDA.
7.5 Upon any material breach or default of this AGREEMENT by VRI or
XXXXXX, the non-breaching party shall have the right to terminate this AGREEMENT
and the rights, privileges and license hereunder granted upon ninety (90) days
written notice to the other party. Such termination shall become effective
immediately at the conclusion of such notice period unless the breaching party
shall have cured any such breach or default prior to the expiration of the
ninety (90) day period.
7.6 Upon termination of this AGREEMENT for any reason, nothing herein
shall be construed to release either party from any obligation that matured
prior to the effective date of such termination. VRI and any Sublicensee thereof
may, after the effective date of such termination, sell all Licensed Products
which are in inventory at the time of termination, and complete and sell
Licensed Products which VRI can clearly demonstrate were in the process of
manufacture at the time of such termination, provided that VRI shall pay to
XXXXXX the royalties thereon as required by Section 4 of this AGREEMENT and
shall submit the reports required by Section 5 hereof on the sales of Licensed
Products.
12
8. INDEMNIFICATION AND INSURANCE.
8.1 VRI shall defend, indemnify and hold harmless XXXXXX and its trustees,
officers, medical and professional staff, employees, and agents and their
respective successors, heirs and assigns, against all losses, damages, expenses,
including attorney's fees and against any claims, suits, actions, demands or
judgments brought against any one or more of them, arising out of any theory of
product liability (including, but not limited to, actions in the form of tort,
warranty, or strict liability) or negligence concerning any product, process or
service made, used or sold pursuant to any right or license granted under this
AGREEMENT. VRI shall have the right to control the defense settlement and/or
compromise of any such claims or actions.
8.2 VRI's obligations under Section 8.1 above shall not apply to any
liability, damage, loss or expense to the extent that it is directly
attributable to the negligence or intentional misconduct of XXXXXX or of any of
its trustees, officers, medical and professional staff, employees, agents or
their respective successors, heirs or assigns.
8.3 VRI shall add, at VRI's expense, XXXXXX as an additional insured on
VRI's clinical trial insurance policy, which provides limits of liability of
$2,000,000 per incident and aggregate, effective upon the Effective Date of this
AGREEMENT, to provide insurance coverage for XXXXXX for the clinical trials.
8.4 VRI, at VRI's expense, shall maintain policies of comprehensive
general liability insurance and will obtain product liability insurance in
amounts not less than $1,000,000 per incident and $2,000,000 annual aggregate
and shall add XXXXXX as an additional insured on VRI's policy, which provides
such limits of liability. Such insurance shall provide (i) product liability
coverage, (ii) negligence, and (iii) broad form contractual liability coverage,
for VRI's indemnification under Section 8.1 of this AGREEMENT. The minimum
amounts of insurance coverage required under these provisions shall not be
construed to create a limit of VRI's liability with respect to VRI's
indemnification obligation under Section 8.1 of this AGREEMENT. VRI shall
maintain such comprehensive general liability insurance and product liability
insurance beyond the expiration or termination of this AGREEMENT and for a
reasonable period after the termination of the clinical trials, which in no
event shall be less than fifteen (15) years after the clinical trials.
8.5 This Section 8 shall survive expiration or termination of this
AGREEMENT.
9. REPRESENTATIONS
9.1 Subject to any prior rights of the U.S. government, XXXXXX represents
that patent applications or patents included in the Patent Rights have been
assigned to it and that XXXXXX has the authority and power to issue licenses
under said Patent Rights and that XXXXXX has the right to disclose Technical
Information to VRI and to enter into and perform this AGREEMENT.
9.2 XXXXXX does not warrant the validity of the Patent Rights licensed
hereunder and makes no representation whatsoever with regard to the scope of the
Patent Rights or that such Patent Rights may be exploited by VRI, its
Affiliates, or Sublicensees without infringing other patents, except that XXXXXX
represents that as of the Effective Date it is not aware of any patent or patent
application not a part of the Patent Rights licensed hereunder that would be
infringed by the exercise by VRI, its Affiliates or Sublicensees, of the rights
granted to them hereunder.
13
10. CONFIDENTIALITY.
10.1 Confidential Information. As used in this AGREEMENT, "Confidential
Information" means all information transmitted by a party hereto or obtained by
a party hereto in connection with the performance of the clinical trials and
other services described in Section 3 hereof or of any such other services to be
provided by the parties as described herein, subject to the exceptions specified
below. "Confidential Information" means information of any type, not generally
known, about the business processes, services, products, suppliers, customers,
clients or plans of XXXXXX or VRI ("the parties hereto") of any client of The
parties hereto (regardless of whether the parties hereto have executed a
confidentiality agreement with such customer), which is used or useful in the
conduct of business of the parties hereto, or which confers or tends to confer a
competitive advantage over one who does not possess such information. Such
information includes, but is not limited to, information relating to trade
secrets, Technical Information, patent applications, know-how, research,
development, design, engineering, quality control or service techniques,
information about existing, new or envisioned products, processes or services
and their development, performance, scientific, engineering or technical
information, laboratory notebooks, notes, computer programs, source codes,
object codes, software manuals, sketches, drawings, reports, formulae, gels,
slides, sequences, biological materials living or otherwise, photographs,
negatives, prototypes, models, correspondence, and other documents and things,
and information relating to purchasing, sales, marketing, licensing, contracts
with third parties, and pricing, whether or not in writing and whether or not
labeled or identified as confidential or proprietary. Confidential Information
may be disclosed in writing or orally or may be obtained by observation or
inspection. All data, materials, information, and records developed by a party
hereto in the course of performing this AGREEMENT shall be considered
Confidential Information. However, Confidential Information shall not include
information that a party hereto can demonstrate: (i) is in or enters the public
domain through no fault of such party; (ii) is disclosed to a party hereto by a
third party entitled to disclose it; (iii) was known to a party hereto before
the date of this AGREEMENT; or (iv) is required by law to be disclosed, provided
reasonable advance notice of such requirement is given to a party hereto before
such disclosure.
10.2 Confidentiality. Without prior written consent the parties hereto
will not disclose the other party's Confidential Information to any third party
other than employees, agents or others of the parties hereto who must
necessarily be informed thereof, but only if and to the extent that any such
person has a need for such information. A party hereto will only use
Confidential Information for the purpose of fulfilling its obligations under
this AGREEMENT. The parties hereto agree that they will take such reasonable
steps as may be necessary to prevent the disclosure or use of any such materials
by their officers, employees or agents except as provided herein, including but
not limited to obtaining and enforcing appropriate confidentiality agreements
with such persons. All obligations of confidentiality and nondisclosure set
forth in this AGREEMENT shall survive the termination or expiration of this
AGREEMENT.
10.3 The parties agree that clinical trial data generated by XXXXXX under
the terms of the AGREEMENT will not be published by VRI prior to its publication
by XXXXXX'x principal investigators. To the extent not published, the results of
the clinical trials will be held in confidence by XXXXXX. Subject to the
foregoing, VRI will have the unrestricted right to use or disclose such clinical
trial data.
14
11. NOTICES.
11.1 Reports, notices and other communications from VRI to XXXXXX as
provided hereunder shall be sent by certified mail to:
Xxxxx X. Xxxxxx Institute of Medical Research
0000 Xxxxxx Xxxxxx
Xxxxxxxxxx, XX 00000
Attention: President
or other individuals or addresses as shall hereafter be furnished by
written notice to VRI.
11.2 Reports, notices and other communications from XXXXXX to VRI as
provided hereunder shall be sent to by certified mail to:
Virus Research Institute, Inc.
00 Xxxxxxx Xxxxxx
Xxxxxxxxx, XX 00000
Attention: President
or other individuals or addresses as shall hereafter be furnished by
written notice to XXXXXX.
12. ARBITRATION.
12.1 (a) Any controversy, dispute or claim arising out of, or relating to,
any provisions, the interpretation or the performance of this AGREEMENT or any
breach thereof which cannot otherwise be resolved by good faith negotiations
between the parties shall be resolved by final and binding arbitration under the
rules of the American Arbitration Association, or the Patent Arbitration Rules,
if applicable, which are in effect as of the Effective Date of this AGREEMENT.
In the event that VRI initiates, requests and/or files for arbitration, the
arbitration shall be conducted in Cincinnati, Ohio. In the event that XXXXXX
initiates, requests and/or files for arbitration, the arbitration shall be
conducted in Boston, Massachusetts.
(b) The arbitration shall be subject to the following terms:
(1) The number of arbitrators shall be three (3).
(2) The arbitrators shall be independent; impartial third
parties having no direct or indirect personal or financial relationship to any
of the parties to the dispute, who has have agreed to accept the appointment as
arbitrator on the terms set out in this Section 12.1.
(3) The arbitrators shall be active or retired attorneys, law
professors, or judicial officers with at least five (5) years experience in
general commercial matters and a familiarity with the laws governing proprietary
rights in intellectual property and in particular patent law.
(4) The arbitrators shall be selected as follows:
(i) Each party shall submit a description of the inner
to be arbitrated to the American Arbitration Association at the appropriate
Regional Office in Cincinnati, Ohio or Boston, Massachusetts, depending upon
where the arbitration is to be held. Said Association shall submit to the
parties a list of the arbitrators available to arbitrate any dispute between
them. Thereafter,
15
each party shall select; in numerical order, those persons on said list
acceptable as arbitrators and return the same to the Association. The first
three arbitrators acceptable to both parties shall be deemed the selected
arbitrators with respect to the dispute then at issue under this AGREEMENT. In
the event of a failure to select three mutually agreeable arbitrators, the
Association shall be requested to submit as man subsequent lists of arbitrators
as shall be necessary to effect a mutual selection.
(ii) If the method of selection set out in Section 12.1
(b)(4)(a) fails for any reason, then either party may petition any state or
federal court in Massachusetts or Ohio having jurisdiction for appointment of
the arbitrators in accordance with applicable law, provided that the arbitrators
must satisfy the requirements of Sections 12.1 (b)(2) and 12.1 (b)(3) above and
be acceptable to each party hereto.
(5) The arbitrators shall announce the award in writing
accompanied by written findings explaining the facts determined in support of
the award, and any relevant conclusions of law.
(6) Unless otherwise provided in this Section 12.1 or extended
by agreement of the parties, each party shall submit an initial request for
designation of arbitrators within thirty (30) days after any request for
arbitration, the dispute shall be submitted to the arbitrators within sixty (60)
days after the arbitrators are selected, and a decision shall be rendered within
thirty (30) days after the dispute is submitted.
(7) The fees of the arbitrators and any other costs and fees
associated with the arbitration shall be paid in accordance with the decision of
the arbitrators.
(8) The arbitrators shall have no power to add to, subtract
from, or modify any of the terms or conditions of this AGREEMENT. Any award
rendered in such arbitration may be enforced by either party in either the
courts of the Commonwealth of Massachusetts or Ohio or in a United States
District Court for the District of Massachusetts or Ohio, to whose jurisdiction
for such purposes XXXXXX and VRI each hereby irrevocably consents and submits.
12.2 Notwithstanding the foregoing, nothing in this Section shall be
construed to waive any rights or timely performance of any obligations existing
under this AGREEMENT.
13. RESTRICTIONS ON USE OF NAMES.
VRI shall not use the names of XXXXXX, its related entities and its
employees, or any adaptations thereof, in any advertising, promotional or sales
literature, without the prior written consent of XXXXXX; provided however, that
VRI (a) may refer to publications by employees of XXXXXX in the scientific
literature or (b) may state that a license from XXXXXX has been granted as
herein provided.
14. INDEPENDENT CONTRACTOR.
For the purpose of this AGREEMENT and all services to be provided
hereunder, both parties shall be, and shall be deemed to be, independent
contractors and not agents or employees of the other. Neither party shall have
authority to make any statements, representations or commitments or any kind, or
to take any action, that will be binding on the other party.
16
15. SEVERABILITY.
If any one or more of the provisions of this AGREEMENT shall be held to be
invalid, illegal or unenforceable, the validity, legality or enforceability of
the remaining provisions of this AGREEMENT shall not in any way be affected or
impaired thereby.
16. NON-ASSIGNABILITY.
Neither this AGREEMENT nor any part hereof shall be assignable by either
party without the express written consent of the other provided that either VRI
or XXXXXX may assign this AGREEMENT in connection with the merger, consolidation
or sale of substantially all of its assets or the sale of that portion of its
business to which the Inventions relate or as set forth in Section 7.2 and
further provided that neither party shall unreasonably withhold its consent to
any other assignment by the other party to an assignee which can reasonably
demonstrate its qualifications to carry out the obligations of VRI or XXXXXX
hereunder. Any other attempted assignment without such consent shall be void.
17. ENTIRE AGREEMENT.
This instrument contains the entire AGREEMENT between the parties hereto.
No verbal agreement, conversation or representation between any officers,
agents, or employees of the parties hereto either before or after the execution
of this AGREEMENT shall affect or modify any of the terms or obligations herein
contained.
18. MODIFICATIONS IN WRITING.
No change, modification, extension, termination or waiver of this
AGREEMENT, or any of the provisions herein contained, shall be valid unless made
in writing and signed by a duly authorized representative of each party.
19. GOVERNING LAW.
The validity and interpretation of this AGREEMENT and the legal relations
of the parties to it shall be governed by the laws of the State of Ohio.
20. CAPTIONS.
The captions are provided for convenience and are not to be used in
construing this AGREEMENT.
21. PATENT MARKING
VRI agrees to xxxx and have marked all Licensed Products sold by it under
the license granted herein, if practical, with the word "Patent" or "Patents"
and the number of the patent or patents applicable thereto.
17
IN WITNESS WHEREOF, the parties hereto have caused this AGREEMENT to be
executed in quadruplicate by their duly authorized representatives as of the
date first above written.
XXXXX X. XXXXXX INSTITUTE VIRUS RESEARCH INSTITUTE, INC.
(XXXXXX) (VRI)
By: /s/ Xxxxxxx X. Xxxxxx By: /s/ Xxxxxxx X. Xxxxxx
--------------------------------- ---------------------------------
Xxxxxxx X. Xxxxxx M.D. Xxxxxxx X. Xxxxxx
Title: President Title: President
WITNESSED BY: W1TNESSED BY:
/s/ [ILLEGIBLE] /s/ [ILLEGIBLE]
------------------------------------- -------------------------------------
18
APPENDIX A
LIST OF PATENT APPLICATIONS INCLUDED IN THE PATENT RIGHTS
1.) U.S. Serial No. 07/614,310, filed November 16, 1990, entitled "Human
Rotaviruses, Vaccines and Methods," and invented by Xxxxxxx X. Xxxx.
2.) U.S. Serial No. 07/816,974, filed January 3, 1992, entitled "Human
Rotaviruses, Vaccines and Methods," and invented by Xxxxxxx X. Xxxx
(Division of U.S. Serial No. 07/614,310).
3.) Serial No. PCT/U.S. 91/08191, filed November 4, 1990, entitled "Human
Rotaviruses, Vaccines and Methods," and invented by Xxxxxxx X. Xxxx.
U.S. Patent Application Serial Number 08/143975
U.S. Patent Application Serial Number 08/114114
Brazilian Patent Application Serial Number 9106982
European Patent Application Serial Number 92900590.8
Mexican Patent Application Serial Number 9303196
Australian Application Serial Number 90603/91
Canadian Application Serial Number 2096315
S. Korean Application Serial Number 00000000
Japanese Application Serial Number 501860/92
19
APPENDIX B
MATERIALS TRANSFER AGREEMENT
THIS AGREEMENT entered the day of 19 , by and between the Xxxxx
X. Xxxxxx Institute of Medical Research ("Provider"), a non-profit corporation
having a place of business at 0000 Xxxxxx Xxx., Xxxxxxxxxx, Xxxx 00000 and ***
("Recipient"), a corporation having a place of business at .
1. Subject to availability Provider agrees to provide the following material
to recipient: ***. Such material and any related biological material or
associated know-how and data that will be received by Recipient from
Provider, and any substance that is replicated or derived therefrom are
covered by this Agreement. All such materials shall hereinafter be
referred to as the "Material(s)."
2. The Materials will be used by Recipient in connection with the research
described in Appendix A and only for non-commercial purposes. The
Materials shall not be used in research that is subject to consulting or
licensing obligations to another institution, corporation or business
entity, unless written permission is obtained in advance from Provider.
3. Recipient shall not distribute, release or disclose the Materials to any
other person or entity and shall ensure that no one will be allowed to
take or send the Materials to any other location, unless written
permission is obtained in advance from Provider. Recipient agrees to
maintain the confidentiality of any propriety information of Provider
regarding the Materials.
4. The Materials are supplied solely for scientific research purposes, for
use in animals and/or in vitro. THE MATERIALS SHALL NOT BE USED IN HUMANS.
5. No right or license is granted under the Agreement either expressly or by
implication. It is understood that any and all proprietary rights,
including but not limited to patent rights, in and to the Materials shall
be and remain in Provider.
6. Recipient agrees to provide Provider with an advance copy at least thirty
(30) days in advance of any written submission (abstract or paper) or oral
presentation that makes reference to the Materials. If in the opinion of
Provider any such publication describes a patentable development, Provider
shall have an opportunity to request that Recipient delay the submission
or public presentation until after a U.S. patent application has been
filed. In no event shall the delay be unreasonable. If a publication does
result from work using the Materials, Recipient agrees to acknowledge
Provider and/or give credit to Provider's scientists, as scientifically
appropriate, based on any direct contribution they may have made to the
work.
20
7. Recipient agrees not to sequence or clone any Material provided by
Provider without the written permission of Provider.
8. In the event that use of the Material results in an invention,
improvement, substance, or information whether or not patentable and
patents, if any, which result therefrom ("Developed Technology"),
Recipient agrees to disclose promptly to Provider all such inventions,
improvements or substances.
9. Recipient shall assign all right, title and interest in and to Developed
Technology to Provider. Recipient agrees to cooperate and assist Provider
in obtaining patent protection for Developed Technology.
10. Recipient agrees to execute, acknowledge and deliver all such further
papers as may be necessary to perform its obligation under this Agreement
11. Recipient acknowledges that the Materials are provided WITHOUT WARRANTY OF
MERCHANTABILITY OR FITNESS FOR A PARTICULAR PURPOSE OR ANY OTHER WARRANTY,
EXPRESS OR IMPLIED. PROVIDER MAKES NO REPRESENTATION THAT THE USE OF THE
MATERIALS WILL NOT INFRINGE ANY PATENT, COPYRIGHT, TRADEMARK OR OTHER
PROPRIETARY RIGHT.
12. In no event shall Provider be liable for any use of the Materials by
Recipient. Recipient hereby agrees to defend, indemnify and hold harmless
Provider, its officers, directors, trustees, employees and agents from any
loss, claim, damage, expense or liability, of whatsoever kind or nature
(including attorney's fees), which may arise from or in connection with
this Agreement or the use, handling or storage of the Materials.
13. Recipient shall report to Provider a summary of the results of Recipient's
work utilizing the Materials.
14. Upon the request of Provider, Recipient shall promptly return to Provider
the Materials furnished to Recipient under this Agreement.
15. Recipient agrees to comply with all government and National Institutes of
Health regulations and guidelines which are applicable to the Recipient's
use of the Materials.
16. This Agreement is not assignable, whether by operation of law or
otherwise, without the prior written consent of Provider.
21
IN WITNESS WHEREOF, the parties, intending to be legally bound, have caused this
Agreement to be executed by their respective duly authorized representatives.
RECIPIENT'S AUTHORIZED REPRESENTATIVE
INVESTIGATOR FOR RECIPIENT
BY: ____________________________ BY: ____________________________
________________________________ ________________________________
Typed Name Typed Name
________________________________ ________________________________
Title Title
PROVIDER'S AUTHORIZED REPRESENTATIVE
INVESTIGATOR FOR PROVIDER
BY: ____________________________ BY: ____________________________
________________________________ ________________________________
Typed Name Typed Name
________________________________ ________________________________
Title Title
22
APPENDIX C
PROTOCOL
REACTIVITY AND IMMUNOGENICITY OF LIVE, ATTENUATED
ROTAVIRUS VACCINE CANDIDATE 89-12
A copy of the protocol will be attached to the execution copy of this AGREEMENT
23
