EXCLUSIVE LICENSE AGREEMENT by and between AMGEN INC. and PINTA BIOSCIENCES, INC. Dated as of September 7, 2012

EXCLUSIVE LICENSE AGREEMENT by and between AMGEN INC. and PINTA BIOSCIENCES, INC. Dated as of September 7, 2012

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[*] = Certain confidential information contained in this document, marked by brackets, has been omitted and filed separately with the Securities and Exchange Commission pursuant to Rule 406 of the Securities Act of 1933, as amended.

Exhibit 10.19

EXCLUSIVE LICENSE AGREEMENT

by and between

AMGEN INC.

and

PINTA BIOSCIENCES, INC.

Dated as of September 7, 2012


ARTICLE 1	DEFINITIONS	1
ARTICLE 2	LICENSE GRANT; CLOSING	9
Section 2.1	Grant	9
Section 2.2	Sublicenses	10
Section 2.3	Right of Notification	10
Section 2.4	Transfer of Licensed Know-How and Licensed Materials	11
Section 2.5	Intentionally omitted	12
Section 2.6	No Other Rights	12
Section 2.7	Limited Exploitation Rights	13
ARTICLE 3	FEES, ROYALTIES AND PAYMENTS	13
Section 3.1	Upfront Payment	13
Section 3.2	Inventory Payment	13
Section 3.3	Milestone Payments	13
Section 3.4	Royalties	13
Section 3.5	Product Sublicensing Income	14
Section 3.6	Method of Payment; Royalty Reporting	14
Section 3.7	Currency Conversion	14
Section 3.8	Late Payments	15
Section 3.9	Records and Audits	15
Section 3.10	Taxes	16
ARTICLE 4	PATENT PROSECUTION, MAINTENANCE AND INFRINGEMENT	16
Section 4.1	Prosecution and Maintenance	16
Section 4.2	Amgen Step-1n Right	16
Section 4.3	Enforcement	17
Section 4.4	Defense of Third Party Claims	18
Section 4.5	Recovery	19
Section 4.6	Patent Term Extensions and Filings for Regulatory Exclusivity Periods	19
Section 4.7	Patent Marking	19
ARTICLE 5	OBLIGATIONS OF THE PARTIES	20
Section 5.1	Responsibility	20
Section 5.2	Diligence	20
Section 5.3	Reports	20
Section 5.4	Product Supply	20
Section 5.5	Pre-Existing Agreements	21
Section 5.6	Company Location	21
ARTICLE 6	EX-TERRITORY ACTIVITIES	22
Section 6.1	Rights to the Product in Jam	22
Section 6.2	Obligations under Japan Agreement	22
Section 6.3	License Grant and Right of Reference	22
Section 6.4	Product Data; Regulatory	22
Section 6.5	Amendment of Japan Agreement	23
ARTICLE 7	REPRESENTATIONS AND COVENANTS	23
Section 7.1	Mutual Warranties	23
Section 7.2	Additional Amgen Warranties	23


Section 7.3	Disclaimer	24
Section 7.4	Company Covenants	25
ARTICLE 8	INDEMNIFICATION	25
Section 8.1	Indemnity	25
Section 8.2	LIMITATION OF DAMAGES	26
Section 8.3	Insurance	27
ARTICLE 9	CONFIDENTIALITY	27
Section 9.1	Confidential Information	27
Section 9.2	Terms of this Agreement; Publicity	29
Section 9.3	Relationship to the Confidentiality Agreement	29
Section 9.4	Publications	30
ARTICLE 10	TERM AND TERMINATION	30
Section 10.1	Term	30
Section 10.2	Termination by Amgen	30
Section 10.3	Termination by Company	31
Section 10.4	Termination Upon Bankruptcy	32
Section 10.5	Effects of Termination	32
Section 10.6	Survival	33
ARTICLE 11	MISCELLANEOUS	34
Section 11.1	Entire Agreement; Amendment	34
Section 11.2	Section 365(n) of the Bankruptcy Code	34
Section 11.3	Independent Contractors	34
Section 11.4	Governing Law; Jurisdiction	34
Section 11.5	Notice	35
Section 11.6	Compliance With Law; Severability	35
Section 11.7	Non-Use of Names	35
Section 11.8	Successors and Assigns	36
Section 11.9	Sale Transaction or Amgen Acquisition	36
Section 11.10	Waivers	36
Section 11.11	No Third Party Beneficiaries	36
Section 11.12	Headings; Schedules	36
Section 11.13	Interpretation	37
Section 11.14	Counterparts	37

LIST OF SCHEDULES

Business Plan Schedule

Licensed Know-How Schedule

Licensed Materials Schedule

Licensed Patents Schedule

Milestones and Royalties Schedule

Permitted CMO Schedule

Pre-Existing Agreements Schedule

Press Release Schedule

Product Schedule

Quality Agreement Schedule

Specifications Schedule

Supply Agreement Schedule

EXCLUSIVE LICENSE AGREEMENT

This EXCLUSIVE LICENSE AGREEMENT (this “Agreement”) is entered into as of September 7, 2012 (the “Signing Date”) by and between AMGEN INC., a Delaware corporation having an address at Xxx Xxxxx Xxxxxx Xxxxx, Xxxxxxxx Xxxx, Xxxxxxxxxx 00000 (“Amgen”), and PINTA BIOSCIENCES, INC., a Delaware corporation (“Company”). Company and Amgen are sometimes referred to herein individually as a “Party” and collectively as the “Parties”.

RECITALS

WHEREAS, Amgen is a company engaged in the research, development, manufacturing and commercialization of pharmaceutical and biotechnology products;

WHEREAS, Amgen possesses certain rights to patents and other intellectual property related to its proprietary compound AMG 745, comprising the amino acid sequence set forth on the Product Schedule (the “Product”);

WHEREAS, Company desires to license from Amgen such intellectual property rights, and to commercially develop, manufacture, use and distribute the Product based upon the same throughout the Territory (defined below); and

WHEREAS, Amgen desires to grant such a license to Company in accordance with the terms and conditions of this Agreement.

NOW, THEREFORE, in consideration of the premises and the mutual promises and covenants contained in this Agreement, and for other good and valuable consideration, the receipt and sufficiency of which are hereby acknowledged, the Parties hereto agree as follows:

ARTICLE 1 DEFINITIONS

All references to particular Schedules, Articles or Sections shall mean the Schedules to, and Articles and Sections of, this Agreement, unless otherwise specified. For the purposes of this Agreement and the Schedules hereto, the following words and phrases shall have the following meanings:

“Abandoned Patent Right” has the meaning set forth in Section 4.2 (Amgen Step-In Right).

“Affiliate” means, with respect to any Person, any other Person which controls, is controlled by or is under common control with such Person, for as long as such control exists. For purposes of this Section, “control” means the direct or indirect ownership of more than fifty percent (50%) of the voting or economic interest of a Person, or the power, whether pursuant to contract, ownership of securities or otherwise, to direct the management and policies of a Person. For clarity, once a Person ceases to be an Affiliate of a Party, then, without any further action, such Person shall cease to have any rights, including license and sublicense rights, under this Agreement by reason of being an Affiliate of such Party.

“Agreement” has the meaning set forth in the Preamble.

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“Amgen” has the meaning set forth in the Preamble.

“Amgen Acquiree” has the meaning set forth in Section 11.9 (Sale Transaction or Amgen Acquisition).

“Amgen Acquisition” has the meaning set forth in Section 11.9 (Sale Transaction or Amgen Acquisition),

“Amgen Cell Line” shall mean the proprietary cell line that Amgen has developed for the generation of the Product. For avoidance of doubt, the Amgen Cell Line is a Licensed Material hereunder.

“Amgen Indemnified Parties” has the meaning set forth in Section 8.1.2 (By Company).

“Audited Party” has the meaning set forth in Section 3.9 (Records and Audits).

“BLA” means (a) a Biologics License Application, supplemental Biologics License Application, or similar application filed or to be filed with the FDA, as described in Title 21 of the U.S. Code of Federal Regulations, Part 601, et seq., or (b) any corresponding foreign application in another country or regulatory jurisdiction in the Territory, including, in the case of the European Union, a Marketing Approval Application filed with the EMA pursuant to the centralized approval procedure or with the applicable Regulatory Authority of a country in the European Union with respect to the mutual recognition or any other national approval procedure.

“cGMP” means the FDA’s current good manufacturing practices, as specified in 21 C.F.R. §§ 210 and 211 and the FDA’s guidance documents and all successor regulations and guidance documents thereto, and foreign equivalents thereof with respect to the European Union and Canada.

“Closing Date” means the first date on which the Company sells Series A Preferred Stock and Series A-1 Preferred Stock to its initial investors, including Amgen.

“Commercially Reasonable Efforts” means those efforts and resources commensurate with those efforts commonly used in the biopharmaceutical industry by a company of comparable size in connection with the development or commercialization of biopharmaceutical products that are of similar status, including, with respect to commercial potential, the proprietary position of the product, the regulatory status and approval process, the probable profitability of the applicable product, and other relevant factors such as technical, legal, scientific or medical factors. In determining the level of efforts constituting “Commercially Reasonable Efforts,” the following shall [*].

“Company” has the meaning set forth in the Preamble.

“Company Indemnified Parties” has the meaning set forth in Section 8.1.1 (By Amgen).

“Confidential Information” has the meaning set forth in Section 9.1.1 (Confidential Information).

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“Control” or “Controlled” means, with respect to any Know-How, material, Patent Right, or other intellectual property right, the possession (whether by ownership or license) by a Party or its Affiliates of the ability to grant to the other Party a license or access as provided herein to such Know-How, material, Patent Right, or other intellectual property right, without violating the terms of any agreement or other arrangement with any Third Party, or being obligated to pay any royalties or other consideration therefor, in existence as of the time such Party or its Affiliates would first be required hereunder to grant the other Party such license or access.

“Cover” means (a) with respect to Licensed Know-How, the Exploitation of the product would require use of such Licensed Know-How, and (b) with respect to a Patent Right, a Valid Claim would (absent a license thereunder or ownership thereof) be Infringed by the Exploitation of the product; provided that in determining whether a Valid Claim that is a claim of a pending application would be Infringed, it shall be treated as if issued as then currently prosecuted. Cognates of the word “Cover” shall have correlative meanings.

“Defending Party” has the meaning set forth in Section 4.4 (Defense of Third Party Claims).

“Diligence Notice” has the meaning set forth in Section 5.2 (Diligence).

“Disclosing Party” has the meaning set forth in Section 9.1.1 (Confidential Information).

“Dispute” has the meaning set forth in Section 10.2.1(b).

“[*] Agreement” means that certain [*] Agreement, dated as of [*], between Amgen and [*], which agreement is one of the Pre-Existing Agreements hereunder.

“EMA” means the European Medicines Agency or any successor entity thereto.

“Enforcing Party” has the meaning set forth in Section 4.3.3 (Progress Reports; Participation).

“Exploit” means to research, develop, improve, make, use, offer for sale, sell, import, export or otherwise exploit, or transfer possession of or title in, a product. Cognates of the word “Exploit” shall have correlative meanings.

“FDA” means the United States Food and Drug Administration or any successor entity thereto.

“Field” means any and all human and veterinary uses.

“First Commercial Sale” means, with respect to the Product in any country, the first sale to a Third Party for end use or consumption of the Product in such country after a BLA has been granted in such country for the Product.

“Framework Patents” means any Patent Right (other than a Licensed Patent) Controlled by Amgen or its Affiliates as of the Effective Date that: (i) has a claim that is infringed by the amino acid sequence of the Product, (ii) has a claim that is infringed by a nucleic acid sequence that encodes the amino acid sequence of the Product, or (iii) has a claim that claims Licensed Know How.

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“FTE” means the equivalent of the work of one employee full time for one year consisting of at least a total of [*] weeks or [*] hours per year (excluding vacations and holidays). No one person shall be permitted to account for more than one FTE.

“FTE Rate” means $[*] per FTE per year.

“GAAP” means the then-current generally accepted accounting principles in the United States as established by the Financial Accounting Standards Board or any successor entity or other entity generally recognized as having the right to establish such principles in the United States, in each case consistently applied. Unless otherwise defined or stated herein, financial terms shall be calculated under GAAP.

“Governmental Authority” means any court, agency, department, authority or other instrumentality of any national, state, county, city or other political subdivision.

“IND” means an Investigational New Drug Application filed with the FDA for human clinical testing of a drug or any foreign equivalent thereof.

“Indication” means the disease or condition for which an IND has been filed.

“Infringe” or “Infringement” means any infringement as determined by Law, including, without limitation, direct infringement, contributory infringement or any inducement to infringe.

“Issuing Party” has the meaning set forth in Section 9.2.2 (Review),

“Japan Agreement” means (a) the Takeda License Agreement or (b) following any termination of the Takeda License Agreement with respect to the Product, any agreement whereby the Japan Licensee has received the authorization to develop and/or commercialize the Product in Japan.

“Japan Licensee” means (a) Takeda or (b) following any termination of the Japan Agreement with respect to the Product, any Person who has rights to develop and/or commercialize the Product in Japan, including Amgen and/or its Affiliates if Amgen elects to retain any rights to develop and/or commercialize the Product in Japan.

“Know-How” means techniques, technology, trade secrets, inventions (whether patentable or not), methods, know-how, data and results (including pharmacological, toxicological and clinical data and results), analytical and quality control data and results, regulatory documents, and other information, compositions of matter, cells, cell lines, assays, animal models and other physical, biological, or chemical material.

“Law” means, individually and collectively, any and all laws, ordinances, rules, directives, administrative circulars and regulations of any kind whatsoever of any Governmental Authority within the applicable jurisdiction.

“Licensed Know-How” means all Know-How that both (a) is Controlled by Amgen and (b) was actually used by Amgen in its development of the Product at such time as Amgen last actively developed the Product prior to the Closing Date, including the Know-How set forth on the

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Licensed Know-How Schedule; provided that manufacturing process-related Know-How relating to the Product shall only be included in “Licensed Know-How” to the extent Amgen actually used such Know-How in its manufacture of the Product Lots. [*]

“Licensed Materials” means those certain materials set forth on the Licensed Materials Schedule.

“Licensed Patents” means the Patent Rights set forth on the Licensed Patents Schedule.

“Losses” has the meaning set forth in Section 8.1.1 (By Amgen).

“Marketing Approval” means all approvals, licenses, registrations or authorizations of the Regulatory Authority in a country, necessary for the manufacture, use, storage, import, marketing and sale of the Product in such country.

“Milestone Events” has the meaning set forth in Section 3.3 (Milestone Payments).

“Milestone Payments” has the meaning set forth in Section 3.3 (Milestone Payments).

“Net Sales” means the gross sales price of the Product sold by Company, its Affiliates or Sublicensee(s) (the “Selling Party”) for the sale of the Product to Third Parties, less:

(a) non-recoverable sales taxes, excise taxes, use taxes, value-added tax, and duties paid by the Selling Party in relation to the Product and any other equivalent governmental charges imposed upon the importation, use or sale of the Product (excluding taxes when assessed on income derived from sales);

(b) credits and allowances (actually allowed or paid) for defective or returned Product, including allowances for spoiled, damaged, out-dated, rejected, returned, withdrawn or recalled Product;

(c) reasonable fees paid to wholesalers, distributors, selling agents (excluding any sales representatives of a Selling Party), group purchasing organizations, Third Party payors, other contractees and managed care entities;

(d) reasonable transportation charges relating to the Product, including handling charges and insurance premiums relating thereto to the extent included as a separate entry on the invoice for such product (provided that [*] items in this clause (d) shall [*] for the relevant period);

(e) retroactive price reductions actually granted to the Third Party applicable to sales of such product;

(f) trade, cash, prompt payment and/or quantity discounts, actually allowed and taken directly by the Third Party, and mandated discounts; and

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(g) refunds, rebates, chargebacks and other allowances or payments to Governmental Authorities.

Net Sales shall be determined from books and records maintained in accordance with GAAP, consistently applied throughout the organization and across all products of the entity whose sales of Product are giving rise to Net Sales.

Where a Product is sold in combination with other therapeutically active ingredients, the Net Sales applicable to such transaction shall be calculated by multiplying the total Net Sales of such combined product by the fraction A/(A+B), where A is the actual price of the Product in the same dosage amount or quantities hi the applicable country during the applicable quarter if sold separately, and B is the sum of the actual prices of all other therapeutics with which the Product is combined, in the same dosage amount or quantities in the applicable country during the applicable quarter if sold separately. If A or B cannot be determined because values for the Product or other therapeutics with which the Product is combined are not available separately in a particular country, then Amgen and Company shall discuss an appropriate allocation for the fair market value of the Product and other therapeutics with which the Product is combined to mutually determine Net Sales for the relevant transactions based on an equitable method of determining the same that takes into account, in the Territory, variations in potency, the relative contribution of each therapeutically active ingredient, and relative value to the end user of each therapeutically active ingredient.

Net Sales shall also include, with respect to any Product sold or otherwise disposed of for any consideration other than an exclusively monetary consideration on bona fide arm’s length terms, an amount equal to the average sales price for the Product having the same dosage form and strength during the applicable reporting period in the country where such sale or other disposal occurred when the Product is sold alone and not with other products, or if the Product is not sold alone in such country during the applicable reporting period, then an amount equal to the average sales price during the applicable reporting period generally achieved for the Product having the same dosage form and strength in the rest of the Territory.

Sales of Product between or among Company and its Affiliates or Sublicensees shall be excluded from the computation of Net Sales and no payments shall be payable on such sales except where such Affiliates or Sublicensees are end users.

“Out-License” has the meaning set forth in Section 2.3 (Right of Notification).

“Out-License Fees” has the meaning set forth in Section 3.5 (Product Sublicensing Income).

“Party” has the meaning set forth in the Preamble.

“Patent Rights” means any provisional and non-provisional patents and patent applications, together with all additions, divisions, continuations, continuations-in-part, substitutions, reissues, re-examinations, issued patents, substitutes, foreign counterparts, extensions, registrations, patent term extensions, supplemental protection certificates, renewals and the like with respect to any of the foregoing.

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“Permitted CMO” means (a) a Third Party commercial manufacturing organization identified on the attached Permitted CMO Schedule (and all such Third Party’s Affiliates), as such schedule may be updated by mutual written agreement by the Parties from time to time or (b) any other party deemed to be a Permitted CMO pursuant to the terms of Section 2.4.2.

“Permitted CMO Agreement” has the meaning set forth in Section 2.4.2(a) (Transfer of Licensed Know-How and Licensed Materials).

“Permitted CMO Request” has the meaning set forth in Section 2.4.2(d) (Transfer of Licensed Know-How and Licensed Materials).

“Person” means any corporation, limited or general partnership, limited liability company, joint venture, trust, unincorporated association, governmental body, authority, bureau or agency, any other entity or body, or an individual.

“Phase 1 Clinical Trial” means any human clinical trial of the Product that satisfies the requirements of 21 C.F.R. § 312.21(a), or its successor regulation, or its non-United States equivalents, including the portion of a combination Phase 1 Clinical Trial and Phase 2 Clinical Trial that is the Phase 1 component, in accordance with the applicable protocol and as reasonably designated by Company.

“Phase 2 Clinical Trial” means any human clinical trial of the Product that satisfies the requirements of 21 C.F.R. § 312.21(b), or its successor regulation, or its non-United States equivalents, including the portion of a combination Phase 2 Clinical Trial and Phase 3 Clinical Trial that is the Phase 2 component, in accordance with the applicable protocol and as reasonably designated by Company.

“Phase 3 Clinical Trial” means any human clinical trial of the Product that satisfies the requirements of 21 C.F.R. § 312.21(c), or its successor regulation, or its non-United States equivalents, including the portion of a combination Phase 2 Clinical Trial and Phase 3 Clinical Trial that is the Phase 3 component, in accordance with the applicable protocol and as reasonably designated by Company.

“Pivotal Trial” means (a) a Phase 2 Clinical Trial, or a combination Phase 2 Clinical Trial and Phase 3 Clinical Trial, that (taken together with any other trials completed prior to or concurrently with such trial) is intended to support Marketing Approval for the Product by the relevant Regulatory Authority in the indication under study, or (b) a Phase 3 Clinical Trial.

“Pre-Existing Agreements” means those agreements listed on the Pre-Existing Agreements Schedule.

“Product” has the meaning set forth in the Recitals.

“Product Data” means all data, reports, records, materials and other Know-How that relate to Product.

“Product Lots” has the meaning set forth in Section 5.4 (Product Supply).

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“Product Technology” means the Licensed Patents and the Licensed Know-How.

“Quality Agreement” means that certain quality agreement, by and between the Parties, to be entered into as of the Closing Date and to be attached substantially in the form of hereto as the Quality Agreement Schedule.

“Receiving Party” has the meaning set forth in Section 9.1.1 (Confidential Information).

“Regulatory Authority” means any Governmental Authority or other authority responsible for granting Marketing Approvals for the Product, including the FDA, EMA and any corresponding national or regional regulatory authorities.

“Regulatory Change” has the meaning set forth in Section 5.2 (Diligence).

“Regulatory Exclusivity” means, with respect to the Product in a country, any exclusive marketing rights or data exclusivity rights conferred by the applicable Regulatory Authority in such country with respect to the Product, other than a Patent Right.

“Regulatory Filing” means any filing with any Governmental Authority with respect to the research, development, manufacture, distribution, pricing, reimbursement, marketing or sale of the Product.

“Release” has the meaning set forth in Section 9.2.2 (Review).

“Reviewing Party” has the meaning set forth in Section 9.2.2 (Review),

“Royalty Term” has the meaning set forth in Section 3.4 (Royalties).

“Sale Transaction” has the meaning set forth in Section 11.8 (Successors and Assigns).

“Selling Party” has the meaning set forth in the definition of “Net Sales”.

“Signing Date” has the meaning set forth in the Preamble.

“Specified Diligence Failure” has the meaning set forth in Section 5.2 (Diligence).

“Sublicensee(s)” means any Person other than an Affiliate of Company to which Company has granted a sublicense under this Agreement.

“Supply Agreement” means that certain supply agreement, by and between the Parties, to be entered into as of the Closing Date and to be attached substantially in the form of hereto as the Supply Agreement Schedule.

“Takeda” means Takeda Pharmaceutical Company Limited] or any successor or permitted assignee of Takeda.

“Takeda License Agreement” means that certain License Agreement, dated as of February 1, 2008, by and between Amgen and Takeda, as amended.

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“Term” has the meaning set forth in Section 10.1 (Term).

“Territory” means the entire world, excluding Japan.

“Third Party” means a Person other than (a) Amgen or any of its Affiliates and (b) Company or any of its Affiliates.

“Third Party Acquirer” has the meaning set forth in Section 11.9 (Sale Transaction or Amgen Acquisition).

“Third Party Payment” has the meaning set forth in Section 6.4 (Product Data; Regulatory).

“United States” or “U.S.” means the United States of America (including the District of Columbia).

“Valid Claim” means a claim of any issued and unexpired patent or patent application within the Licensed Patents and that has not been held invalid or unenforceable by a final decision of a court or governmental agency of competent jurisdiction, which decision can no longer be appealed or was not appealed within the time allowed; provided that if a claim of a pending patent application within the Licensed Patents [*], such claim shall not constitute a Valid Claim for the purposes of this Agreement [*].

ARTICLE 2 LICENSE GRANT; CLOSING

Section 2.1 Grant. Subject to the terms and conditions of this Agreement, commencing on the Closing Date, Amgen hereby grants to Company (a) an exclusive (even as to Amgen and its Affiliates), royalty bearing, sublicenseable (but only in accordance with Section 2.2 (Sublicenses) and Section 2.3 (Right of Notification)), license under the Licensed Patents, (b) a non-exclusive, royalty bearing, sublicenseable (but only in accordance with Section 2.2 (Sublicenses) and Section 2.3 (Right of Notification)) license under the Licensed Know-How, and (c) an exclusive (even as to Amgen and its Affiliates) license and right of reference, with the right to grant sublicenses and further rights of reference (but only in accordance with Section 2.2 (Sublicenses) and Section 2.3 (Right of Notification)), under any existing Regulatory Filings that Amgen or any of its Affiliates Controls with respect to the Product; in each case, to Exploit the Product in the Field in the Territory during the Term. Notwithstanding the foregoing, the Licensed Know-How shall be sublicenseable only in connection with the rights of Company with respect to the Product and not with respect to any other products or services.

2.1.1 Covenant Not to Xxx. In addition to the licenses set forth in this Section 2.1 (Grant) above, commencing on the Closing Date, Amgen hereby covenants not to xxx Company, its Affiliates or any Sublicensee under the Framework Patents with respect to the Exploitation of the Product in the Field in the Territory. Subject to Section 11.8 (Successors and Assigns), the Company may transfer this Covenant Not to Xxx. Amgen shall require any Amgen successor in interest to the Framework Patents to also covenant not to xxx Company, its Affiliates or any Sublicensee under the Framework Patents with respect to the Exploitation of the Product in the Field in the Territory. Should Amgen fail to secure such a covenant from a successor in interest, then immediately prior to the transfer of the Framework Patents to the successor in interest, Amgen will be deemed to have granted to Company a non-exclusive, fully paid-up, royalty-free, sublicenseable license under the Framework Patents to Exploit the Product in the Field in the Territory during the Term.

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Section 2.2 Sublicenses. Subject to compliance by Company with its obligations under Section 2.3 (Right of Notification) below, commencing on the Closing Date, the licenses granted in Section 2.1 (Grant) (including, if applicable, in the last sentence of Section 2.11 (Covenant Not to Xxx)) may be sublicensed, in full or in part, by Company to its Affiliates and Third Parties (with the right to sublicense through multiple tiers), provided that as a condition precedent to and requirement of any such sublicense:

(a) Any such permitted sublicense shall be in writing and shall be consistent with and subject to the terms and conditions of this Agreement;

(b) Company shall be responsible for any and all obligations of such Sublicensee as if such Sublicensee were “Company” hereunder; and

(c) Any such Sublicensee shall agree in writing to be bound by the substantially similar obligations of Company hereunder that are relevant to the rights sublicensed by Company to Sublicensee under such sublicense agreement, including with respect to Article 9 (Confidentiality), and Sections 2.7 (Limited Exploitation Rights), 8.1 (Indemnity), 10.2.2 (Termination for IP Challenge), and 10.5 (Effects of Termination).

Company shall provide Amgen, within [*] days following execution of each sublicense, prompt written notice thereof (which notice shall include the name of the Sublicensee and the general scope of such sublicense). Thereafter, upon Amgen’s reasonable request, Company shall provide to Amgen a copy of any such sublicense agreement executed by Company; provided that the financial terms (and any other terms Company is required to keep confidential) of any such sublicense agreement may be redacted to the extent not pertinent to an understanding of a Party’s rights or obligations under this Agreement.

Section 2.3 Right of Notification.

2.3.1 Intentionally omitted.

2.3.2 If Company’s board of directors approves the initiation of a process for the grant of a sublicense to a Third Party for development and/or commercialization of the Product (an “Out-License”), then Company shall notify Amgen in writing in advance (provided that a signed letter sent via electronic or facsimile transmission shall qualify as such written notice) and provide the intended scope (i.e., field, territory and other relevant terms) of the Out-License.

2.3.3 Upon the Completion of an Initial Public Offering (as defined in the investor rights agreement to be entered into by the Parties) or a sale of all or substantially all of Company’s assets or business, Amgen’s rights under this Section 2.3 (Right of Notification) shall terminate.

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Section 2.4 Transfer of Licensed Know-How and Licensed Materials. Amgen shall transfer to Company (or, in the case of Amgen’s transfer of the Amgen Cell Line, to the Permitted CMO) the Licensed Know-How listed on the Licensed Know-How Schedule and the Licensed Materials listed on the Licensed Materials Schedule, in accordance with a schedule to be mutually agreed by the Parties (provided such transfer must be completed within [*] after the Closing Date), and provide limited consulting support, in accordance with this Section 2.4 (Transfer of Licensed Know-How and Licensed Materials). Following the Signing Date, the Parties will in good faith reasonably cooperate to review and, if necessary, update the Licensed Know-How and Licensed Materials Schedules to correct and/or supplement such Schedules (and, as necessary, timely deliver the relevant Licensed Know-How and Materials to the Company.

2.4.1 Amgen shall provide, at its expense, consulting support (not to exceed [*] in the aggregate) in connection with such transfer and the Exploitation of the Product in the Territory during the [*] period after the Closing Date. If Company requires additional consulting support in excess of [*] in the aggregate or beyond such period after the Closing Date in connection with such transfer or the Exploitation of the Product in the Territory, then Company may request such additional support in writing. Amgen shall notify Company within [*] after receipt of such request whether it, in its sole discretion, is willing to provide such additional consulting support, which support shall be at Company’s expense, at the FTE Rate for the relevant Amgen employees.

2.4.2 With respect to Amgen’s transfer of the Amgen Cell Line, the Parties agree that the following procedures shall apply:

(a) Prior to such transfer, Company shall designate, and enter into a binding agreement with, one of the Permitted CMOs, which agreement shall provide for, among other things, (i) confidentiality and non-use provisions at least as protective as those set forth hereunder under Section 9.1 (Confidential Information) and (ii) such additional provisions as are required to comply with the manufacturing and other limitations set forth in this Section 2.4.2 (such agreement, the “Permitted CMO Agreement”). Upon Amgen’s reasonable request, Company shall provide to Amgen a copy of any such Permitted CMO Agreement (including any material amendment thereto) executed by Company; provided that the financial terms (and any other terms Company is required to keep confidential) of any such agreement may be redacted to the extent not pertinent to Amgen’s confirmation of the restrictive provisions set forth in this Section 2.4.2. Notwithstanding anything to the contrary, Company and Company’s Sublicensees are deemed Permitted CMOs, and shall not be required to enter into a Permitted CMO Agreement prior to receiving the Amgen Cell Line or conducting any manufacturing activities in connection therewith, and Amgen shall deliver such cell lines to Company and/or Company’s Sublicensees within a reasonable time following Company’s written request. For avoidance of doubt, if Company (itself, or through a third party, Affiliate, or Sublicensee) [*] (excluding any [*], but including any [*]) [*], such [*] shall [*], and the Permitted CMO restrictions set forth herein shall [*].

(b) Following Company’s and such Permitted CMG’s entry into the Permitted CMO Agreement, Amgen shall, at the direction of Company, transfer the Amgen Cell Line to the Permitted CMO to generate the Product.

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(c) Company agrees that it shall not, and it shall use its commercially reasonable efforts to cause the Permitted CMO not to: (i) reverse engineer or otherwise deconstruct the Amgen Cell Line or the initial Amgen cell culture media provided therewith, or to determine or to seek to determine information (including, but not limited to, the gene or amino acid sequence) or characteristics regarding the Amgen Cell Line or such media, other than as expressly required to manufacture the Product; (ii) clone, express, or otherwise produce any products or materials (including, without limitation, any progeny or derivatives thereof) from the Amgen Cell Line, other than as expressly permitted under this Agreement; (iii) notwithstanding anything to the contrary in Section 9.4.1 (Right to Publish), publish or otherwise publicly disclose the Amgen Cell Line; or (iv) permit any non-controlled security access to the Amgen Cell Line or otherwise transfer or provide any of the Amgen Cell Line to a Third Party or any of its Affiliates, other than as expressly required to manufacture the Product.

(d) Upon a termination or expiration of the Permitted CMO Agreement (including as a result of the appointment, with prior written notice to Amgen, by Company of a replacement Permitted CMO), the Permitted CMO shall promptly return any remaining Amgen Cell Lines and related Licensed Know-How and Licensed Materials to Amgen. If, at any time, Company desires to add a new Third Party commercial manufacturer to the Permitted CMO Schedule, it shall notify Amgen in writing (a “Permitted CMO Request”), and Amgen shall have the right, for [*] after receipt of such Permitted CMO Request, to inspect, at a reasonable time and on a reasonable basis (at Amgen’s cost), such manufacturer’s facilities to confirm its ability to fully comply with the restrictive provisions set forth in this Section 2.4.2. If Amgen rejects a Permitted CMO Request pursuant to the foregoing, it will notify Company of the reason(s) for such rejection and provide reasonable detail regarding the actions Company (or the applicable Third Party commercial manufacturer) may take to remedy such reasons for rejection. If Amgen does not reject a Permitted CMO Request within the [*] notice period, the applicable Third Party shall be deemed a Permitted CMO.

(e) Notwithstanding anything to the contrary, if, outside the scope of this Agreement, Amgen allows any Third Party commercial manufacturer access to or use of the Amgen Cell Line, such Third Party shall be deemed a Permitted CMO.

2.4.3 Company acknowledges that any materials transferred by Amgen to Company (or the Permitted CMO) under this Agreement are experimental in nature and may have unknown characteristics and therefore agrees to use prudence and reasonable care in the use, handling, storage, transportation and disposition and containment of any such materials. Accordingly, no such materials, other than the Product Lots, shall be used in any human application, including any clinical trial.

Section 2.5 Intentionally omitted.

Section 2.6 No Other Rights. Each Party acknowledges that the rights and licenses granted under this Article 2 (License Grant) and elsewhere in this Agreement are limited to the scope expressly granted. Accordingly, except for the rights expressly granted under this Agreement, no right, title, or interest of any nature whatsoever is granted whether by implication, estoppel, reliance, or otherwise, by either Party to the other Party. All rights that are not specifically granted herein are reserved.

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Section 2.7 Limited Exploitation Rights. Without limiting the provisions of Section 2.6 (No Other Rights), Company agrees (on behalf of itself and its Affiliates), and shall cause each of its Sublicensees to agree as a condition to the grant of a Sublicense, not to Exploit any Licensed Know-How or Licensed Patents in connection with any products or services other than the Product.

ARTICLE 3 FEES, ROYALTIES AND PAYMENTS

Section 3.1 Upfront Payment. Company shall pay to Amgen, within [*] after the Closing Date, a non-refundable, non-creditable upfront payment of Two Hundred Fifty Thousand Dollars ($250,000).

Section 3.2 Inventory Payment. Company shall pay to Amgen, within [*] after receipt of the two (2) Product Lots delivered pursuant to Section 5.4 (Product Supply), each of which shall meet the quality requirements for such Product Lots set forth in the Quality Agreement, a non-refundable, non-creditable inventory payment of [*] (it being agreed and understood by the Parties that no such inventory payment shall be due and payable if Amgen fails to deliver both Product Lots as contemplated hereunder).

Section 3.3 Milestone Payments. Company shall pay to Amgen certain milestone payments (“Milestone Payments”) following the first occurrence of certain milestone events, as set forth in Section 1 of the Milestones and Royalties Schedule (the “Milestone Events”). Company shall pay to Amgen the applicable Milestone Payment within [*] after the occurrence of the applicable Milestone Event. Each Milestone Payment is payable only once; except as set forth in Section 1 of the Milestones and Royalties Schedule, no Milestone Payment shall be payable for subsequent or repeated achievements of such Milestone Event. Each of the Milestone Payments shall be non-refundable and non-creditable. In the event that a Milestone Event relating to clinical development for the Product is achieved and payment that was due and payable with respect to the previous Milestone Event(s) for the Product has not been made by Company, then Company shall promptly pay Amgen such unpaid payment with respect to such previous Milestone Event(s) for the Product.

Section 3.4 Royalties. Company shall pay to Amgen on a calendar quarterly basis the tiered royalties set forth in Section 2 of the Milestones and Royalties Schedule on annual Net Sales of the Product sold by a Selling Party during the applicable Royalty Term, subject to the applicable deductions set forth in the Milestones and Royalties Schedule. Any such payment obligations accrued during a calendar quarter shall be made within [*] after the end of each such calendar quarter. Company’s obligation to pay royalties with respect to the Product in a particular country shall commence upon the First Commercial Sale of the Product in such country and shall expire on a country-by-country basis on the later of (a) the date on which the Exploitation of the Product is no longer Covered by a Valid Claim of a Licensed Patent in such country, (b) the loss of Regulatory Exclusivity for the Product in such country, and (c) the tenth (10th) anniversary of the First Commercial Sale of the Product in such country (the “Royalty Term”).

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Section 3.5 Product Sublicensing Income. Without limiting Amgen’s rights under Section 2.3 (Right of Notification) or the payment obligations set forth in Section 3.3 (Milestone Payments) and 3.4 (Royalties), in the event that, prior to [*], Company or any of its Affiliates enters into an Out-License with a Third Party under the Product Technology for development and/or commercialization of the Product, then Company shall promptly notify Amgen in writing. Within [*] after the end of a calendar month during which Company receives any Out-License Fees (as defined below), Company shall pay to Amgen [*] of (a) any amounts paid to Company or its Affiliates by such Third Party pursuant to such Out-License, whether in the form of cash, up-front fees (including any fees paid in installments), milestone payments or otherwise and (b) the fair market value of any other consideration remitted to Company by such Third Party under such Out-License ((a) and (b) collectively, “Out-License Fees”) received by Company in such calendar month, but excluding, in each case, (i) payments made to fund research and/or development work on, manufacturing of or royalties on Net Sales of the Product and (ii) the purchase of Company’s or its Affiliates’ stock (but solely to the extent that such payment is at a price equal to or less than one hundred percent (100%) of the fair market value of such stock at the date of purchase, it being understood that, for so long as [*], a stock price [*] (or, if [*]) shall be deemed to be the fair market price of such stock). To the extent such Out-License extends to technology other than the Product Technology or products other than the Product, such Out-License Fees shall be allocated between the Product Technology and the Product, on the one hand, and such other technology or products, on the other hand, on a prorated basis, based on the relative fair market values of the out-licensed technology and products. Company shall not attempt to reduce compensation rightly due to Amgen under this Section 3.5 (Product Sublicensing Income) by shifting compensation otherwise payable to Company from a Third Party with respect to the Product to another product or service for which no amounts are payable under this Section 3.5 (Product Sublicensing Income). For avoidance of doubt, any amounts paid or payable to Company in connection with the sale of all or substantially all of Company’s assets or business shall not be considered “Out-License Fees.” Notwithstanding anything else to the contrary hereunder, Company shall deduct from any amounts due under this Section 3.5 (Product Sublicensing Income) [*] of the payments paid to Amgen pursuant to Section 3.1 (Upfront Payment) and Section 3.2 (Inventory Payment).

Section 3.6 Method of Payment; Royalty Reporting. Unless otherwise agreed by the Parties, all payments due from Company to Amgen under this Agreement shall be paid in U.S. Dollars by wire transfer or electronic funds transfer of immediately available funds to an account designated by Amgen. After the First Commercial Sale of the Product and until expiration of the Royalty Term, Company shall prepare and deliver to Amgen royalty reports of the sale of the Product by the Selling Parties for each calendar quarter within [*] after the end of each such calendar quarter specifying in the aggregate and on a country-by-country basis: (a) total gross amounts for Product sold or otherwise disposed of by a Selling Party; (b) amounts deducted by category in accordance with the definition of “Net Sales” in Article I from gross amounts to calculate Net Sales; (c) Net Sales; and (d) royalties payable.

Section 3.7 Currency Conversion. In the case of sales outside the United States, payments received by Company shall be expressed in the U.S. Dollar equivalent calculated on a quarterly basis in the currency of the country of sale and converted to their U.S. Dollar equivalent using the average rate of exchange over the applicable calendar quarter to which the sales relate, in

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accordance with (a) the then-current standard methods of Company or the applicable Sublicensee, to the extent reasonable and consistently applied and (b) GAAP; provided that if, at such time, Company does not use a rate for converting into U.S. Dollar equivalents that is maintained in accordance with GAAP, then Company shall use a rate of exchange which corresponds to the rate of exchange for such currency reported in The Wall Street Journal, Internet U.S. Edition at xxx.xxx.xxx, as of the last day of the applicable reporting period (or, if unavailable on such date, the first date thereafter on which such rate is available). Company shall inform Amgen as to the specific exchange rate translation methodology used for a particular country or countries.

Section 3.8 Late Payments. In the event that any payment due hereunder that is not the subject of a good faith dispute is not made when due, the payment shall accrue interest beginning on the day following the due date thereof, calculated at the annual rate of the sum of (a) [*] plus (b) the prime interest rate quoted by The Wall Street Journal, Internet U.S. Edition at xxx.xxx.xxx on the date said payment is due, the interest being compounded on the last day of each calendar quarter; provided that in no event shall said annual interest rate exceed the maximum rate permitted by Law. Each such payment when made shall be accompanied by all interest so accrued. Said interest and the payment and acceptance thereof shall not negate or waive the right of any Party to seek any other remedy, legal or equitable, to which it may be entitled because of the delinquency of any payment including, but not limited to termination of this Agreement as set forth in Article 10 (Term and Termination).

Section 3.9 Records and Audits. Company shall keep complete and accurate records relating to the calculations of Net Sales generated in the then current calendar year and payments required under this Agreement, and during the preceding [*]. Amgen shall have the right, once annually at its own expense, to have a nationally recognized, independent, certified public accounting firm, selected by it and subject to Company’s prior written acceptance (which shall not be unreasonably withheld), review any such records of Company and its Affiliates and Sublicensees (the “Audited Party”) in the location(s) where such records are maintained by the Audited Party upon reasonable written notice (which shall be no less than [*] prior written notice) and during regular business hours and under obligations of strict confidence, for the sole purpose of verifying the basis and accuracy of payments made under Sections 3.4 (Royalties) and 3,5 (Product Sublicensing Income) within the [*] period preceding the date of the request for review. No calendar year shall be subject to audit under this Section more than once. Company shall receive a copy of each such report concurrently with receipt by Amgen. Should such inspection lead to the discovery of a discrepancy to Amgen’s detriment, Company shall, within [*] after receipt of such report from the accounting firm, pay any undisputed amount of the discrepancy together with interest at the rate set forth in Section 3.8 (Late Payments). Amgen shall pay the full cost of the review unless the underpayment of amounts due to Amgen is greater than [*] of the amount due for the entire period being examined, in which case Company shall pay the cost charged by such accounting firm for such review. Should the audit lead to the discovery of a discrepancy to Company’s detriment, Company may credit the amount of the discrepancy, without interest, against future payments payable to Amgen under this Agreement, and if there are no such payments payable, then Amgen shall pay to Company the amount of the discrepancy, without interest, within [*] after Amgen’s receipt of the report,

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Section 3.10 Taxes.

3.10.1 Sales Tax. Company is responsible for the payment of any state or local, sales or use, or similar fees or taxes arising as a result of the transfer of Licensed Materials by Amgen to Company pursuant to Section 2.4 (Transfer of Licensed Know-How and Licensed Materials) or the Product Lots pursuant to the Supply Agreement, and Company shall remit such fees or taxes to Amgen, as the collection agent, upon invoice.

3.10.2 Withholding. In the event that any Law requires Company to withhold taxes with respect to any payment to be made by Company pursuant to this Agreement, Company shall notify Amgen of such withholding requirement prior to making the payment to Amgen and provide such assistance to Amgen, including the provision of such documentation as may be required by a tax authority, as may be reasonably necessary in Amgen’s efforts to claim an exemption from or reduction of such taxes. Company shall, in accordance with such Law, withhold taxes from the amount due, remit such taxes to the appropriate tax authority, and furnish Amgen with proof of payment of such taxes within [*] following the payment. If taxes are paid to a tax authority, Company shall provide reasonable assistance to Amgen to obtain a refund of taxes withheld, or obtain a credit with respect to taxes paid.

ARTICLE 4 PATENT PROSECUTION, MAINTENANCE AND INFRINGEMENT

Section 4.1 Prosecution and Maintenance.

4.1.1 Company shall have the first right to file, prosecute and maintain all Patent Rights specified under Licensed Patents (other than in Japan), in each case at Company’s sole expense using outside counsel reasonably acceptable to Amgen. Company shall use Commercially Reasonable Efforts to prepare, file, prosecute, defend and maintain all such Patent Rights; provided that Company does not represent or warrant that any patent will issue or be granted based on patent applications contained in the Licensed Patents. Amgen shall reasonably cooperate with Company’s requests for data, affidavits, and other information and assistance to support prosecution and maintenance of such Patent Rights; provided that Company shall reimburse Amgen for its reasonable documented out-of-pocket expenses with respect to such cooperation. Company shall, at least [*] prior to submission or within [*] of receipt, forward to Amgen copies of any significant office actions, communications, and correspondence relating to the Licensed Patents. Amgen shall have the right to comment on and to discuss such prosecution and maintenance activities with Company, and Company shall consider the same in good faith.

4.1.2 As between the Parties, Amgen (or its designee) shall have the sole right to file, prosecute and maintain the Licensed Patents in Japan. Company shall not have any obligation to file, prosecute or maintain any Licensed Patents in Japan.

Section 4.2 Amgen Step-In Right. Notwithstanding the foregoing, if Company declines to file, prosecute or maintain any Patent Rights described in Section 4.1.1, elects to allow any Patent Rights described in Section 4.1.1 to lapse in any country, or elects to abandon any such Patent Rights (in each case solely to the extent contained in the Licensed Patents) before all appeals within the respective patent office have been exhausted (each, an “Abandoned Patent Right”), then:

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(a) Company shall provide Amgen with reasonable notice of such decision so as to permit Amgen to decide whether to file, prosecute or maintain such Abandoned Patent Rights and to take any necessary action (which notice shall, in any event, be given no later than [*] prior to the next deadline for any action that may be taken with respect to such Abandoned Patent Right with the U.S. Patent & Trademark Office or any foreign patent office).

(b) Amgen, at Amgen’s expense, may assume control of the filing, prosecution and/or maintenance of such Abandoned Patent Rights. The continued filing, prosecution or maintenance of such Abandoned Patent Rights shall be at Amgen’s sole discretion.

(c) Amgen shall have the right to transfer the responsibility for such filing, prosecution and maintenance of such Abandoned Patent Rights to patent counsel (outside or internal) selected by Amgen,

(d) Company shall, at Amgen’s reasonable request and expense, assist and cooperate in the filing, prosecution and maintenance of such Abandoned Patent Rights.

(e) In the event a patent issues with respect to any such Abandoned Patent Rights, Amgen shall provide reasonable notice to Company thereof and such Abandoned Patent Right shall be excluded from the license granted by Amgen to Company under Section 2.1 (Grant), unless Company (i) reimburses Amgen for its internal and external costs and expenses related to the prosecution and maintenance of such Abandoned Patent Right within [*] of issuance of any such patent and (ii) assumes, in writing, the responsibility for the continued prosecution and maintenance of such Patent Rights in accordance with the provisions of Section 4.1 (Prosecution and Maintenance).

Section 4.3 Enforcement.

4.3.1 Company Enforcement. Each Party shall notify the other promptly in writing when any Infringement by a Third Party is uncovered or reasonably suspected. Company shall have the first right to enforce any patent within the Licensed Patents (other than in Japan) against any Infringement or alleged Infringement thereof, and in each case shall at all times keep Amgen informed as to the status thereof. Company may, at its own expense, institute suit against any such infringer or alleged infringer and control, defend and settle such suit in a manner consistent with the terms and provisions hereof, and recover any damages, awards or settlements resulting therefrom, subject to Section 4.5 (Recovery). Amgen shall reasonably cooperate in any such litigation at Company’s expense; where necessary, Amgen shall join in, or be named as a necessary party to, such litigation. Company shall not enter into any settlement of any claim described in this Section 4.3.1 (Company Enforcement) that admits to the invalidity or unenforceability of the Licensed Patents, incurs any financial liability on the part of Amgen, requires an admission of liability, wrongdoing or fault on the part of Amgen, without Amgen’s prior written consent, in each case, such consent not to be unreasonably withheld.

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4.3.2 Amgen Enforcement.

(a) If Company elects not to take good faith steps to enforce any patent within the Licensed Patents described in Section4.3.1 (Company Enforcement) with respect to an Infringement (or otherwise take good faith steps to resolve such Infringement) in a particular country within [*] of receiving notice that an Infringement exists in such country (provided the foregoing shall not limit Amgen’s right to pursue equitable relief at any time in any court of competent jurisdiction in order to protect its rights in the Licensed Patents), then it shall so notify Amgen in writing, and upon receiving such notice, then Amgen may, in its sole judgment and at its own expense, take steps to enforce any such patent, including instituting suit against any such infringer or alleged infringer, and control, defend and settle such suit in a manner consistent with the terms and provisions hereof, and recover any damages, awards or settlements resulting therefrom, subject to Section 4.5 (Recovery). Company shall reasonably cooperate in any such litigation at Amgen’s expense; where necessary, Company shall join in, or be named as a necessary party to, such litigation. Amgen shall not enter into any settlement of any claim described in this Section 4.3.2(a) that admits to the invalidity or unenforceability of the Licensed Patents, incurs any financial liability on the part of Company or requires an admission of liability, wrongdoing or fault on the part of Company without Company’s prior written consent, in each case, such consent not to be unreasonably withheld.

(b) As between the Parties, Amgen (or its designee) shall have the sole right to enforce any patent within the Licensed Patents against any Infringement or alleged Infringement thereof asserted and occurring solely in Japan. Company shall reasonably cooperate in any such litigation at Amgen’s (or its designee’s) expense, including, where necessary, Company shall join in, or be named as a necessary party to, such litigation. Except for the cooperation obligations expressly set forth in this Section 4.3.2(b), Company shall not have any obligation to enforce any patent within the Licensed Patents in Japan. With respect to an Infringement or alleged Infringement of the Licensed Patents by a party that occurs both inside and outside the Territory, the Parties will meet and confer to mutually agree on a plan for enforcement (including how expenses will be shared), and each Party will reasonably cooperate in any such litigation.

4.3.3 Progress Reports; Participation. The Party initiating or defending any enforcement action described in this Section 4.3 (Enforcement) (the “Enforcing Party”) shall keep the other Party reasonably informed of the progress of any such enforcement action, and such other Party shall have the individual right to participate with counsel of its own choice at its own expense. The selection of such counsel will be subject to the Enforcing Party’s approval (which shall not be unreasonably withheld).

Section 4.4 Defense of Third Party Claims.

4.4.1 If either (a) Product Exploited by or under authority of Company becomes the subject of a Third Party’s claim or assertion of Infringement of a patent relating to the manufacture, use, sale, offer for sale or importation of the Product in the Field in the Territory, or (b) a declaratory judgment action is brought naming either Party as a defendant and alleging invalidity or unenforceability of any of the Licensed Patents (other than in Japan), the Party first having notice of the claim or assertion shall promptly notify the other Party, and the Parties shall

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promptly confer to consider the claim or assertion and the appropriate course of action. Unless the Parties otherwise agree in writing, each Party shall have the right to defend itself against a suit that names it as a defendant (the “Defending Party”). Neither Party shall enter into any settlement of any claim described in this Section 4.4.1 that admits to the invalidity or unenforceability of the Licensed Patents, incurs any financial liability on the part of the other Party, requires an admission of liability, wrongdoing or fault on the part of the other Party or, in the case that Company is the settling Party, in Amgen’s reasonable determination, conflicts with Amgen’s obligations under the Japan Agreement, without such other Party’s prior written consent, in each case, such consent not to be unreasonably withheld. In any event, the other Party shall reasonably assist the Defending Party and cooperate in any such litigation at the Defending Party’s request and expense.

4.4.2 If either (a) the Product becomes the subject of a Third Party’s claim or assertion of Infringement of a patent relating to the manufacture, use, sale, offer for sale or importation of the Product in Japan or (b) a declaratory judgment action is brought naming Amgen or Japan Licensee as a defendant and alleging invalidity or unenforceability of any of the Licensed Patents in Japan, Company shall reasonably assist Amgen or Japan Licensee, as applicable, and cooperate in any such litigation at Amgen’s or Japan Licensee’s, as applicable, request and expense.

Section 4.5 Recovery. Except as otherwise provided, the costs and expenses of the Party bringing suit under Section 4.3 (Enforcement) shall be borne by such Party, and any damages, settlements or other monetary awards recovered shall be shared as follows: (i) the amount of such recovery actually received by the Party controlling such action shall first be applied to the out-of-pocket costs of each Party in connection with such action; and then (ii) the remainder of the recovery shall be shared between the Parties as follows:

(a) If Company is the Enforcing Party, as if such recovery were Net Sales under this Agreement and Company shall pay to Amgen a portion of such Net Sales equal to the royalties calculated and payable with respect to the applicable Product under Section 3.4 (Royalties); and

(b) If Amgen is the Enforcing Party, [*] to Amgen, and [*] to Company.

Section 4.6 Patent Term Extensions and Filings for Regulatory Exclusivity Periods. Company shall advise Amgen in advance when it is considering any patent term extension or supplementary protection certificates or their equivalents for the Licensed Patents. Upon Amgen’s request, Company shall provide reasonable cooperation and assistance to Amgen (and/or its licensees) with respect to the preparation and filing of any patent term extension or supplementary protection certificates or their equivalents for the Product in Japan, With respect to any patent listings required for any Regulatory Exclusivity for the Product in the Territory, the Parties shall mutually agree on which Licensed Patents to list.

Section 4.7 Patent Marking. Company shall xxxx, and shall cause all other Selling Parties to xxxx, Product with all Licensed Patents in accordance with applicable Law, which marking obligation shall continue for as long as (and only for as long as) required under applicable Law.

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ARTICLE 5 OBLIGATIONS OF THE PARTIES

Section 5.1 Responsibility. Following the Closing Date and at all times during the Term (except as expressly stated otherwise herein), Company shall be responsible for, and shall bear all costs associated with, the research, development and commercialization of the Product in the Territory, including regulatory, pharmacovigilance, manufacturing, distribution, marketing and sales activities. Subject to Company’s obligations hereunder, all decisions concerning the development, marketing and sales of Product in the Territory, including the clinical and regulatory strategy, design, sale, price and promotion of Product covered under this Agreement, shall be within the sole discretion of Company,

Section 5.2 Diligence. Company shall (directly and/or through one or more Affiliates and/or Sublicensees or subcontractors) use Commercially Reasonable Efforts to develop and commercialize the Product in the Territory, [*]. The foregoing shall include use of Commercially Reasonable Efforts (directly and/or through one or more Affiliates and/or Sublicensees) with respect to [*]. In addition to the obligations of Company to use Commercially Reasonably Efforts, if Company, its Affiliates and/or their respective Sublicensees have not [*], Company shall promptly (but in no event later than [*] after each such applicable date) notify Amgen in writing of such failure to achieve such event (a “Specified Diligence Failure”) in a timely manner (the “Diligence Notice”); provided that, (i) if [*] requires [*], then the deadline above shall be equitably extended to account for the [*] to comply with such deadline, and (ii) if Company either (A) fails to timely [*] despite its good faith efforts to do so or (B) has a Specified Diligence Failure as a result of [*] as required under [*], then the deadline shall be equitably extended to account for [*] to comply with such deadline (provided, in the case of a failure under clause (ii)(A), such equitable extension shall [*]). Company will notify Amgen if an equitable extension pursuant to clause (ii) above is necessary, and will provide Amgen with a good faith, non-binding estimate of the expected duration of such extension. Notwithstanding anything to the contrary, Amgen shall have the right to terminate this Agreement for a Specified Diligence Failure by providing [*] written notice to Company, provided such Specific Diligence Failure is not cured during such notice period. Company shall notify Amgen immediately upon obtaining Marketing Approval of the Product in each country.

Section 5.3 Reports. On January 15 and July 15 of each year (or, on a quarterly basis if required by the Japan Licensee under the Japan Agreement), Company shall submit to Amgen a report summarizing, in reasonable detail, activities related to the Exploitation of the Product that Company or any of its Affiliates has performed, or caused to be performed, during the preceding six (6)-month period, and future activities related to the Exploitation of Product it then-currently expects to initiate during the following six (6)-month period.

Section 5.4 Product Supply.

5.4.1 On the Closing Date, the Parties shall enter into (a) the Supply Agreement, pursuant to which Amgen shall provide to Company two (2) lots of the Product drug product (each, a “Product Lot”) (provided that the second Product Lot shall only be deliverable by Amgen to the extent it meets all related quality requirements under the Supply Agreement), and (b) the Quality Agreement, with respect to such supply of the Product Lots. Except for the

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Licensed Materials listed on the Licensed Materials Schedule and such Product Lots delivered to Company, Company shall be responsible for, and shall bear the cost of, obtaining (whether by manufacturing or causing to be manufactured) research, clinical and commercial supplies of the Product. Notwithstanding anything to the contrary hereunder, as promptly as practicable after the Closing Date, Amgen will transfer the IND for the Product in the United States and Canada to Company, at Amgen’s sole cost and expense.

5.4.2 Without limiting the foregoing, Company, itself or through a Permitted CMO, shall supply to Japan Licensee clinical and commercial supplies of the Product for use, importation or sale in Japan, pursuant to the terms attached as the Clinical Supply Schedule to the Japan Agreement (with respect to clinical supply) or a supply agreement separately entered into between Company and Japan Licensee (with respect to commercial supply, but solely to the extent described in the third or fourth sentences of Section 7.3 of the Japan Agreement). Notwithstanding anything in Section 2.1 (Grant) to the contrary, Amgen hereby grants to Company all necessary rights and licenses to allow Company to comply with Company’s obligations under this Section 5.4.2.

5.4.3 Company, at the request of Amgen, shall enter into good faith negotiations with Japan Licensee for the purpose of establishing a supply agreement, quality agreement and safety agreement with respect to the Product. Under such safety agreement, Company shall (a) designate a safety liaison for communicating with Japan Licensee regarding adverse events with respect to the Product and (b) coordinate with Japan Licensee regarding any issues that may give rise to a recall.

Section 5.5 Pre-Existing Agreements. Promptly after the Closing Date, Amgen shall assign the Pre-Existing Agreements to Company (or, in the case of [*], shall [*]), to the extent it has the right under such agreement(s) to do so (and will use commercially reasonable efforts to obtain any required consents). Until the effective date of such assignment or sublicense, as applicable, (a) Company agrees to perform, or assist Amgen in performing, Amgen’s obligations (and, in the case of [*], Company agrees to [*]) under such agreement, and (b) Amgen agrees to use reasonable efforts to provide Company with any rights Amgen receives under such agreement and sublicense, as applicable.

Section 5.6 Company Location. Within sixty (60) days following the Closing Date, Company, Nina Biosciences, Inc. or Santa Xxxxx Biosciences, Inc. (either alone or together) shall establish facilities in or around Thousand Oaks, California (the “Thousand Oaks Facilities”). At least one of Company, Nina Biosciences, Inc., or Santa Xxxxx Biosciences, Inc. shall be obligated to maintain such Thousand Oaks Facilities until the earliest of (a) two (2) years following the date of such establishment, (b) the end of the Term or (c) a Sale Transaction of Company. Promptly after the Closing Date, Amgen and Company shall work together to mutually identify appropriate personnel candidates to develop and commercialize the Product in the Territory. Company shall use commercially reasonable efforts to hire and retain such candidates.

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ARTICLE 6 EX-TERRITORY ACTIVITIES

Section 6.1 Rights to the Product in Jam. Except as expressly set forth herein, the Parties acknowledge that no rights are granted hereunder to Company with respect to the Product in Japan, and that Company will have no authority or obligations with respect to the research, development, manufacture or commercialization of the Product in Japan. As between the Parties, Amgen or its licensees will have the sole right to research, develop, manufacture and commercialize the Product in Japan. Company hereby acknowledges that Amgen has previously licensed rights for the Product in Japan to Japan Licensee under the Japan Agreement. Company acknowledges that it has received and reviewed a redacted copy of the Japan Agreement.

Section 6.2 Obligations under Japan Agreement.

(a) Without limitation of Company’s obligations under Section 5.4 (Product Supply), Company agrees to perform (or assist Amgen in performing) Amgen’s obligations to Japan Licensee under the Japan Agreement, solely to the extent [*]; provided that (i) Company shall have no obligation to perform any activities which it is not permitted to perform hereunder (or for which Amgen has not granted Company the requisite rights or authority to perform), (ii) Company shall have no obligation or right to [*] under Article [*] of the Japan Agreement except to the extent [*], and (iii) in the event [*] and [*], [*]. Company shall [*] for the purpose of [*] between Company and Japan Licensee as necessary to fulfill Company’s obligations under this Section 6.2, including [*] with respect to [*] set forth in [*] of the Japan Agreement.

(b) Amgen agrees to provide Company with any relevant rights Amgen receives from Japan Licensee under the Japan Agreement (other than [*], including under [*] (but only to the extent [*], it being understood that [*]) of the Japan Agreement), to the extent [*], and Company agrees to assist Amgen in exercising such rights; provided that (i) Amgen [*] with respect to [*], including pursuant to [*]; (ii) Amgen [*] under [*] (provided that this reference to [*] shall not be deemed to [*] pursuant to Section [*] hereunder) of the Japan Agreement; (iii) the Parties shall cooperate with respect to the exercise of any right of Amgen (A) under Section [*] of the Japan Agreement or (B) to [*] under Section [*] of the Japan Agreement and the related rights under Sections [*] of the Japan Agreement (which cooperation shall include Amgen (1) [*] with respect to such exercise and (2) upon Company’s reasonable request, [*] with respect to the [*] Section [*] of the Japan Agreement in accordance with the terms thereof); and (iv) in the event [*], Amgen shall [*] under Sections [*] of the Japan Agreement.

Section 6.3 License Grant and Right of Reference. To the extent Amgen is required under the Japan Agreement to [*], Company hereby grants Amgen a license [*] as necessary for Amgen to comply with its obligations under the Japan Agreement. To the extent Amgen is required under the Japan Agreement to [*], Company hereby grants to Amgen [*] right of access and reference [*], as necessary for Amgen to comply with its obligations under the Japan Agreement.

Section 6.4 Product Data; Regulatory. Without limiting Section 6.2 (Obligations under Japan Agreement), promptly upon reasonable request by Amgen from time to time, solely for the purpose of and to the extent necessary for Amgen to comply with its obligations under the Japan

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Agreement, Company shall provide (a) to Amgen and Japan Licensee [*], copies of all the Product Data then in Company’s Control, for use in Japan, in reasonably usable electronic form and, if reasonably necessary or useful in connection with Japan Licensee’s Exploitation of the Product in Japan, original hardcopies or duplicate copies thereof; (b) to Amgen and its designee copies of all Regulatory Filings and Marketing Approvals (and all underlying data) with respect to the Product held by or on behalf of Company; (c) to Amgen and its designee (or the relevant Governmental Authority, if such provision will satisfy such Governmental Authority’s requirements) [*] and (d) reasonable cooperation to Amgen or its designee with respect to [*]. [*] shall be responsible for [*] and [*]. Notwithstanding anything to the contrary, Company shall only be obligated to provide (a)-(d) above [*] if such obligations [*]. Amgen shall [*] pursuant to fulfilling (a)-(d) above.

Section 6.5 Amendment of Japan Agreement. Any amendment to the Japan Agreement that alters Company’s obligations herein shall be subject to Company’s prior approval as follows: (i) prior to execution of any such amendment, Amgen shall provide Company with a copy of the proposed amendment and (ii) Company shall have [*] from receipt thereof to approve the proposed amendment, which approval shall not be unreasonably withheld or delayed.

ARTICLE 7 REPRESENTATIONS AND COVENANTS

Section 7.1 Mutual Warranties. Each of Amgen and Company represents and warrants that:

(a) it is duly organized and validly existing under the Law of the jurisdiction of its incorporation, and has full corporate power and authority to enter into this Agreement and to carry out the provisions hereof;

(b) it is duly authorized to execute and deliver this Agreement and to perform its obligations hereunder, and the individual executing this Agreement on its behalf has been duly authorized to do so by all requisite corporate action; and

(c) this Agreement is legally binding upon it and enforceable in accordance with its terms. The execution, delivery and performance of this Agreement by it does not conflict with any agreement, instrument or understanding, oral or written, to which it is a party or by which it may be bound, nor violate any material applicable Law.

Section 7.2 Additional Amgen Warranties. Amgen warrants to Company that:

(a) As of the Signing Date, Amgen Controls the Licensed Patents and the Licensed Know-How listed on the Licensed Know-How Schedule, and is entitled to grant the licenses specified herein. Amgen has not caused any Patent Right included in the Licensed Patents to be subject to any liens or encumbrances and Amgen has not granted to any Third Party any rights or licenses under such Patent Rights or Licensed Know-How that would conflict with the licenses granted to Company hereunder. None of the Licensed Patents are in-licensed by Amgen;

(b) As of the Signing Date, Amgen has no knowledge of any claim or litigation that has been brought or threatened in writing by any Third Party alleging that (i) the Licensed Patents are invalid or unenforceable or (ii) the manufacture, sale, offer for sale or importation of the Product in the Field in the Territory infringes or misappropriates any patents or other intellectual property rights of any Third Party;

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(c) As of the Signing Date, no patent application or registration within the Licensed Patents is the subject of any pending interference, opposition, cancellation or patent protest pursuant to 37 C.F.R. § 1.291;

(d) Amgen has made available to Company true and correct copies of the following: (i) all material Regulatory Filings for the Territory; (ii) all material correspondence with Governmental Authorities with respect to such Regulatory Filings; (iii) all minutes of any material meetings, telephone conferences or discussions with Governmental Authorities with respect to such Regulatory Filings; and (iv) all final clinical trial reports, in each case with respect to the Product and to the extent in existence as of the Signing Date;

(e) Until ownership of any Regulatory Filing is transferred to Company as set forth herein, Amgen is the owner of each such Regulatory Filing in the Field in the Territory;

(f) All the Product Lots provided to Company by Amgen pursuant to the Supply Agreement, as of the date each such Product Lot is provided to Company as set forth herein, have been manufactured, packaged, stored and labeled (as applicable) in accordance with cGMP and the specifications set forth in the Specifications Schedule;

(g) As of the Signing Date, the copy of the Japan Agreement and each Pre-Existing Agreement disclosed to Company prior to the Signing Date is, but for the redactions contained therein, a true and complete copy. Amgen further represents and warrants that Company will not be bound by any provision that is redacted from such copies of the Japan Agreement and/or any Pre-Existing Agreement;

(h) as of the Signing Date, [*], and (ii) [*]; and

(i) As of the Signing Date, Amgen has no knowledge that the manufacture of the Product using the Amgen Cell Line provided under this Agreement would infringe any patents of any Third Party.

Section 7.3 Disclaimer. EXCEPT AS OTHERWISE EXPRESSLY SET FORTH IN THIS ARTICLE 7 (REPRESENTATIONS), NEITHER PARTY MAKES ANY REPRESENTATIONS OR EXTENDS ANY WARRANTIES OF ANY KIND, EITHER EXPRESS OR IMPLIED, INCLUDING WARRANTIES OF MERCHANTABILITY, QUALITY, FITNESS FOR A PARTICULAR PURPOSE, NONINFRINGEMENT, OR VALIDITY OF PATENT CLAIMS. NOTHING IN THIS AGREEMENT SHALL BE CONSTRUED AS A REPRESENTATION MADE OR WARRANTY GIVEN BY EITHER PARTY THAT EITHER PARTY WILL BE SUCCESSFUL IN OBTAINING ANY PATENT RIGHTS, OR THAT ANY PATENTS WILL ISSUE BASED ON A PENDING APPLICATION. WITHOUT LIMITING THE RESPECTIVE RIGHTS AND OBLIGATIONS OF THE PARTIES EXPRESSLY SET FORTH HEREIN, EACH PARTY SPECIFICALLY DISCLAIMS ANY GUARANTEE THAT THE PRODUCT WILL BE SUCCESSFUL, IN WHOLE OR IN PART.

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Section 7.4 Company Covenants. Company covenants to Amgen that:

(a) it will conduct, and will cause its Affiliates and contractors to conduct, all preclinical and clinical studies for Product and manufacturing of Product, in accordance with (i) all U.S. Laws and the Laws of the country in which such clinical studies are conducted, (ii) the known or published standards of the FDA and the Regulatory Authority in such country, and (iii) the scientific standards applicable to the conduct of such studies and activities in the United States and in such country including current good laboratory practice, current good clinical practice and current good manufacturing practice. Neither Company, nor any officer, employee or agent of Company, will make an untrue statement of a material fact to any Regulatory Authority with respect to Product (whether in any submission to such Regulatory Authority or otherwise), and none of the foregoing will knowingly fail to disclose a material fact required to be disclosed to any Regulatory Authority with respect to Product;

(b) it will, and will cause its Affiliates and contractors to, comply with all Law with respect to the commercialization of Product;

(c) it will not knowingly employ any personnel or knowingly use a contractor or consultant that has been debarred by the FDA (or subject to a similar sanction of any other Regulatory Authority), or that is subject of an FDA debarment investigation or proceeding (or similar proceeding of any other Regulatory Authority); and

(d) it shall comply with all (i) U.S. Laws prohibiting the re-export, directly or indirectly, of certain controlled U.S.-origin items without a license to parties located in certain countries or appearing on certain U.S. Government lists of restricted parties; (ii) U.S. Laws prohibiting participation in non-U.S. boycotts that the United States does not support; and (iii) U.S. Laws prohibiting the sale of products to parties from any country subject to U.S. economic sanctions or who are identified on related U.S. Government lists of restricted parties.

ARTICLE 8 INDEMNIFICATION

Section 8.1 Indemnity.

8.1.1 By Amgen. Amgen agrees to defend Company and its (and its Affiliates’) directors, officers, employees and agents (the “Company Indemnified Parties”) at Amgen’s cost and expense, and will indemnify and hold Company and the other Company Indemnified Parties harmless from and against any claims, losses, costs, damages, fees or expenses (including legal fees and expenses) (collectively, “Losses”) to the extent resulting from any Third Party claim (including product liability claims) arising out of or otherwise relating to (a) the gross negligence or willful misconduct of Amgen, (b) the material breach of this Agreement or the representations and warranties made hereunder by Amgen, (c) the Exploitation of the Product by or on behalf of Amgen (or the Exploitation of the Product by Japan Licensee), or (d) the death or injury of a person caused by the failure of the Product Lots delivered to Company hereunder to be manufactured in compliance with cGMP or the specifications set forth on the Specifications Schedule; except, in each case, to the extent such Losses result from clause (a), (b), or (c) of Section 8.1.2 (By Company). In the event of any such claim against the Company Indemnified

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Parties by a Third Party, the foregoing indemnity obligations shall be conditioned upon (x) Company promptly notifying Amgen in writing of the claim, (y) Company granting Amgen sole management and control, at Amgen’s sole expense, of the defense of the claim and/or its settlement (provided that Amgen shall not settle any such claim without the prior written consent of Company if such settlement does not include a complete release from liability or if such settlement would involve undertaking an obligation (including the payment of money by a Company Indemnified Party), would bind or impair a Company Indemnified Party, or includes any admission of wrongdoing or that any intellectual property or proprietary right of Company is invalid or unenforceable), and (z) at Amgen’s expense, the Company Indemnified Parties cooperating with Amgen; provided that in the case of (x) and (z) any failure or delay in such notice or cooperation shall not excuse any obligations of Amgen except to the extent Amgen is actually prejudiced thereby, The Company Indemnified Parties may, at their option and expense, be represented in any such action or proceeding by counsel of their own choosing.

8.1.2 By Company. Company agrees to defend Amgen and its (and its Affiliates’) directors, officers, employees and agents (the “Amgen Indemnified Parties”) at Company’s cost and expense, and will indemnify and hold Amgen and the other Amgen Indemnified Parties harmless from and against any Losses resulting from any Third Party claim (including product liability claims) to the extent arising out of or otherwise relating to (a) the gross negligence or willful misconduct of Company, its Affiliates, or their respective Sublicensees, (b) the material breach of this Agreement or the representations, warranties and covenants made hereunder by Company, or (c) the Exploitation of the Product by or on behalf of Company, its Affiliates, or their respective Sublicensees (including from product liability and intellectual property infringement claims); except, in each case, to the extent such Losses result from clause (a), (b), (c) or (d) of Section 8.1.1 (By Amgen), In the event of any such claim against the Amgen Indemnified Parties by a Third Party, the foregoing indemnity obligations shall be conditioned upon (x) Amgen promptly notifying Company in writing of the claim, (y) Amgen granting Company sole management and control, at Company’s sole expense, of the defense of the claim and/or its settlement (provided that Company shall not settle any such claim without the prior written consent of Amgen if such settlement does not include a complete release from liability or if such settlement would involve undertaking an obligation (including the payment of money by an Amgen Indemnified Party), would bind or impair an Amgen Indemnified Party, or includes any admission of wrongdoing or that any intellectual property or proprietary right of Amgen is invalid or unenforceable) and (z) at Company’s expense, the Amgen Indemnified Parties cooperating with Company; provided that in the case of (x) and (z) any failure or delay in such notice or cooperation shall not excuse any obligations of Company except to the extent Company is actually prejudiced thereby. The Amgen Indemnified Parties may, at their option and expense, be represented in any such action or proceeding by counsel of their own choosing.

Section 8.2 LIMITATION OF DAMAGES. IN NO EVENT SHALL EITHER PARTY BE LIABLE HEREUNDER TO THE OTHER PARTY FOR ANY PUNITIVE, RELIANCE, INDIRECT, SPECIAL, INCIDENTAL OR CONSEQUENTIAL DAMAGES (INCLUDING LOST REVENUE, LOST PROFITS, OR LOST SAVINGS) HOWEVER CAUSED AND UNDER ANY THEORY, EVEN IF IT HAS NOTICE OF THE POSSIBILITY OF SUCH DAMAGES. THE LIMITATIONS SET FORTH IN THIS SECTION 8.2 (LIMITATION OF DAMAGES) SHALL NOT APPLY WITH RESPECT TO (A) ANY BREACH OF ARTICLE 9

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(CONFIDENTIALITY) OR (B) THE INTENTIONAL MISCONDUCT OF A PARTY. NOTHING IN THIS SECTION 8.2 (LIMITATION OF DAMAGES) IS INTENDED TO LIMIT OR RESTRICT THE INDEMNIFICATION RIGHTS OR OBLIGATIONS OF A PARTY UNDER THIS ARTICLE 8 (INDEMNIFICATION) WITH RESPECT TO ANY DAMAGES PAID BY THE OTHER PARTY TO A THIRD PARTY IN CONNECTION WITH A THIRD-PARTY CLAIM.

Section 8.3 Insurance. At least [*] prior to [*], Company shall at its own expense procure and maintain during the Term (and for [*] thereafter) [*] insurance coverage adequate to cover its obligations hereunder and which is/are consistent with normal business practices of prudent pharmaceutical companies. Additionally, at least [*] prior to [*], Company shall at its own expense procure and maintain during the Term (and for [*] thereafter) [*] insurance coverage adequate to cover its obligations hereunder and which is consistent with normal business practices of prudent pharmaceutical companies. Each insurance policy required by and procured by Company under this Section 8.3 (Insurance) shall [*]. Such insurance shall not be construed to create a limit of Company’s liability with respect to its indemnification obligations under this Article 8 (Indemnification). Company shall provide Amgen with a certificate of insurance or other evidence of such insurance, upon request. Company shall provide Amgen with written notice at least [*] prior to the cancellation, non-renewal or a material change of or in such insurance which materially adversely affects the rights of Amgen hereunder, and [*] prior written notice of cancellation for non-payment of premiums. Company’s insurance hereunder shall be primary with respect to the obligations for which Company is liable hereunder.

ARTICLE 9 CONFIDENTIALITY

Section 9.1 Confidential Information.

9.1.1 Confidential Information. Each Party (“Disclosing Party”) may disclose to the other Party (“Receiving Party”), and Receiving Party may acquire during the course and conduct of activities under this Agreement, certain proprietary or confidential information of Disclosing Party in connection with this Agreement. The term “Confidential Information” means (a) all Licensed Know-How, (b) all Licensed Materials, and (c) all ideas and information of any kind, whether in written, oral, graphical, machine-readable or other form, whether or not marked as confidential or proprietary, which are transferred, disclosed or made available by Disclosing Party or at the request of Receiving Party. During the Term, Amgen shall keep completely confidential all Licensed Know-How and Licensed Materials to the extent disclosure of such Confidential Information would negatively impact in any material way the Exploitation of the Product in the Territory by Company or its Affiliates or Sublicensees. For clarity, any modifications, improvements, enhancements, derivatives, or extracts of or related to the Licensed Know-How and Licensed Materials conceived or reduced to practice by or on behalf of Company, its Affiliates, or Sublicensees shall be considered Company’s Confidential Information.

9.1.2 Restrictions. During the Term and for [*] thereafter, Receiving Party shall keep completely confidential all Disclosing Party’s Confidential Information. Receiving Party shall not use Disclosing Party’s Confidential Information except to the extent necessary to perform its

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obligations and exercise its rights under this Agreement [*]. Receiving Party has the right to disclose Disclosing Party’s Confidential Information without Disclosing Party’s prior written consent, to the extent and only to the extent reasonably necessary, to Receiving Party’s Affiliates and their employees, subcontractors, consultants or agents who have a need to know such Confidential Information in order to perform its obligations and exercise its rights under this Agreement and who are required to comply with the restrictions on use and disclosure in this Section 9.1.2 (Restrictions). Receiving Party shall use diligent efforts to cause those entities and persons to comply with the restrictions on use and disclosure in this Section 9.1,2 (Restrictions). Receiving Party assumes responsibility for those entities and persons maintaining Disclosing Party’s Confidential Information in confidence and using same only for the purposes described herein.

9.1.3 Exceptions. Receiving Party’s obligation of nondisclosure and the limitations upon the right to use the Disclosing Party’s Confidential Information shall not apply to the extent that Receiving Party can demonstrate that the Disclosing Party’s Confidential Information: (a) was known to Receiving Party or any of its Affiliates prior to the time of disclosure, as evidenced by contemporaneous written records; (b) is or becomes public knowledge through no fault or omission of Receiving Party or any of its Affiliates; (c) is obtained by Receiving Party or any of its Affiliates from a Third Party under no obligation of confidentiality to Disclosing Party; or (d) has been independently developed by employees, subcontractors, consultants or agents of Receiving Party or any of its Affiliates without the aid, application or use of Disclosing Party’s Confidential Information, as evidenced by contemporaneous written records.

9.1.4 Permitted Disclosures. Receiving Party may disclose Disclosing Party’s Confidential Information to the extent (and only to the extent) such disclosure is reasonably necessary in the following instances:

(a) in order to comply with applicable law (including any securities law or regulation or the rules of a securities exchange) or with a legal or administrative proceeding;

(b) in connection with prosecuting or defending litigation, Marketing Approvals and other regulatory filings and communications, and filing, prosecuting and enforcing Patents in connection with Receiving Party’s rights and obligations pursuant to this Agreement; and

(c) in connection with exercising its rights hereunder, to its Affiliates; potential and future collaborators (including Sublicensees where Company is the Receiving Party); permitted and potential acquirers or assignees; potential investment bankers, investors and lenders; and, where Amgen is the Receiving Party, Japan Licensee;

provided that (1) with respect to the foregoing clause (a) or (b), where reasonably possible, Receiving Party shall notify Disclosing Party of Receiving Party’s intent to make any disclosure pursuant thereto sufficiently prior to making such disclosure so as to allow Disclosing Party adequate time to take whatever action it may deem appropriate to protect the confidentiality of the information to be disclosed, and (2) with respect to the foregoing clause (c), each of those named people and entities are required to comply with the restrictions on use and disclosure in Section 9.1.2 (Restrictions) (other than investment bankers, investors and lenders, which must be bound prior to disclosure by commercially reasonable obligations of confidentiality).

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Section 9.2 Terms of this Agreement; Publicity.

9.2.1 Restrictions. The Parties agree that the terms of this Agreement shall be treated as Confidential Information of both Parties, and thus may be disclosed only as permitted by Section 9.1.4 (Permitted Disclosures). Except as required by law and except for the press release attached hereto as the Press Release Schedule to be issued on or after the Closing Date, each Party agrees not to issue any press release or public statement disclosing information relating to this Agreement or the Product in the Territory or the transactions contemplated hereby or the terms hereof without the prior written consent of the other Party not to be unreasonably withheld (or as such consent may be obtained in accordance with Section 9.2.2 (Review)).

9.2.2 Review. In the event either Party (the “Issuing Party”) desires to issue a press release or other public statement disclosing information relating to this Agreement or the transactions contemplated hereby or the terms hereof, the Issuing Party shall provide the other Party (the “Reviewing Party”) with a copy of the proposed press release or public statement (the “Release”). The Issuing Party shall specify with each such Release, taking into account the urgency of the matter being disclosed, a reasonable period of time within which the Receiving Party may provide any comments on such Release (but in no event less than [*] business days) and if the Receiving Party fails to provide any comments during the response period called for by the Issuing Party, the Reviewing Party shall be deemed to have consented to the issuance of such Release. If the Receiving Party provides any comments, the Parties shall consult on such Release and work in good faith to prepare a mutually acceptable Release. Either Party may subsequently publicly disclose any information previously contained in any Release so consented to. For the avoidance of doubt, notwithstanding anything to the contrary, Company, in its sole discretion, may (a) subject to the terms of Section 9.1 (Confidential Information), disclose information relating to Company’s, its Affiliates’, and Sublicensees’ activities in connection with the subject matter hereunder, including information relating to research and any clinical trial conducted by Company (including in marketing or publicity materials) and any health or safety matter related to the Product and (b) disclose information relating to this Agreement or the transactions contemplated hereby to current and potential investors in and potential acquirers and Sublicensees of Company who are bound prior to disclosure by commercially reasonable obligations of confidentiality.

Section 9.3 Relationship to the Confidentiality Agreement. All “Confidential Information” disclosed or received by or on behalf of a Party under that certain Confidential Disclosure Agreement between Amgen and Xxxxxxx Xxxxxxx Xxxxxxxx & Xxxxx, dated October 17, 2011, shall be deemed “Confidential Information” hereunder and shall be subject to the terms and conditions of this Agreement.

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Section 9.4 Publications.

9.4.1 Right to Publish.

(a) Subject to the provisions of Sections 9.1 (Confidential Information), 9.2 (Terms of this Agreement; Publicity) and 9.4.2 (Review), both Parties shall have the right to publish with respect to the Product in publications based in the Territory, and to make scientific presentations on the Product in the Territory (provided that prior to any such publication or presentation by Amgen with respect to the Product in the Territory, Amgen shall obtain Company’s prior written consent). Neither Party shall publish the [*] or information concerning the [*] without the prior consent of the other Party.

(b) As between the Parties, Amgen shall have the sole right to publish with respect to the Product in publications based outside the Territory and to make scientific presentations on the Product outside the Territory. Upon Amgen’s request, Company shall meet with Japan Licensee to formulate a global publication strategy for the Product in good faith. In addition, (i) Company shall not present or publish in the Territory data generated outside the Territory by or on behalf of Amgen’s licensee or Amgen without Amgen’s prior written consent and (ii) Amgen shall not present or publish outside the Territory data generated inside the Territory by or on behalf of Company or its Sublicensees without Company’s prior written consent.

9.4.2 Review. Except as required by Law or court order, for any proposed publication or presentation regarding the Product in the Territory, the Party desiring to make such publication: (a) shall transmit a copy of the proposed publication for review and comment to the other Party and any applicable licensee) at least [*] days prior to the submission of such publication to a Third Party; (b) shall postpone such publication for up to an additional [*] days upon request of a Party (or applicable licensee) to allow the consideration of appropriate patent applications or other protection to be filed; (c) upon request of the other Party (or applicable licensee) shall remove all Confidential Information of the other Party (or applicable licensee); and (d) shall consider all reasonable comments made by the other Party (or applicable licensee).

ARTICLE 10 TERM AND TERMINATION

Section 10.1 Term. The term of this Agreement (the “Term”) shall commence on the Signing Date, and unless terminated earlier as provided in this Article 10 (Term and Termination), shall continue in full force and effect until expiration of the last-to-expire Royalty Term for the Product in the Territory. Upon expiration of this Agreement, the licenses granted to Company by Amgen under this Agreement to Exploit the Product shall be fully paid-up, royalty-free, irrevocable and non-exclusive.

Section 10.2 Termination by Amgen.

10.2.1 Breach.

(a) Subject to Section 10.2.1(b), Amgen shall have the right to terminate this Agreement in full upon delivery of written notice to Company in the event of any material breach by Company of any terms and conditions of this Agreement; provided that such termination shall not be effective if such breach has been cured within [*] after written notice thereof is given by Amgen to Company specifying the nature of the alleged breach.

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(b) Notwithstanding the foregoing, in the event of a good faith dispute between the Parties as to whether Company has materially breached any terms or conditions of this Agreement (a “Dispute”), then, except [*], (i) the Parties shall resolve the Dispute pursuant to Section 11.4 (Governing Law; Jurisdiction) (the period until the resolution of such Dispute being the “Dispute Period”); (ii) each Party will continue to perform its obligations under this Agreement during the Dispute Period and (iii) if the relevant judicial finder of fact (“Finder of Fact”) determines that Company is in material breach as asserted by Amgen (a “Breach”), then, following such adjudication by the Finder of Fact and in lieu of any such termination by Amgen, Company shall have the right to cure (A) any payment breach by payment in full of any finally determined monetary award and (B) any other breach that [*]. For avoidance of doubt, this Section 10.2.1 shall not abrogate Amgen’s right to obtain injunctive or equitable relief at any time from a court of competent jurisdiction and/or attorneys’ fees in connection with any relief so granted.

10.2.2 Termination for IP Challenge. To the extent allowed by Law, Amgen shall have the right, upon written notice to Company, to terminate in full (a) this Agreement, in the event that Company or any of its Affiliates directly challenges in a legal or administrative proceeding the patentability, enforceability or validity of any Licensed Patents or Framework Patents, or (b) any Sublicensee’s sublicense, in the event that such Sublicensee directly challenges in a legal or administrative proceeding the patentability, enforceability or validity of any Licensed Patents; provided that Amgen shall not have the right to terminate any sublicense under Section 10.2.2 (b) (Termination for IP Challenge) for any such challenge by any Sublicensee if such challenge is dismissed within [*] days of Amgen’s notice to Company under this Section 10.2.2 (Termination for IP Challenge) and not thereafter continued.

Section 10.3 Termination by Company.

10.3.1 Breach. Company shall have the right to terminate this Agreement in full upon delivery of written notice to Amgen in the event of any material breach by Amgen of any terms and conditions of this Agreement; provided that such termination shall not be effective if such breach has been cured within [*] days after written notice thereof is given by Company to Amgen specifying the nature of the alleged breach.

10.3.2 Discretionary Termination. Company shall have the right to terminate this Agreement in full [*] days after delivery of written notice to Amgen if the Board of Directors of Company concludes due to scientific, technical, regulatory or commercial reasons, including (a) safety or efficacy concerns, including adverse events of the Product, (b) concerns relating to the present or future marketability or profitability of the Product, (c) reasons related to patent coverage or (d) existing and anticipated competition, renders the Exploitation of the Product no longer commercially practicable for Company.

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Section 10.4 Termination Upon Bankruptcy. Either Party may terminate this Agreement if, at any time, the other Party shall (a) file in any court or agency pursuant to any statute or regulation of any state, country or jurisdiction, a petition in bankruptcy or insolvency or for reorganization or for an arrangement or for the appointment of a receiver or trustee of that Party or of its assets, (b) propose a written agreement of composition or extension of its debts, (c) be served with an involuntary petition against it, filed in any insolvency proceeding, and such petition has not been dismissed within [*] days after the filing thereof, (d) propose or be a party to any dissolution or liquidation, (e) make an assignment for the benefit of its creditors or (f) admit in writing its inability generally to meet its obligations as they fall due in the general course.

Section 10.5 Effects of Termination. Upon termination by either Party under Sections 10.2 (Termination by Amgen), 10.3 (Termination by Company) or 10.4 (Termination Upon Bankruptcy):

(a) Company shall responsibly wind-down, in accordance with accepted pharmaceutical industry norms and ethical practices, any on-going clinical studies for the Product for which it has responsibility hereunder in which patient dosing has commenced or, if reasonably practicable and requested by Amgen, Company, its Affiliates or its Sublicensees shall complete such trials. Company shall be responsible for any costs associated with such wind-down. Amgen shall pay all costs incurred by either Party to complete such studies should Amgen request that such studies be completed.

(b) A termination of this Agreement shall [*] with respect to the Product pursuant to Section [*]; provided that, with respect to [*], as of the effective date of termination and [*] consistent with the terms and conditions contained herein, with [*], or [*], Company may, to the extent it is legally permitted to do so, [*] and [*] and [*] and [*].

(c) All rights and licenses granted by Amgen to Company in Article 2 (License Grant) with respect to the Product shall terminate, and Company and its Affiliates shall cease all use of Licensed Know-How and Licensed Patents related to the Product and all Exploitation of the Product, except to the extent required under Section 10.5(a).

(d) Upon Amgen’s request, all Marketing Approvals and other regulatory filings and communications relating to the Product owned (in whole or in part) or otherwise controlled by Company and its Affiliates and Sublicensees, and all other documents relating to or necessary to further Exploit any Product, as such items exist as of the effective date of such termination (including all related completed and ongoing clinical studies) shall be assigned to Amgen, and Company shall provide to Amgen one (1) copy of the foregoing and all documents contained in or referenced in any such items, together with the raw and summarized data for any clinical studies (and where reasonably available, electronic copies thereof). In the event of any failure to obtain assignment, Company hereby consents and grants to Amgen the right to access and reference (without any further action required on the part of Company, whose authorization to file this consent with any Regulatory Authority is hereby granted) any such item.

(e) Company hereby grants to Amgen and its Affiliates, and Amgen and its Affiliates shall automatically have, a [*] license, [*], under Know-How and Patent Rights that are Controlled by Company or any of its Affiliates and Sublicensees for Exploiting the Product and any improvement to any of the foregoing (such license effective only as of and after the effective date of such termination). The Patent Rights so licensed shall be subject to [*].

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(f) Upon Amgen’s request, Company shall assign (or, if applicable, shall cause its Affiliates or Sublicensees to assign) to Amgen all of Company’s (and such Affiliates’ and Sublicensees’) right, title and interest in and to any registered or unregistered trademarks or internet domain names worldwide that are specific to a Product (it being understood that the foregoing shall not include any trademarks or internet domain names that contain the corporate or business name(s) of Company).

(g) Company agrees (and shall cause its Affiliates and Sublicensees as a condition of the grant of the applicable Sublicense to so agree) to fully cooperate with Amgen and its designee(s) to facilitate a smooth, orderly and prompt transition of the Exploitation of Product in the Territory to Amgen and/or its designee(s). Upon request by Amgen, and at Amgen’s expense, Company shall transfer to Amgen some or all quantities of the Product in its possession. If Company is, at the time of such termination of this Agreement, party to any Third Party contracts with respect to the Product, then it shall provide Amgen notice and (to the extent permitted to do so) copies thereof. Company shall assign to Amgen (and Amgen shall assume and perform) any such contracts requested by Amgen, to the extent it has the right under such contract(s) to do so (and shall use commercially reasonable efforts to obtain any required consents). In addition, Company shall, at Amgen’s cost and expense, provide any cooperation reasonably requested by Amgen to ensure uninterrupted supply of the Product, If Company manufactured the Product at the time of termination, then Company shall continue to provide for manufacturing of such Product for Amgen, at [*] of the fully-burdened manufacturing cost therefor (for clarity, such cost will be paid by Amgen to Company), from the date of notice of such termination until the sooner to occur of (a) such time as Amgen is able, using commercially reasonable efforts to do so, to secure an acceptable alternative commercial manufacturing source from which sufficient quantities of Product may be procured and legally sold in the Territory and (b) [*] from the effective date of termination of this Agreement.

Company shall duly execute and deliver, or caused to be duly executed and delivered, such instruments and shall do and cause to be done such activities and things, including the filings of such assignments, agreements, documents and instruments, as may be necessary under, or as Amgen may reasonably request in connection with, Amgen’s rights under this Section 10.5 (Effects of Termination).

Section 10.6 Survival. In addition to the termination consequences set forth in Section 10.5 (Effects of Termination), the following provisions shall survive termination or expiration of this Agreement: Articles 1 (Definitions), 7 (Indemnification), 8 (Confidentiality), and 10 (Miscellaneous) and Sections 2.7 (Limited Exploitation Rights), 3.3 (Milestone Payments) (with respect to milestones reached prior to such expiration or termination), 3.4 (Royalties) (with respect to sales made before such expiration or termination), 3.5 (Product Sublicensing Income) through 3.10 (Taxes) (inclusive) (with respect to periods with sales of Products made before such expiration or termination), 4.3 (Enforcement) through 4.5 (Recovery) (with respect to any action initiated prior to such expiration or termination), 7.3 (Disclaimer), 10.5 (Effects of Termination) and this Section 10.6 (Survival). Termination or expiration of this Agreement shall not relieve

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the Parties of any liability or obligation which accrued hereunder prior to the effective date of such termination or expiration nor preclude either Party from pursuing all rights and remedies it may have hereunder or at law or in equity with respect to any breach of this Agreement nor prejudice either Party’s right to obtain performance of any obligation. All other rights and obligations shall terminate upon expiration of this Agreement.

ARTICLE 11 MISCELLANEOUS

Section 11.1 Entire Agreement; Amendment. This Agreement and all Schedules attached to this Agreement constitute the entire agreement between the Parties as to the subject matter hereof. All prior and contemporaneous negotiations, representations, warranties, agreements, statements, promises and understandings with respect to the subject matter of this Agreement are superseded hereby. Neither Party shall be bound by or charged with any written or oral agreements, representations, warranties, statements, promises or understandings not specifically set forth in this Agreement. No amendment, supplement or other modification to any provision of this Agreement shall be binding unless in writing and signed by both Parties.

Section 11.2 Section 365(n) of the Bankruptcy Code. All rights and licenses granted under or pursuant to any section of this Agreement are, and shall otherwise be deemed to be, for purposes of Section 365(n) of the U.S. Bankruptcy Code, licenses of rights to “intellectual property” as defined under Section 101(35A) of the U.S. Bankruptcy Code to the extent permitted thereunder. The Parties shall retain and may fully exercise all of their respective rights and elections under the U.S. Bankruptcy Code or any analogous provisions in any other country or jurisdiction. Upon the commencement of a bankruptcy proceeding by or against either Party, the Party that is not a party to such proceeding shall further be entitled to a complete duplicate of (or complete access to, as appropriate) any such intellectual property and all embodiments of such intellectual property, which, if not already in the non-subject Party’s possession, shall be promptly delivered to it, unless the Party subject to the proceeding elects to continue, and continues, to perform all of its obligations under this Agreement.

Section 11.3 Independent Contractors. The relationship between Company and Amgen created by this Agreement is solely that of independent contractors. This Agreement does not create any agency, distributorship, employee-employer, partnership, joint venture or similar business relationship between the Parties. Neither Party is a legal representative of the other Party, and neither Party can assume or create any obligation, representation, warranty or guarantee, express or implied, on behalf of the other Party for any purpose whatsoever. Each Party shall use its own discretion and shall have complete and authoritative control over its employees and the details of performing its obligations under this Agreement.

Section 11.4 Governing Law; Jurisdiction. This Agreement and its effect are subject to and shall be construed and enforced in accordance with the law of [*], without regard to its conflicts or choice of law rules or principles, except as to any issue which depends upon the validity, scope or enforceability of any Licensed Patent, which issue shall be determined in accordance with the laws of the country in which such patent was issued. Each of the Parties hereby irrevocably and unconditionally consents to submit to the exclusive jurisdiction of the courts of [*] for any matter arising out of or relating to this Agreement and the transactions contemplated

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hereby, and agrees not to commence any litigation relating thereto except in such courts. Each of the Parties hereby irrevocably and unconditionally waives any objection to the laying of venue of any matter arising out of this Agreement or the transactions contemplated hereby in the courts of [*] and hereby further irrevocably and unconditionally waives and agrees not to plead or claim in any such court that any such matter brought in any such court has been brought in an inconvenient forum. The Parties agree that a final judgment in any such matter shall be conclusive and may be enforced in other jurisdictions by suits on the judgment or in any other manner provided by law. Any proceeding brought by either Party under this Agreement shall be exclusively conducted in the English language.

Section 11.5 Notice. Except as otherwise expressly set forth herein, all notices or communication required or permitted to be given by either Party hereunder shall be deemed sufficiently given if mailed by registered mail or certified mail, return receipt requested, or sent by overnight courier, such as Federal Express, to the other Party at its respective address set forth below or to such other address as one Party shall give notice of to the other from time to time hereunder. Mailed notices shall be deemed to be received on the third (3rd) business day following the date of mailing. Notices sent by overnight courier shall be deemed received the following business day.

If to Company:

Pinta Biosciences, Inc.

c/o Kleiner Xxxxxxx Xxxxxxxx & Xxxxx

0000 Xxxx Xxxx Xxxx

Xxxxx Xxxx, XX 00000

Attn: Xxxxx Xxxxxxxxxxx, MD

If to Amgen:

Amgen Inc.

Xxx Xxxxx Xxxxxx Xxxxx

Xxxxxxxx Xxxx, XX 00000

Attn: Corporate Secretary

Section 11.6 Compliance With Law; Severability. Nothing in this Agreement shall be construed to require the commission of any act contrary to Law. If any one or more provisions of this Agreement is held to be invalid, illegal or unenforceable, the affected provisions of this Agreement shall be curtailed and limited only to the extent necessary to bring it within the applicable legal requirements, and the validity, legality and enforceability of the remaining provisions of this Agreement shall not in any way be affected or impaired thereby.

Section 11.7 Non-Use of Names. Amgen shall not, and shall require its Affiliates not to, use the name, trademark, logo or physical likeness of Company or any of its officers, directors or employees, or any adaptation of any of them, in any advertising, promotional or sales literature, without such Company’s prior written consent. Company shall not, and shall require its Affiliates not to, use the name, trademark, logo or physical likeness of Amgen or any of its officers, directors or employees, or any adaptation of any of them, in any advertising, promotional or sales literature, without Amgen’s prior written consent.

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Section 11.8 Successors and Assigns. Neither this Agreement nor any of the rights or obligations created herein, except for the right to receive any remuneration hereunder, may be assigned by either Party, in whole or in part, without the prior written consent of the other Party, not to be unreasonably withheld or delayed except that either Party shall be free to assign this Agreement in connection with any merger, sale of such Party or sale of all or substantially all of the assets of the Party relating to this Agreement (a “Sale Transaction”), without the prior consent of the non-assigning Party; provided that, in the case of a Sale Transaction of Company, the assignee shall be required to assume all of Company’s obligations hereunder. This Agreement shall bind and inure to the benefit of the successors and permitted assigns of the Parties hereto. Any assignment of this Agreement in contravention of this Section 11.8 (Successors and Assigns) shall be null and void.

Section 11.9 Sale Transaction or Amgen Acquisition. In the event of (x) a Sale Transaction, or (y) the acquisition by Amgen of all or substantially all of the business of a Third Party (together with any entities that were Affiliates of such Third Party immediately prior to such acquisition, an “Amgen Acquiree”), whether by merger, sale of stock, sale of assets or otherwise (an “Amgen Acquisition”), the intellectual property rights of the acquiring party in a Sale Transaction, if other than one of the Parties to this Agreement (together with any entities that were affiliates of such Third Party immediately prior to such Sale Transaction, a “Third Party Acquirer”), or the Amgen Acquiree, as applicable, shall not be included in the technology licensed hereunder or otherwise subject to this Agreement.

Section 11.10 Waivers. A Party’s consent to or waiver, express or implied, of the other Party’s breach of its obligations hereunder shall not be deemed to be or construed as a consent to or waiver of any other breach of the same or any other obligations of such breaching Party. A Party’s failure to complain of any act, or failure to act, by the other Party, to declare the other Party in default, to insist upon the strict performance of any obligation or condition of this Agreement or to exercise any right or remedy consequent upon a breach thereof, no matter how long such failure continues, shall not constitute a waiver by such Party of its rights hereunder, of any such breach, or of any other obligation or condition. A Party’s consent in any one instance shall not limit or waive the necessity to obtain such Party’s consent in any future instance and in any event no consent or waiver shall be effective for any purpose hereunder unless such consent or waiver is in writing and signed by the Party granting such consent or waiver.

Section 11.11 No Third Party Beneficiaries. Except as expressly provided with respect to Amgen Indemnified Parties and Company Indemnified Parties in Article 8 (Indemnification) and Amgen’s licensees, including Japan Licensee, nothing in this Agreement shall be construed as giving any Person, other than the Parties hereto and their successors and permitted assigns, any right, remedy or claim under or in respect of this Agreement or any provision hereof.

Section 11.12 Headings; Schedules. Article and Section headings used herein are for convenient reference only, and are not a part of this Agreement. All Schedules are incorporated herein by this reference.

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Section 11.13 Interpretation. Except where the context otherwise requires, wherever used, the singular shall include the plural and the plural the singular, the use of any gender shall be applicable to all genders and the word “or” is used in the inclusive sense (and/or). The term “including” as used herein shall mean including, without limiting the generality of any description preceding such term. All references to a “business day” or “business days” in this Agreement means any day other than a day which is a Saturday or Sunday or any day banks are authorized or required to be closed in the United States. The language in all parts of this Agreement shall be deemed to be the language mutually chosen by the Parties. The Parties and their counsel have cooperated in the drafting and preparation of this Agreement, and this Agreement therefore shall not be construed against any Party by virtue of its role as the drafter thereof.

Section 11.14 Counterparts. This Agreement may be executed in counterparts by a single Party, each of which when taken together shall constitute one and the same agreement, and may be executed through the use of facsimiles or electronically transmitted documents.

[Signature page follows]

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IN WITNESS WHEREOF, the Parties have executed this Agreement as of the date first set forth above.


PINTA BIOSCIENCES, INC.		AMGEN INC.

By:	/s/ Xxxxx Xxxxxxxxxxx	By:	/s/ Xxxxxxxx Xxxxxxx
Name:	Xxxxx Xxxxxxxxxxx	Name:	Xxxxxxxx Xxxxxxx
Title:	President	Title:	Executive Vice President and Chief Finance Officer

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Schedule

Quality Agreement

QUALITY AGREEMENT

Between

[Name of Company]

Hereafter referred to as “COMPANY”

and

AMGEN Inc.

Hereafter referred to as “AMGEN”

This Quality Agreement is intended by the Parties to set forth a plan for the quality assurance groups of AMGEN and COMPANY to work in relation to the manufacture, labeling, testing, release, shipping and storage of the Product (as defined below). By signing below, the respective quality assurance representatives acknowledge and agree to the provisions of this Quality Agreement.


Agreed and accepted for:		Agreed and accepted for:

[NAME OF COMPANY]		AMGEN

By:		By:

Printed Name:		Printed Name:

Title:		Title:

Date:		Date:

Table of Contents

TABLE OF CONTENTS


		Page
1.	BACKGROUND INFORMATION		2
2.	SCOPE		2
3.	DEFINITIONS		2
4.	RESPONSIBILITIES		4
5.	COMMUNICATION		5
6.	BATCH DISPOSITION (PRODUCT RELEASE)		5
7.	QUALITY CONTROL/TESTING		5
8.	REFERENCE SAMPLES		6
9.	RETENTION SAMPLES		6
10.	LABELAPPROVAL		6
11.	RECEIVING. SHIPPING, STORAGE AND DESTRUCTION		7
12.	CHANGE CONTROL		7
13.	INVESTIGATIONS OF NONCONFORMANCES, DISCREPANCIES (POST DISTRIBUTION NC’S)		8
14.	VISITS, AUDITS AND INSPECTIONS		8
15.	DISPUTE RESOLUTION		9
16.	CUSTOMER COMPLAINTS		9
17.	REPROCESSING AND REWORK		9
18.	RECALLS AND VOLUNTARY WITHDRAWALS		9
19.	RESPONSIBLE PERSONS: CONTACT INFORMATION		10
20.	GENERAL		10
EXIIIBIT A			11

EXHIBIT B			12

EXHIBIT C			13

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1.	BACKGROUND INFORMATION

1.1

AMGEN Inc. (hereinafter referred to as “AMGEN”) and [Company Name] (hereinafter referred to as “COMPANY”) (hereinafter referred to individually as “Party” or collectively as “Patties”) have entered into an Exclusive License Agreement (the “License Agreement”), dated as of [ ], 2012, and a Supply Agreement (the “Supply Agreement”), dated as of [ ], 2012, regarding AMG 745 (the “Product”) for clinical use. This Quality Agreement provides the quality requirements as specified under Section 5.4 of the License Agreement and Section2.1 of the Supply Agreement.

1.1.1

This Quality Agreement defines the quality obligations of the Parties and their respective affiliates or approved contractors, with respect to the manufacture, labeling, testing, release, and delivery of Product in accordance with the License Agreement and Supply Agreement and the quality aspects of such Product.

SCOPE

2.1

The provisions of this Quality Agreement supplement the provisions of the License Agreement and Supply Agreement. The terms of the License Agreement and Supply Agreement shall remain in full force and effect. In the event of any conflict between the License Agreement, or Supply Agreement, and this Quality Agreement, the License Agreement and Supply Agreement shall govern over the conflict.

2.2

This Quality Agreement may be amended only by mutual written agreement of the Parties.

2.3

Exhibits to this Quality Agreement are intended to provide additional definition to the applicable topic and, as such, should be updated to reflect the current information and business process, as applicable. Amendment of the Exhibits does not require re-approval of the Quality Agreement unless the Quality Agreement itself is affected. Exhibits and all amendments of Exhibits shall be approved by mutual written agreement of the Parties.

2.4

All activities under this Quality Agreement shall be performed in compliance with cGMP regulations.

2.5

This Quality Agreement shall expire at the termination, cancellation, or expiration, as the case may be, of the License Agreement.

3.	DEFINITIONS

3.1

All capitalized terms not otherwise defined in this Quality Agreement shall have the definition set forth in the License Agreement and/or Supply Agreement.

3.2

As used in this Quality Agreement, the following terms shall have the following meanings:


Certificate of Analysis (CoA)		CoA prepared for Product representing the analytical results for the material, the accuracy of which has been certified by AMGEN. This is an approved record provided by AMGEN for a given batch containing the analytical test results required by the specification for the material.

Certificate of Compliance (CoC)		CoC (or QADS) prepared by AMGEN for the Product representing that the Product was manufactured according to cGMP requirements.

Disposition Manager		AMGEN Quality Assurance staff member qualified to perform the comprehensive quality assessment and make the disposition decision for a specific batch of Product.

Disposition Package		Documentation set provided to COMPANY representing AMGEN batch disposition of the Product. Documents comprising the Disposition Package are provided in Exhibit B.

Drug Substance		Shall have the meaning given in the Supply Agreement.

Drug Product		The finished dosage form of AMG745 in labeled vials delivered in accordance with License Agreement and the Supply Agreement.

Final Release		Release of Product for distribution by COMPANY in accordance with COMPANY standard operating procedures (“SOPs”).

cGMP		All applicable laws and regulations relating to current Good Manufacturing Practices, as promulgated by the United States Food and Drug Administration (FDA), and foreign equivalents thereof as promulgated by the applicable Regulatory Authority in the European Union or Canada.

Disposition Package		Documentation set provided to COMPANY representing AMGEN batch disposition of the Product. Documents comprising the Disposition Package are provided in Exhibit B.

Manufacturer’s Release		Release of Product by AMGEN, according to AMGEN’s procedures and cGMP regulations.

Manufacturing Information Schedule		The information listed under the heading “Manufacturing Information” in the Licensed Know-How Schedule attached to the License Agreement.

Material Change		A material change to the Specifications or the manufacturing process for Product, or any other material changes to the Product including the analytical methods that AMGEN uses that support performance of its obligations under the License Agreement or Supply Agreement.

Nonconformance		Deviations incurred during the manufacture, testing, or storage of the Product prior to delivery to COMPANY, which were determined by AMGEN procedures to potentially impact the safety, identity, strength, potency, or quality of the Product.

Out of Specification (OOS)		An examination, measurement or test result that does not conform with pre-established specification requirements established by the relevant Party.


Product		The Drug Substance and Drug Product manufactured by AMGEN.

Quality Assurance Disposition (QAD)		A document containing the disposition decision for a specific batch of Product.

Qualified Person		Qualified Person, as defined in 2001/83 EC and 2001/20 EC; responsible for (QP) certification of any Product batch prior to its use in a European clinical study.

Recall		A “recall” or “market withdrawal” (each as defined per Section 7.3 of Title 21 (Food and Drugs) of the Code of Federal Regulations, or, with respect to a jurisdiction other than the United States, the equivalent regulations of the applicable Regulatory Authority in such jurisdiction) of Product or any lots thereof.

Reference Sample		Sample collected from the manufacture of Product for the purpose of being analyzed, should the need arise, to support significant investigations.

Regulatory Authority		Any government administrative agency, commission or other governmental authority, body or instrumentality, or any federal, state, local, domestic or foreign governmental regulatory body.

Reprocessing		Reprocessing shall mean introducing an intermediate or active pharmaceutical ingredient, including one that does not conform to standards or specifications, back into the process and repeating a step (e.g., filtration) that is part of the established manufacturing process.

Retention Samples		A fully packaged unit from a batch of Drug Product. It is stored for identification purposes.

Rework		Rework shall mean subjecting an intermediate that does not conform to one or more processing steps that are different from the established manufacturing process to obtain acceptable quality intermediate or Product.

Specifications		AMGEN approved set of analytical methods, requirements, and acceptance criteria as used to judge the identity, purity and potency of all source materials, raw materials, and fmished filled Product which comprises the material, as referenced in the Specifications Schedule.

Specifications Schedule		The Specifications Schedule attached to the License Agreement.

4.	RESPONSIBILITIES

4.1

Without limiting any other provision of this Quality Agreement, the Parties agree that this Quality Agreement is intended to carry out the following guiding principles:

4.1.1

The Parties’ quality obligations with respect to the manufacture, labeling, testing, release, and delivery of Product are as set forth in this Quality Agreement.

4.1.1.1

The Parties acknowledge that AMGEN shall have the right to perform responsibilities hereunder through its Affiliates (as defined in the License Agreement) and contractors.

5.	COMMUNICATION

5.1

AMGEN and COMPANY agree to provide verbal communication to one another, in a timely manner, as necessary or appropriate for a given issue. Both Parties also agree to follow-up and clarify promptly in writing those important verbal communications to ensure clarity of issues.

5.2

Routine verbal and written communications required herein shall be delivered to the individuals indicated in EXHIBIT A or their delegates.

5.3

Each Party must notify the other in writing of any (potential) theft, counterfeits and illegal diversion of Product manufactured by AMGEN within twenty-four (24) hours upon awareness of such events.

6.	BATCH DISPOSITION (PRODUCT RELEASE)

6.1

AMGEN Quality Responsibility

6.1.1

AMGEN shall be responsible for the Manufacturer’s Release of the material to COMPANY.

6.1.2

AMGEN shall provide to COMPANY the Disposition Package for each batch of material supplied to COMPANY, upon shipment. The documents to be included in the Disposition Package are provided in Exhibit B.

6.2

COMPANY Quality Responsibility

6.2.1

COMPANY shall be solely responsible for the Final Release of the Product for distribution within the Territory.

6.2.2

COMPANY shall be deemed to have conclusively and fully accepted the Product unless COMPANY notifies AMGEN in writing of any claim to the effect that the Product received did not meet the Specifications and/or cGMP requirements, within thirty (30) days of receipt.

6.2.3

A QP authorized by COMPANY will be responsible for certification of Product for use in clinical trials in the European Union, according to the requirements set out in the European Union cGMPs.

7.	QUALITY CONTROL/TESTING

7.1

Transfer and Qualification of Analytical Testing

7.1.1

The provisions of this Section 7 supplement the terms of the License Agreement and Supply Agreement relating to the know-how and scientific and technical information needed for compliance of the Product in the United States, Canada and/or the European Union.

7.1.2

Refer to the Manufacturing Information Schedule for the transfer of analytical methods from AMGEN to COMPANY.

7.1.3

As part of such transfer, AMGEN shall provide COMPANY with reference standard and non-commercial critical reagents and supporting documentation in accordance with AMGEN policies and procedures. Refer to the Manufacturing Information Schedule for the transfers of reference standard and non-commercial critical reagents.

7.2

AMGEN Testing Responsibility

7.2.1

AMGEN will conduct testing of Product according to Specifications, methods, policies and procedures as approved by AMGEN. AMGEN shall provide the Specifications to COMPANY per the Manufacturing Information Schedule.

7.2.2

Stability Testing

7.2.2.1

AMGEN will continue the initiated stability studies of the Product per the AMGEN Stability program and provide data updates as set forth in the Manufacturing Information Schedule. As soon as practical, AMGEN will notify COMPANY of any confirmed stability failure of the Product and provide periodic updates on the OOS investigation.

7.2.2.2

AMGEN will be responsible for assigning a Product expiration date per AMGEN’s Stability program requirements.

7.3

COMPANY Testing Responsibility

7.3.1

Batch release documents will be evaluated by COMPANY upon receipt for conformance to Specifications and applicable cGMP requirements. COMPANY will not be performing additional testing to the AMGEN released batches.

8.	REFERENCE SAMPLES

8.1

AMGEN shall retain Reference Samples for each manufactured batch of Product released to COMPANY per AMGEN established procedures.

8.2

The amount of samples collected will be in compliance with AMGEN policies and procedures and applicable Law.

9.	RETENTION SAMPLES

9.1

COMPANY is responsible for retaining Retention Samples for each packaged batch of Product released for clinical distribution per established COMPANY procedures and applicable Law.

10.	LABELAPPROVAL

10.1

Label Creation and Application

10.1.1

AMGEN will be responsible for labeling of Product that will be distributed to COMPANY according to AMGEN procedures. The label will include the following information: cautionary statement, Amgen artwork number, manufacturing date and drug product batch number.

11.	RECEIVING. SHIPPING, STORAGE and DESTRUCTION

11.1

AMGEN shall make Product available for shipment to COMPANY in an appropriate manner that will assure the stability of the Product during shipment, using defined, qualified packaging configurations.

11.2

AMGEN shall ship labeled Product to COMPANY per AMGEN policies and procedures.

11.3

Upon receipt, COMPANY is responsible for reviewing tracking data, inspecting security seals and labels for evidence of tamper, and performing reconciliation of Product upon receipt of shipment per COMPANY procedures. COMPANY shall notify AMGEN within two (2) business days of becoming aware of any discrepancies.

11.3.1.1

AMGEN and COMPANY will jointly investigate any discrepancies within AMGEN’s defined quality systems.

11.4

COMPANY is responsible for reviewing shipping data such as temperature recording data and storage conditions upon receipt of shipment.

11.5

COMPANY is responsible for adequate storage of the Product upon receipt according to the storage requirements specified in the Specifications.

11.6

COMPANY shall be responsible for the destruction of any unused Product and material in accordance with applicable Law.

11.7

Unused cGMP materials including excipients, raw material, primary packaging components, product contacting material (e.g. resin) will be destroyed and reconciled by AMGEN per AMGEN procedures.

12.	CHANGE CONTROL

12.1

Changes by AMGEN

12.1.1

AMGEN shall notify COMPANY of AMGEN’s intention to implement any Material Change. The notification of such Material Change and the details of such Material Change shall be provided to COMPANY by AMGEN according to EXHIBIT C.

12.1.1.1

COMPANY’s QA will respond to such notification for a Material Change within two (2) business days of receipt.

12.2

Notwithstanding anything to the contrary in this Section 12, AMGEN shall have the right to immediately make any change required to protect patient safety or as required by applicable Law and shall give COMPANY prompt written notice thereof.

13.	INVESTIGATIONS OF NONCONFORMANCES, DISCREPANCIES (POST DISTRIBUTION NC’S)

13.1

If a Nonconformance, as solely determined by AMGEN, is identified after a Product batch has been shipped to COMPANY, AMGEN shall inform COMPANY as soon as reasonably possible of such Nonconformance.

13.2

AMGEN will provide support, as necessary and reasonable, to enable COMPANY to comply with applicable regulatory reporting requirements that may result from the occurrence of Nonconformances.

14.	VISITS, AUDITS AND INSPECTIONS

14.1

Person-in-Plants

14.1.1

Neither Party shall have the right to have a person-in-plant in the other Party’s facilities to observe operations and documentations.

14.2

For Cause Audit by COMPANY

14.2.1.1

Upon the request of COMPANY and approval by AMGEN, AMGEN shall permit COMPANY to conduct a “For Cause” audit during the Term in the case of a quality or regulatory event, which events may include recall of Product in the Territory.

14.2.1.2

Such “For Cause” audits require prior written request by COMPANY and shall be conducted during normal AMGEN business hours. The scope, agenda, and timeline for such audit must be approved by AMGEN prior to conducting the audit. The written notification must clearly state the scope of the audit and regulatory standards to be used to conduct the audit.

14.2.2

Audit Findings

14.2.2.1

At COMPANY’s or AMGEN’s request, an exit meeting shall be held with COMPANY and its representatives and AMGEN and its representatives to discuss audit findings, if any. COMPANY shall provide AMGEN with a copy of the audit report within thirty (30) calendar days upon completion of the audit. For those findings that AMGEN determines in good faith may materially affect AMGEN’s ability to perform the Services, AMGEN shall issue a written response to COMPANY’s report within thirty (30) days of AMGEN’s receipt of such report. AMGEN’s response shall identify the timelines and approach for addressing COMPANY’s findings.

14.3

Regulatory Agency Inspections

14.3.1

COMPANY shall notify AMGEN within twenty-four (24) hours upon notification by any Regulatory Authority of any intended inspection of AMGEN’s facilities or records relating to the manufacturing, testing, and storage of the Product.

14.3.2

AMGEN will be solely responsible for hosting and managing regulatory inspections at its facilities.

14.3.3

COMPANY will have the right to review and comment on AMGEN’s proposed response to observations raised by the Regulatory Authorities relating to the Product and AMGEN shall consider such comments in good faith. AMGEN shall provide COMPANY with a copy of the final response after submission to any Regulatory Authorities.

14.3.4

AMGEN will inform COMPANY of any critical Regulatory Authority inspection observations not directly relevant to the Product where it can reasonably be assumed the observation impacts upon the Services or Product provided to COMPANY.

15.	DISPUTE RESOLUTION

15.1

Disputes relating to non-compliance or nonconformance of Product with the Specifications shall be governed by the terms set forth in Section 11.4 of the License Agreement.

16.	CUSTOMER COMPLAINTS

16.1

COMPANY shall notify AMGEN of any complaints related to the manufacturing processes of the Product supplied by AMGEN that reasonably require an investigation under applicable Law or current practices within one (1) business day after COMPANY first becomes aware of such information.

16.2

COMPANY will use commercially reasonable efforts to provide AMGEN with information and complaint samples, or if such samples are not available, images of defects in Product, including a reasonable failure description, in order to permit proper and timely complaint investigation specifically for the corresponding defect. Upon receipt of COMPANY’s investigation request, AMGEN shall perform an investigation into the root cause of the problem according to AMGEN’s policies and procedures, and provide an investigation update within forty-five (45) calendar days following receipt of such notification.

16.3

Complaint investigation requests and results shall be directly communicated between COMPANY and AMGEN complaint representatives. A list of contacts shall be provided to each Party and updated in writing by each Party within a reasonable period of time after any Party changes its contact(s).

17.	REPROCESSING AND REWORK

17.1

AMGEN will not conduct any Reprocessing or Reworking of materials of Product without prior approval by COMPANY.

18.	RECALLS AND VOLUNTARY WITHDRAWALS

18.1

COMPANY shall have the sole right to control a Recall of the Product in the Field in the Territory; provided that COMPANY shall not take any action with respect to any Recall in the Field in the Territory without first notifying AMGEN and meeting (in person, by telephone or otherwise, as mutually agreed) with

AMGEN (and, if so requested by AMGEN, Japan Licensee) to discuss the circumstances of such potential Recall and to consider appropriate courses of action provided that the foregoing shall not limit COMPANY’s obligations in relation to Recalls under any applicable Law and COMPANY shall be entitled to take action in relation to a Recall without first notifying AMGEN where it considers such action is reasonably necessary to be taken in a time-frame that does not reasonably permit such notification (in which case it shall provide such notification promptly thereafter). COMPANY shall maintain complete and accurate records of any such Recall for such periods as may be required by Law, but in any event for no less than fifteen (15) years. AMGEN (and its licensees) shall have the sole right to control the handling of any Recall in Japan.

19.	RESPONSIBLE PERSONS: CONTACT INFORMATION

19.1

The individuals listed in EXHIBIT A shall be the key points of contact between AMGEN and COMPANY relating to the rights and obligations of the Parties in this Quality Agreement.

20.

GENERAL

20.1

The provisions of Sections 11.3 through 11.8 (inclusive) and 11.10 through 11.14 (inclusive) of the License Agreement are incorporated herein by reference and apply hereto mutatis mutandis.

10.

EXHIBIT A

Responsible Persons and Contact Information


COMPANY
Name	Email Address	Contact Number	Responsibility

Exhibit A Version Date:


Agreed and accepted for:		Agreed and accepted for:

[COMPANY NAME]		AMGEN

By:		By:

Printed Name:		Printed Name:

Title:		Title:

Date:		Date:

-11-

EXHIBIT B

AMGEN Disposition Package

The following documents are to comprise the AMGEN Disposition Package to support the release of each Product batch to COMPANY:


General		Nonconformance List and Summary for cell banking, Drug Substance and Drug Product (Report includes only lot-tied nonconformances deemed by AMGEN to have a potential impact of the safety, identity, strength, potency, or quality of the Product, according to established AMGEN procedures.
Drug substance manufacture		Core batch documentation for each clinical batch, including Expansion/cell culture Harvest Purification Preparation of UF/DF buffers Formulation and Final Filtration CoC/QAD, CoA

Drug Product Manufacture		Batch documentation for each clinical batch, including Sterile filtration Filling Capping and Inspection CoC,CoA

Exhibit B Version Date:


Agreed and accepted for:		Agreed and accepted for:

(COMPANY NAME]		AMGEN

By:		By:

Printed Name:		Printed Name:

Title:		Title:

Date:		Date:

-12-

EXHIBITC

Change Control Business Process

SOP-013477, Amgen’s Partner Change Notification Process, governs the process by which AMGEN identifies and notifies COMPANY of changes as required per the Quality Agreement. This procedure leverages AMGEN’s existing change control.

AMGEN Quality point of contact is responsible for screening changes for impact to COMPANY, notifying COMPANY of the change and recording COMPANY’s assessment in AMGEN’s change control management system. COMPANY is notified by the AMGEN Quality point of contact of a change through the use of a controlled form FORM-022482, Change Notification. The Change Notification will provide COMPANY with all relevant information regarding the proposed change thereby allowing COMPANY to fully assess the change and the impact of the change to COMPANY, including any applicable Product regulatory filing(s). COMPANY must provide a response to the change using this same form within two (2) business days from the date of receipt by COMPANY of such notification.

Exhibit C Version Date:


Agreed and accepted for:		Agreed and accepted for:

(COMPANY NAME]		AMGEN

By:		By:

Printed Name:		Printed Name:

Title:		Title:

Date:		Date:

-13-

Schedule

Supply Agreement

SUPPLY AGREEMENT

This SUPPLY AGREEMENT (“Supply Agreement”) is made and entered into as of [ ], 2012 (“Effective Date”) by and between Amgen Inc., a corporation organized under the laws of the State of Delaware having an address at Xxx Xxxxx Xxxxxx Xxxxx, Xxxxxxxx Xxxx, Xxxxxxxxxx 00000-0000, X.X.X. (“Amgen”), and Pinta Biosciences, Inc., a Delaware corporation having an address at [ ] (“Company”). Amgen and Company are sometimes referred to herein individually as a “Party” and collectively as the “Parties”.

RECITALS

WHEREAS, Amgen and Company have entered into that certain Exclusive License Agreement dated as of September 7, 2012 pursuant to which Amgen grants certain licenses to Company for the development, manufacture and commercialization of the Product (as defined therein) (the “License Agreement”); and

WHEREAS, in connection with the License Agreement, Company desires to procure from Amgen, and Amgen is willing to perform for Company, certain transitional fill/finish services relating to AMG 745 (as more fully described herein), on the terms and conditions hereof.

NOW, THEREFORE, in consideration of the premises and the mutual promises and covenants contained in this Supply Agreement, and for other good and valuable consideration, the receipt and sufficiency of which are hereby acknowledge, the Parties agree as follows:

1. DEFINITIONS

The following defined terms are used in this Supply Agreement and shall have the meanings set forth below. Capitalized terms used but not defined in this Supply Agreement shall have the meanings ascribed to them in the License Agreement.

“Batch” means a single lot of Finished Drug Product.

“Company Proprietary Technology” means all Technology and rights thereto relating to the Finished Drug Product that are transferred to Company pursuant to the License Agreement or that are thereafter owned, developed, or controlled by Company and that Company in turn provides to Amgen hereunder during the Term of this Supply Agreement.

“Delivery” (or Deliver or other variants thereof) means completion of in-process release testing by Amgen and the availability of Finished Drug Product for shipment pursuant to Section 3.2.

“Delivery Date” means a date stated in the Services Schedule for which Delivery of Finished Drug Product is expressly specified.

“Disposition” (or Dispose or other variants thereof) means either the rejection or acceptance of a Batch, or part thereof, by the applicable quality assurance department of Amgen.

-15-

“Drug Substance” means the substance or mixture of substances intended to be used in the manufacture of AMG 745 and that, when used in the production of AMG 745, becomes an active pharmaceutical ingredient of AMG 745.

“Facility” means Amgen’s facilities located in Thousand Oaks, California.

“Finished Drug Product” means Drug Substance that has been Processed by Amgen pursuant to this Supply Agreement and that meets the Specifications.

“Intellectual Property Rights” means any and all now known or hereafter existing: (i) rights associated with works of authorship, including copyrights and moral rights; (ii) trade secret rights; (iii) patent rights and industrial property rights; (iv) other proprietary rights in Technology of every kind and nature; and (v) all registrations, applications, renewals, and extensions of the foregoing, in each case in any jurisdiction throughout the world.

“Processing” means, with respect to Drug Substance, to filter, formulate, sterile filter, aseptically fill, lyophilize (if applicable), inspect and/or Disposition to form Finished Drug Product all in accordance with cGMP and the Specifications. “Process” and “Processed” shall have comparable meanings.

“Quality Agreement” means that certain agreement entitled “Quality Agreement” entered into by and between Company and Amgen and dated as of the date hereof, as such may be amended from time to time.

“Services” means the Processing tasks, functions and other responsibilities and activities specifically set forth in the Services Schedule.

“Specifications” means the written requirements for the Finished Drug Product which are attached as the Specifications Schedule to the License Agreement.

“Subcontractor” means a person or entity that has been retained by Amgen pursuant to the terms of this Supply Agreement to perform a portion of Amgen’s obligations hereunder.

“Technology” means all inventions (whether or not patentable), discoveries, know-how, tradesecrets, methods, processes, techniques, confidential information, specifications, protocols, schematics, diagrams, reagents, compounds, samples, formulations, data, databases, works of authorship, and other forms of technology.

“Term” means the period of time during which this Supply Agreement is in effect in accordance herewith.

2. TERMS REGARDING SERVICES.

2.1 Services. During the Term and subject to the terms and conditions of this Supply Agreement, Amgen shall, or shall cause one or more of its Affiliates or Subcontractors to, perform the Services in accordance with cGMP for the purpose of Processing the Drug Substance for Company to produce and store Finished Drug Product. Amgen shall perform quality control and quality assurance testing consistent with cGMP as set out in the Quality

Agreement. The Parties agree that the Quality Agreement shall set forth the responsibilities of the Parties with respect to quality and regulatory aspects of the Services hereunder. Pending Processing of the Drug Substance into Finished Drug Product, Amgen shall store such Drug Substance on behalf of Company in accordance with the Specifications.

2.2 Cooperation and Coordination. The Parties shall cooperate with each other in all matters relating to the provision and receipt of the Services. Company and Amgen shall each appoint an authorized representative (each, a “Coordinator”) for the exchange of all communications, other than legal notices, related to the Services. The name and title of the initial Coordinators shall be provided in writing. Each Party may replace its Coordinator at any time for any reason by providing written notice to the other Party.

2.3 Transitional Nature of the Services.

(i) Acknowledgement. Company acknowledges and agrees that (a) the Services provided hereunder are transitional in nature and are furnished by Amgen solely in connection with the transactions contemplated by the License Agreement; (b) Amgen does not routinely provide such Services to third parties; and (c) Amgen has no interest in continuing the provision of any of the Services after expiration of the Term. Company and Amgen expressly acknowledge and agree that the obligation of Amgen to provide transitional services under this Supply Agreement to Company following the Effective Date is limited to the Services set forth in the Services Schedule, and, except as specifically provided in the License Agreement, there exists no obligation on the part of Amgen to provide any other transitional or other services to Company following the Effective Date.

(ii) Transition Covenant. Company shall (a) timely perform the obligations of Company set forth in this Supply Agreement in support of the Services and, with the assistance of Amgen as provided in the License Agreement, timely complete the transition of the Services to Company or a third party on Company’s behalf at the expiration of the Term; and (b) take all such action reasonably requested by Amgen or as otherwise reasonably necessary to facilitate, support and encourage the timely completion of the Services and transition the Services at the expiration of the Term to Company’s internal organization, to one or more contract manufacturing organizations, or to one or more other third party suppliers acting on Company’s behalf all as provided in the License Agreement.

3. TITLE, SHIPMENT, AND RISK OF LOSS.

3.1 Title. As between Amgen and Company, upon receipt of payment by Amgen from Company under Section 3.2 of the License Agreement, Company shall hold title to the Finished Drug Product.

3.2 Shipment of Finished Drug Product. Amgen and Company shall meet the Delivery Date requirements agreed to by the Parties as set forth in the Services Schedule. All Finished Drug Product shall be shipped to Company or its designee EXW (Ex Works) (as defined in Incoterms 2010) Amgen’s Facility. Company shall establish and maintain an account with a mutually acceptable carrier for purposes of shipping Finished Drug Product from Amgen to Company or its designee. Company shall be responsible for shipping and transportation costs. Risk of loss or damage to Finished Drug Product shall transfer to Company when made available to Company for pickup at Amgen’s Facility warehouse.

4. TERM AND TERMINATION.

4.1 Term. The term of this Agreement shall commence on the Effective Date and shall, unless terminated earlier in accordance with this Article 4, expire on completion in full of the Services.

4.2 Suspension of Services. Amgen’s obligations to perform the Services shall be automatically suspended if Company is in breach of any material covenant, warranty or obligation hereunder or under the License Agreement, until Company has cured such breach. This Supply Agreement shall automatically terminate upon the termination of the License Agreement.

4.3 Survival. In addition to any provision of this Supply Agreement that expressly survives the termination of this Supply Agreement, the provisions of Sections 2.3, 4.2 and 4.3 and Articles 1, 5, 6, 7, 9 and 10 shall survive the termination of this Agreement. All other provisions of this Agreement shall terminate and be of no further effect upon the termination of this Agreement for any reason.

5. REPRESENTATIONS AND WARRANTIES.

5.1 Representations and Warranties by Company. Company represents and warrants to Amgen as follows:

(i)

Finished Drug Product supplied by Amgen under this Supply Agreement that is covered by the license granted under the License Agreement shall be used solely in accordance with the License Agreement; and

(ii)

Company shall comply with all Laws, including all importation and export control laws, if applicable.

5.2 Disclaimer. EXCEPT AS EXPRESSLY PROVIDED IN THE LICENSE AGREEMENT, AMGEN MAKES NO REPRESENTATIONS OR WARRANTIES OF ANY KIND, EXPRESS OR IMPLIED, STATUTORY OR OTHERWISE, WITH RESPECT TO ANY SERVICE PROVIDED HEREUNDER OR FINISHED DRUG PRODUCT DELIVERED HEREUNDER, INCLUDING WARRANTIES OF TITLE, FITNESS FOR A PARTICULAR PURPOSE, MERCHANTABILITY, VALIDITY, AND NON-INFRINGEMENT OF INTELLECTUAL PROPERTY RIGHTS.

6. CONTRACTUAL RELATIONSHIP. Nothing contained in this Supply Agreement shall be construed as creating a partnership, joint venture, agency, trust, employer-employee relationship, or other association of any kind, each Party being individually responsible only for its obligations as set forth in this Supply Agreement.

7. CONFIDENTIALITY. Each Party agrees to protect the confidentiality of any Confidential Information received from the other Xxxxx pursuant this Supply Agreement in accordance with Article 9 of the License Agreement, which article is incorporated herein by reference.

8. INTELLECTUAL PROPERTY.

8.1 License Grant to Amgen. Subject to the terms and conditions of this Supply Agreement, Company hereby grants to Amgen a non-exclusive, non-transferable, fully-paid, and royalty-free license, with the right to sublicense to Subcontractors (prior approved by Company in writing), to use Company Proprietary Technology to perform the Services under this Supply Agreement.

8.2 No Implied Licenses. Except as expressly provided in this Article, nothing contained in this Supply Agreement is intended to confer by implication, estoppel, or otherwise, upon any Party any license or rights in any Intellectual Property Rights of the other Party.

9. LIMITATION OF LIABILITY.

9.1 The provisions of Section 8.2 of the License Agreement shall apply mutatis mutandis to this Supply Agreement.

10. MISCELLANEOUS.

10.1 General. The provisions of Sections 11.3 through 11.8 (inclusive) and 11.10 through 11.14 (inclusive) of the License Agreement are incorporated herein by reference and apply hereto mutatis mutandis.

10.2 Amendments. No amendment, supplement or other modification to any provision of this Supply Agreement shall be binding unless in writing and signed by both Parties.

10.3 Entire Agreement. This Supply Agreement, together with the License Agreement and the Quality Agreement, constitute the entire agreement between the Parties and supersedes all prior and contemporaneous agreements and understandings, both written and oral, between the Parties with respect to the subject matter hereof.

10.4 UN Convention. The United Nations Convention on Contracts for the International Sale of Goods shall have no application to, and shall be of no force and effect with respect to, this Supply Agreement or the matters herein set forth or contemplated.

[Signature page follows]

IN WITNESS WHEREOF, the authorized representatives of the Parties have executed this Supply Agreement as of the date first set forth above.

SCHEDULE

INVENTORY

Batch#

Quantity of

Vials

Expiry Date

Notes

[*]

SCHEDULE

SERVICES

1. Description of the Services. The Services to be performed at Amgen’s Facility are as follows: [*]

2. Description of the Finished Drug Product. AMG 745 material [*]

3. Delivery Dates. Amgen shall make the Finished Drug Product set forth on the Inventory Schedule available for pick-up at Amgen’s Facility warehouse on a date to be mutually agreed by the parties in writing at least three (3) weeks in advance of the pickup date, which shall be [*].

Schedule Licensed

Know-How

[*]

[32 pages omitted]

Schedule

Licensed Materials

[*]

[4 pages omitted]

Schedule

Licensed Patents

[*]

[6 pages omitted]

Schedule

Milestones and Royalties

1.	Milestone Payments: The Milestone Events and Milestone Payments to be made pursuant to Section 3.3 of the Agreement are as follows:


Milestone Event (Product)	Payment
*Development Milestones with respect to the Product*
[*]		[*]
*Commercial Milestones with respect to the Product*
[*]		[*]

2.	Royalties: The royalty rates payable under Section 3.4 of the Agreement with respect to Net Sales of Product are as follows:

(i)

[*] on the portion of annual Net Sales for the Product less than [*];

(ii)

[*] on the portion of annual Net Sales for the Product between [*] and [*], inclusive; and

(iii)

[*] on the portion of annual Net Sales for the Product greater than [*].

For the avoidance of doubt, if the Product is Covered by more than one Licensed Patent, the above royalty shall be paid only once.

Third Party Payments. In the event that Company or any of its Affiliates or Sublicensees obtains a license under Patent Rights of a Third Party in any country in the Territory that Company or its Affiliate or Sublicensee, on the advice of patent counsel, determines, in the absence of a license thereunder, would be considered to be Infringed by the development, manufacture, use, sale, offer for sale or import of the Product sold by Company (or its Affiliate or Sublicensee) in such country (in each case, a “Necessary Third Party License”), then Company may deduct [*] of the royalties actually paid to such Third Party under such Necessary Third Party License with respect to sales of the Product in such country from the royalty payments owed to Amgen pursuant to Section 2 of this Milestones and Royalties Schedule with respect to Net Sales of the Product in such country.

4.	No Valid Claim. In the event that the Product is not Covered by at least one (1) Valid Claim of a Licensed Patent within the Territory, then the royalty rates set forth in Section 2(a) of this Milestones and Royalties Schedule with respect to the Product shall be reduced by [*].

Maximum Deduction. In no event, however, shall a deduction, or deductions, in the royalty rate pursuant to Section 3 of this Milestones and Royalties Schedule and Section 4 of this Milestones and Royalties Schedule, reduce the royalty rate payable by Company on Net Sales of a the Product during a given calendar quarter pursuant to Section 2 of this Milestones and Royalties Schedule by more than [*] in the aggregate.

Mutual Convenience of the Parties. The royalty and other payment obligations set forth hereunder have been agreed to by the Parties for the purpose of reflecting and advancing their mutual convenience, including the ease of calculating and paying royalties and other amounts to Amgen. Company hereby stipulates to the fairness and reasonableness of such royalty and other payment obligations and covenants not to allege or assert, nor to allow any of its Affiliates or Sublicensees to allege or assert, nor further to cause or support any other Third Parties to allege or assert, that any such royalty or other payment obligations are unenforceable or illegal in any way.

Schedule

Permitted CMOs

[*]

Schedule

Pre-Existing Agreements

[*]

Schedule

Press Release

[Schedule begins on following page.]

Amgen to License Assets to Atara Biotherapeutics, Xxxxxxx Xxxxxxx Xxxxxxxx & Xxxxx’ (KPCB) Newly Formed Drug Development Company

September x, 2012, Thousand Oaks, CA - Amgen (NASDAQ: AMGN) and KPCB today announced an agreement that licenses six Amgen assets to Atara Biotherapeutics, a newly formed drug development company financed by KPCB. The in-licensed assets from Amgen are in various stages of development, from preclinical to early clinical. These drugs will form the foundation of Atara’s focus on developing innovative drug therapies for patients with cancer and chronic diseases, including nephrology and oncology. Financial terms of the transaction are not being disclosed.

Atara will have facilities in both the Bay Area and Thousand Oaks, Calif., where it can help broaden the biotechnology hub around Amgen. The Atara leadership team will be comprised of individuals having previous experience from both Amgen and KPCB. Amgen will have a minority equity interest in Atara, with rights to an observer seat on Atara’s Board of Directors.

“Amgen is excited to partner with KPCB, a preeminent venture capital firm, to xxxxxx a creative business model that will help advance molecules in Amgen’s pipeline to treat serious illness,” said Xxxx X. Xxxxxx, M.D., executive vice president of Research and Development at Amgen. “The creation of Atara Biotherapeutics also provides the opportunity to further xxxxxx biotechnology innovation in Amgen’s headquarters’ communities.”

“The model for Atara will enable us to build on Amgen’s research to bring a promising group of therapeutics to patients with serious illnesses, enabling them to have a better quality of life,” said Xx. Xxxxx Xxxxxxxxxxx, CEO Xxxxx Biotherapeutics (former partner at KPCB).

About Xxxxxxx Xxxxxxx

Since its founding in 1972, Xxxxxxx Xxxxxxx Xxxxxxxx & Xxxxx has backed entrepreneurs in more than 500 ventures including AOL, Xxxxxx.xxx, Citrix, Compaq, Electronic Arts, Google, Groupon, Intuit, Juniper Networks, Netscape, Sun, Symantec, Verisign, webMD and Zynga. This also includes lifesciences companies Genentech, Genomic Health, Idec and Onyx to name a few. KPCB portfolio companies employ more than 350,000 people worldwide. More than 150 of the firm’s portfolio companies have gone public, and many other KPCB ventures have achieved success through mergers and acquisitions. KPCB focuses its global investments in three practice areas - digital, greentech and life sciences - and provides entrepreneurs with company-building expertise out of its offices in Silicon Valley, Beijing and Shanghai.

About Amgen Amgen discovers, develops, manufactures and delivers innovative human therapeutics. A biotechnology pioneer since 1980, Amgen was one of the first companies to realize the new science’s promise by bringing safe, effective medicines from lab to manufacturing plant to patient. Amgen therapeutics have changed the practice of medicine, helping millions of people around the world in the fight against cancer, kidney disease, rheumatoid arthritis, bone disease and other serious illnesses. With a deep and broad pipeline of potential new medicines, Amgen remains committed to advancing science to dramatically improve people’s lives. To learn more about our pioneering science and vital medicines, visit xxxx://xxx.xxxxx.xxx/. Follow us on xxxx://xxxxxxx.xxx/xxxxx.

Schedule

Business Plan

[Schedule begins on following page.]

[*]

[60 pages omitted]

Schedule

Product

[*]

Email Address

Contact Number

Responsibility

Xxxxxx Xxxxxxxxx

Senior Manager, Alliance Management

Xxxxx Xxxx

Specialist, International Quality