THE SYMBOL “[**]” DENOTES PLACES WHERE CERTAIN IDENTIFIED INFORMATION HAS BEEN EXCLUDED FROM THE EXHIBIT BECAUSE IT IS BOTH (i) NOT MATERIAL AND (ii) WOULD LIKELY CAUSE COMPETITIVE HARM TO THE COMPANY IF PUBLICLY DISCLOSED AMENDED AND RESTATED LICENSE...

Exhibit 4.1

THE SYMBOL “[**]” DENOTES PLACES WHERE CERTAIN IDENTIFIED INFORMATION HAS BEEN EXCLUDED FROM THE EXHIBIT BECAUSE IT IS BOTH (i) NOT MATERIAL AND (ii) WOULD LIKELY CAUSE COMPETITIVE HARM TO THE COMPANY IF PUBLICLY DISCLOSED

AMENDED AND RESTATED

LICENSE AND COLLABORATION AGREEMENT

by and between

和记黄埔医药（上海）有限公司 XXXXXXXXX MEDIPHARMA LIMITED

and

ASTRAZENECA AB (PUBL)

December 7, 2020

TABLE OF CONTENTS


			Page
1.	DEFINITIONS.		2
2.	SCOPE OF COLLABORATION AND GRANT OF LICENSES.		16
	2.1.	Scope of Collaboration.	17
	2.2.	License to AstraZeneca.	17
	2.3.	License to Xxxxxxxxx.	17
	2.4.	Joint Technology.	17
	2.5.	Sublicensing.	17
	2.6.	Right of Reference.	19
	2.7.	Delivery of Xxxxxxxxx Know-How.	19
	2.8.	Delivery of AstraZeneca Know-How.	19
	2.9.	No Other Rights.	20
3.	DECISION MAKING AND DISPUTE RESOLUTION.		20
	3.1.	Joint Steering Committee.	20
	3.2.	Other Committees.	22
	3.3.	Elevation and Dispute Resolution.	22
4.	DEVELOPMENT, REGULATORY, COMMERCIALIZATION.		24
	4.1.	Development of Collaboration Product and Diagnostic Product.	24
	4.2.	Failure of Collaboration Product.	26
	4.3.	Regulatory Matters.	26
	4.4.	Manufacture.	29
	4.5.	Commercialization.	30
	4.6.	Phase IV, Early Access Programs, and Publication Strategy.	31
5.	CONSIDERATION.		32
	5.1.	Upfront Payments.	32
	5.2.	Milestones.	32
	5.3.	Royalties.	34
	5.4.	Sales Subject to Royalties.	38
	5.5.	Fully Paid-Up, Royalty Free License.	38
	5.6.	Third Party Intellectual Property.	38
	5.7.	Development Costs.	39

TABLE OF CONTENTS (CONTINUED)



			Page
	5.8.	Reports and Payments.	43
6.	COVENANTS.		47
	6.1.	Confidentiality.	47
	6.2.	Compliance with Law.	50
	6.3	Anti-Corruption Laws.	50
	6.3.	Exclusivity.	51
	6.4.	Non-Solicitation.	55
7.	REPRESENTATIONS AND WARRANTIES.		55
	7.1.	Representations and Warranties of Each Party.	55
	7.2.	Additional Representations and Warranties of Xxxxxxxxx.	56
	7.3.	Representation by Legal Counsel.	57
	7.4.	No Inconsistent Agreements.	57
	7.5.	Disclaimer.	57
8.	INTELLECTUAL PROPERTY.		57
	8.1.	Disclosure.	57
	8.2.	Ownership.	58
	8.3.	JIPC.	58
	8.4.	Filing, Prosecution and Maintenance of Patent Rights.	58
	8.5.	Trademarks.	60
	8.6.	Enforcement of Technology Rights.	60
	8.7.	Third Party Claims.	61
	8.8.	Patent Certifications.	61
	8.9.	No Implied Licenses.	62
	8.10.	Privileged Communications.	62
	8.11.	Create Act.	62
9.	GOVERNMENT APPROVALS.		62
	9.1.	AstraZeneca’s and Xxxxxxxxx’x Obligations.	62
	9.2.	Additional Approvals.	62
	9.3.	Termination.	63
10.	TERM AND TERMINATION.		63

TABLE OF CONTENTS (CONTINUED)



			Page
	10.1.	Term.	63
	10.2.	Termination for Convenience; Termination by Mutual Agreement.	63
	10.3.	Termination for Cause.	63
	10.4.	Effect of Termination.	64
	10.5.	Rights in Bankruptcy.	67
	10.6.	Survival of Certain Obligations.	67
11.	PRODUCT LIABILITY, INDEMNIFICATION AND INSURANCE.		67
	11.1.	Indemnification by Xxxxxxxxx.	67
	11.2.	Indemnification by AstraZeneca.	68
	11.3.	Procedure.	68
	11.4.	Insurance.	70
	11.5	Tax.	70
	11.6.	Liability Limitations.	70
12.	MISCELLANEOUS.		70
	12.1.	Governing Law, Jurisdiction; Dispute Resolution.	70
	12.2.	Force Majeure.	72
	12.3.	Waiver and Non-Exclusion of Remedies.	73
	12.4.	Notices.	73
	12.5.	Entire Agreement.	74
	12.6.	Amendment.	74
	12.7.	Assignment.	74
	12.8.	No Benefit to Others.	75
	12.9.	Counterparts.	75
	12.10.	Severability.	75
	12.11.	Further Assurance.	75
	12.12.	Publicity.	75
	12.13.	Relationship of the Parties.	76
	12.14.	Subcontracting.	76
	12.16.	Construction.	76

iii

AMENDED and RESTATED LICENSE AND COLLABORATION AGREEMENT

This AMENDED AND RESTATED LICENSE AND COLLABORATION AGREEMENT (the “Agreement”) is entered into on this 7th day of December, 2020 (the “Restatement Date”), by and among 和记黄埔医药 (±海) 有限公司 Xxxxxxxxx Medipharma Limited, a company organized under the laws of the People’s Republic of China, having its place of business at Xxxxxxxx 0, 000 Xxxxxx Xxxx, Xxxxxxxxxx Hi-Tech Park, Shanghai 201203, P.R. China (“Xxxxxxxxx”) and AstraZeneca AB(publ) , a company organized under the laws of Sweden, having its place of business at X-00 0 00 Xxxxxxxxxx, Xxxxxx (“AstraZeneca”). Xxxxxxxxx and AstraZeneca may each be referred to herein individually as a “Party” and collectively as the “Parties.”

RECITALS

WHEREAS, Xxxxxxxxx and AstraZeneca entered into the License and Collaboration Agreement as of the 20th of December, 2011 (the “Effective Date”), which was amended as of 1st of August, 2016, by the First Amendment (combined, the “Original Agreement”);

WHEREAS, Xxxxxxxxx owns or otherwise controls certain patents, patent applications, technology, know-how, scientific and technical information and other proprietary rights and information relating to the research, development and manufacture of the c-Met inhibitor known as HMPL-504;

WHEREAS, AstraZeneca is engaged in the research, development and commercialization of pharmaceutical products;

WHEREAS, Xxxxxxxxx and AstraZeneca desire to collaborate, on an exclusive basis, in the development and commercialization of pharmaceutical products targeting the Collaboration Target (as defined below) and to collaborate specifically on the development and commercialization of the Collaboration Compound and Collaboration Product (as defined below);

WHEREAS, subject to the terms of this Agreement, Xxxxxxxxx wishes to grant to AstraZeneca, and AstraZeneca wishes to receive from Xxxxxxxxx, an exclusive license to develop, manufacture and commercialize the Collaboration Compound and Collaboration Product in the Field (as defined below);

WHEREAS, the First Amendment provided for Xxxxxxxxx and AstraZeneca to collaborate to develop the Collaboration Product in Papillary Renal Cell Carcinoma as the Secondary Indication through the conduct initially of a Phase III Clinical Trial; and

WHEREAS, the Parties now wish to amend and restate the Original Agreement as set out in this Agreement to provide clarity around the Parties’ roles and responsibilities, in particular in relation to the development of the Collaboration Product for a renal cell carcinoma (“RCC”) indication, particular arrangements around certain life cycle indications in China, as well as the Parties’ roles and responsibilities regarding the commercialization and manufacturing of the

Licensed Compound and Licensed Product in China.

AGREEMENT

NOW THEREFORE, in consideration of the mutual promises and covenants set forth below and other good and valuable consideration, the receipt and sufficiency of which is hereby acknowledged, the Parties agree as follows:

1.DEFINITIONS.

1.1.

“Abbreviated New Drug Application” or “ANDA” means an Abbreviated New Drug Application as defined in the FD&C Act and the regulations promulgated thereunder which references an NDA.

1.2.

“Adverse Event” means any adverse medical occurrence in a patient or clinical investigation subject that is administered a pharmaceutical product, as designated in the United States of America under 21 CFR § 312.32 and any other Applicable Law.

1.3.

“Additional RCC Registrational Trial” means any Clinical Trial for the Collaboration Product in a Secondary Indication, including for the avoidance of doubt the Second RCC Phase III Clinical Trial, conducted subsequent to or in parallel with the First RCC Phase III Clinical Trial but excluding the First RCC Phase III Clinical Trial, and with the intent to secure Regulatory Approval for the Collaboration Product in such Secondary Indication without the conduct of any further Clinical Trials.

1.4.

“Affiliate(s)” means, with respect to a Person, any Person that controls, is controlled by, or is under common control with such first Person. For purposes of this definition only, “control” means (a) to possess, directly or indirectly, the power to direct the management or policies of a Person, whether through ownership of voting securities or by contract relating to voting rights or corporate governance, or (b) to own, directly or indirectly, more than fifty percent (50%) of the outstanding voting securities or other ownership interests of such Person.

1.5.

“API Manufacturing” means the Manufacture and supply of Collaboration Compound for inclusion in a Collaboration Product Developed and Commercialized in accordance with this Agreement.

1.6.

“AstraZeneca Indemnified Party” has the meaning set forth in Section 11.1.

1.7.

“AstraZeneca Know-How” means Collaboration Know-How (other than Joint Know-How) that is conceived or developed or, in the case of patentable Know- How, Invented solely by employees of AstraZeneca or its Affiliates, or Third Parties acting on behalf of AstraZeneca or its Affiliates.

1.8.

“AstraZeneca Patent Rights” means any Patent Right that AstraZeneca Controls as of the Effective Date or that come into the Control of AstraZeneca during the Term (other than Joint Patent Rights or Patent Rights which are Xxxxxxxxx Patent Rights licensed to AstraZeneca pursuant to this Agreement) to the extent such rights (a) claim a Collaboration Compound or Collaboration Products, any method of making a Collaboration Compound or Collaboration Products, any composition or formulations of a Collaboration Compound or Collaboration Products or any method of using or administering a Collaboration Compound or Collaboration Products and (b) are actually used by AstraZeneca to Manufacture, Develop or Commercialize a Collaboration Compound or Collaboration Products.

1.9.

“AstraZeneca Technology” means AstraZeneca’s interest in (i) the AstraZeneca Know-How, and (ii) the AstraZeneca Patent Rights, and all other intellectual property rights in any of the foregoing.

1.10.

“Agreement Compound” means any compound with a molecular weight less than 1000 Da, other than a Collaboration Compound, that specifically targets the Collaboration Target and lacks material activity against other pharmaceutical targets (i.e. the IC50 value of such compound or product against another pharmaceutical target is more than thirty (30) times greater than the IC50 value of such compound or product against the Collaboration Target).

1.11.

“Applicable Laws” means all applicable statutes, ordinances, regulations, rules, or orders of any kind whatsoever of any Regulatory Authority, including the FD&C Act, Prescription Drug Marketing Act, Generic Drug Enforcement Act of 1992 (21 U.S.C. § 335a et seq.), and Anti-Kickback Statute (42 U.S.C. § 1 320a-7b et seq.) and all counterparts thereto in other jurisdictions, all as amended from time to time.

1.12.

“Back-Up Compound” means any Agreement Compound Controlled by a Party, which Agreement Compound exists on the Effective Date or is discovered or invented during the Term. Back-Up Compounds in existence on the Effective Date are set forth in Schedule 1.11

1.13.

“Calendar Quarter” means each of the three (3) consecutive month periods ending on March 31, June 30, September 30, and December 31.

1.14.

“Calendar Year” means each twelve (12) month period ending December 31st.

1.15.

“China” means the People’s Republic of China, including Hong Kong and Macau.

1.16.

“China Commercialization Arrangements” means, taken together, the Product Supply Arrangements and the SOTC Arrangements.

1.17.

“China Development Activities” has the meaning set forth in Section 5.7.1(b).

1.18.

“Change of Control” means, with respect to Xxxxxxxxx, the occurrence of (a) any one of the following events: (i) a Third Party acquires, directly or indirectly, shares of Xxxxxxxxx representing fifty percent (50%) or more of the voting shares (where voting refers to being entitled to vote for the election of directors) then outstanding of Xxxxxxxxx; (ii) Xxxxxxxxx consolidates with or merges into another corporation or entity, or any corporation or entity consolidates with or merges into Xxxxxxxxx, in either event pursuant to a transaction in which more than fifty percent (50%) of the voting shares of the acquiring or resulting entity outstanding immediately after such consolidation or merger are not held by the holders of the outstanding voting shares of Xxxxxxxxx preceding such consolidation or merger; or (iii) Xxxxxxxxx conveys, transfers or leases all or substantially all of its assets to a Third Party and (b) such acquiring or merging Third Party has an Agreement Compound which is in clinical development at the time of closing of such Change of Control (a “Competing Product”), and such Competing Product is not the subject of a divestiture committed to under Section 6.4.2.

1.19.

“Clinical Trial” means a human clinical study conducted on sufficient numbers of human subjects that is designed to (a) establish that a pharmaceutical product is reasonably safe for continued testing, (b) investigate the safety and efficacy of the pharmaceutical product for its intended use, and to define warnings, precautions and adverse reactions that may be associated with the pharmaceutical product in the dosage range to be prescribed or (c) support Regulatory Approval of such pharmaceutical product or label expansion of such pharmaceutical product.

1.20.

“Collaboration Target” means [**].

1.21.

“Collaboration Compound” means Xxxxxxxxx’x proprietary compound designated by Xxxxxxxxx on the Effective Date as “HMPL-504,” as more fully described in Schedule 1.21 and as improved or modified in connection with this Agreement, [**].

1.22.

“Collaboration Know-How” means Know-How that is conceived or developed or, in the case of patentable Know-How, Invented, by or on behalf of either or both Parties’ (or their Affiliates’) employees or Third Parties acting on such Parties’ behalf, in each case in the course of such Party’s performance under or in connection with this Agreement. For avoidance of doubt, Collaboration Know-How excludes any Know-How Controlled by a Party as of the Effective Date.

1.23.

“Collaboration Patent Rights” means Patent Rights claiming Collaboration Know-How. For avoidance of doubt, Collaboration Patent Rights excludes any Patent Rights Controlled by a Party as of the Effective Date.

1.24.

“Collaboration Product” means any pharmaceutical product in finished form that contains a Collaboration Compound, either as the sole active ingredient or in combination with one or more other active ingredients, and all present and future formulations, dosages and dosage forms thereof.

1.25.

“Collaboration Technology” means Collaboration Know-How and Collaboration Patent Rights, and all other intellectual property rights in any of the foregoing.

1.26.

“Combination Collaboration Product” means a pharmaceutical product containing as its active ingredients both a Collaboration Compound and one or more other therapeutically or prophylactically active ingredients combined in a single product.

1.27.

“Commercialization” means any and all activities of using, importing, marketing, promoting, distributing, offering for sale or selling a Collaboration Product including pre-commercial launch market development activities conducted in anticipation of Regulatory Approval of a Collaboration Product, seeking pricing and reimbursement approvals for a Collaboration Product, if applicable, preparing advertising and promotional materials, sales force training, and all interactions and correspondence with a Regulatory Authority regarding Post-Approval Clinical Trials. With respect to a Marketing Authorization Holder, Commercialization includes all activities required to fulfill ongoing regulatory obligations, including Adverse Event reporting. When used as a verb, “Commercialize” means to engage in Commercialization.

1.28.

“Commercially Reasonable Efforts” means, with respect to a Party, those efforts and resources that such Party would reasonably devote to a product or compound owned by it or to which it has rights of the type it has hereunder, which is of similar market potential at a similar stage in its development or product life, taking into account the competitiveness of the global and local marketplace, the nature and extent of market exclusivity (including patent coverage and regulatory exclusivity), the pricing and launching strategy for the respective product, the proprietary position of the product, the profitability and the relative potential safety and efficacy of the product and other relevant

factors, including technical, legal, scientific, regulatory or medical factors, all as measured by the facts and circumstances at the time such efforts are due. “Commercially Reasonable” as used herein shall be interpreted in a corresponding manner.

1.29.

“Confidential Information” means, with respect to a Party, all information (and all tangible and intangible embodiments thereof), which is Controlled by such Party, is disclosed by such Party to the other Party pursuant to this Agreement, and is designated as confidential in writing by the disclosing Party whether by letter or by use of an appropriate stamp or legend, prior to or at the time any such information is disclosed by the disclosing Party to the other Party. In addition, any information which is orally, electronically or visually disclosed by a Party, or is disclosed in writing without an appropriate letter, stamp or legend, shall constitute Confidential Information if the disclosing Party, within thirty (30) days after such disclosure, delivers to the receiving Party a written document or documents describing the information disclosed and referencing the place and date of such oral, visual, electronic or written disclosure and the names of the person(s) to whom such disclosure was made; provided, however, that any technical information disclosed at a meeting of the JSC or any other committee established pursuant to this Agreement shall constitute Confidential Information unless otherwise specified.

1.30.

“Control” or “Controlled” means, with respect to any intellectual property right, information, documents or materials of a Party, that the Party or its Affiliate owns or has a license to such intellectual property right, information, documents or materials (other than pursuant to this Agreement) and has the ability to grant access, a license, or a Sublicense to such intellectual property right, information, documents or materials to the other Party as provided in this Agreement without violating an agreement with or other rights of any Third Party; it being understood and agreed that the term “Control” shall not apply to any intellectual property right for which the licensing Party shall be required to make any payments to any Third Party in connection with the licenses granted under this Agreement unless, but only if and for such time that, the other Party agrees and does promptly pay to the licensing Party all such payments arising out of the grant of the license to the other Party (as so mutually agreed between the Parties in good faith).

1.31.

“Country-Specific Termination” has the meaning set forth in Section 10.3.1.

1.32.

“Designated Manufacturer” has the meaning set forth in Section 4.4.1.

1.33.

“Development” means all activities performed by or on behalf of either Party in the performance of any Development Plan for Collaboration Compounds, Collaboration Products and Diagnostic Products in the Fields. Development shall include, without limitation, Translational Research Activities and all activities related to research, preclinical testing, test method development and stability testing, toxicology, formulation, Clinical Trials, seeking Regulatory

Approval and otherwise handling regulatory affairs, statistical analysis, report writing performed pursuant to the Development Plan with respect to Collaboration Products. Development shall not include Manufacturing or Commercialization. When used as a verb, “Develop” means to engage in Development.

1.34.

“Development Budget” means the written budget that sets forth, for the time period covered by the Development Plan, the total budget for the Parties to perform activities pursuant to the Development Plan. The initial Development Budget is attached hereto as Schedule 1.34 and may be amended from time to time by the Parties in accordance with Section 4.1.1 .

1.35.

“Development Plan” means the comprehensive plan for the Development of Collaboration Products for Regulatory Approval in the Field in the Territory, prepared and approved by the JSC (subject to Section 3.3) and as amended or updated from time to time as set forth in Section 4.1.1. The Development Plan shall include, without limitation, (a) an allocation of responsibilities for Development activities to be undertaken by each Party, consistent with the terms of this Agreement; (b) the Development Budget; (c) the indications in the Field for which the Collaboration Product is to be Developed; and (d) other critical activities to be undertaken, timelines, key decision points and relevant decision criteria.

1.36.

“Diagnostic Product” means a diagnostic tool intended for use in connection with a Collaboration Product.

1.37.

“Disclosing Party” has the meaning set forth in Section 6.1.1.

1.38.

“Effective Date” means the date of this Agreement first set forth above.

1.39.

“Excess Profits” means amounts accruing to Xxxxxxxxx in respect of China Commercialization Arrangements which exceed the amounts Xxxxxxxxx is due by virtue of Section 5.3.1.

1.40.

“Exclusivity Period” has the meaning set forth in Section 6.4.1.

1.41.

“FD&C Act” means the United States of America Federal Food, Drug, and Cosmetic Act, as amended, and the regulations promulgated thereunder.

1.42.

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

1.43.

“Field” means all diagnostic, prophylactic and therapeutic uses of a Collaboration Product, in any formulation or dosage form, for any and all indications in humans.

1.44.

“Financial Records” has the meaning set forth in Section 5.8.6.

1.45.

“First Commercial Sale” means, with respect to a Collaboration Product and any country of the Territory, the first sale of such Collaboration Product under this Agreement for use in the Field to a Third Party in such country, after such Collaboration Product has been granted Regulatory Approval by the competent Regulatory Authorities in such country.

1.46.

“First RCC Phase III Clinical Trial” shall mean the Phase III clinical trial SAVOIR, identified by AZ code D5082C00003.

1.47.

“Force Majeure” has the meaning set forth in Section 12.2.

1.48.

“GAAP” means United States of America generally accepted accounting principles, as in effect from time to time.

1.49.

“Generic Product” means, on a country-by-country basis and Collaboration Product-by-Collaboration Product basis, a drug product independently developed and commercialized by a Third Party that (a) contains the same active pharmaceutical ingredient(s) as the Collaboration Product, (b) [**] and, (c) (i) for purposes of the United States, is approved in reliance on the prior Regulatory Approval of such Collaboration Product, as determined by the FDA, or, (ii) for purposes of a country outside the United States, is approved in reliance on the prior Regulatory Approval of such Collaboration Product, as determined by the applicable Regulatory Authority.

1.50.

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

1.51.

“Xxxxxxxxx Indemnified Party” has the meaning set forth in Section 11.2.

1.52.

“Xxxxxxxxx Know-How” means (a) Know-How that is Controlled by Xxxxxxxxx as of the Effective Date or that comes into the Control of Xxxxxxxxx during the Term (other than Joint Know-How and Know-How which is AstraZeneca Know-How licensed to Xxxxxxxxx pursuant to this Agreement) to the extent necessary or useful to Manufacture, Develop or Commercialize a Collaboration Compound or Collaboration Product, including any method of making a Collaboration Compound or Collaboration Product, any composition or formulations of a Collaboration Compound or Collaboration Product or any method of using or administering a Collaboration Compound or Collaboration Product and (b) Collaboration Know-How (other than Joint Know-How) that is conceived or developed or, in the case of patentable Know-How, Invented, solely by employees of Xxxxxxxxx or its Affiliates, or Third Parties acting on behalf of Xxxxxxxxx or its Affiliates.

1.53.

“Xxxxxxxxx Patent Rights” means any Patent Right that is Controlled by Xxxxxxxxx as of the Effective Date or that comes into the Control of Xxxxxxxxx

during the Term (other than Joint Patent Rights and Patent Rights which are AstraZeneca Patent Rights licensed to Xxxxxxxxx pursuant to this Agreement) to the extent such rights claim a Collaboration Compound or Collaboration Product, any method of making a Collaboration Compound or Collaboration Product, any composition or formulations of a Collaboration Compound or Collaboration Product or any method of using or administering a Collaboration Compound or Collaboration Product. The Xxxxxxxxx Patent Rights existing as of the Effective Date are set forth on Schedule 1.49.

1.54.

“Xxxxxxxxx Supply FTE Costs” means, to the extent that pursuant to Section 4.4.3, Xxxxxxxxx is managing the Designated Manufacturer in China, 6 FTEs at $150,000 per annum during the Royalty Period.

1.55.

“Xxxxxxxxx Technology” means Xxxxxxxxx’x interest in (a) the Xxxxxxxxx Know-How and (b) the Xxxxxxxxx Patent Rights, and all other intellectual property rights in any of the foregoing.

1.56.

“IFRS” means International Financial Reporting Standards, as in effect from time to time.

1.57.

“Indemnification Claim Notice” has the meaning set forth in Section 11.3.

1.58.

“Indemnified Party” has the meaning set forth in Section 11.3.

1.59.

“Indemnifying Party” has the meaning set forth in Section 11.3.

1.60.

“Indirect Taxes” means value added taxes, sales taxes, consumption taxes and other similar taxes and the associated taxes or surcharges and stamp duty.

1.61.

“Initiation” means dosing of the first human subject of a Clinical Trial.

1.62.

“Infringement” has the meaning set forth in Section 8.6.1.

1.63.

“Invented” means the act of invention by inventors, as determined in accordance with the patent laws of the United States of America.

1.64.

“Joint Know-How” means any Collaboration Know-How that is conceived or developed or, in the case of patentable Know-How, Invented jointly by an employee of Xxxxxxxxx or its Affiliates (or a Third Party acting on any of their behalf) and an employee of AstraZeneca or its Affiliates (or a Third Party acting on any of their behalf).

1.65.

“Joint Patent Right” means any Patent Right that claims Joint Know-How and is Invented by one or more employees or agents of Xxxxxxxxx or its Affiliates (or a Third Party acting on any of their behalf) together with one or more employees or agents of AstraZeneca or its Affiliates (or a Third Party acting on any of their behalf).

1.66.

“Joint Technology” means Joint Know-How, Joint Patent Rights, and all other intellectual property rights therein.

1.67.

“JSC” has the meaning set forth in Section 3.1.

1.68.

“Know-How” means all inventions, discoveries, data, information (including scientific, technical or regulatory information), processes, methods, techniques, materials, technology, results, analyses, laboratory data, data arising from Clinical Trials and Post-Approval Clinical Trials, and other know-how, whether or not patentable, including pharmacology, toxicology, drug stability, manufacturing and formulation data, methodologies and techniques, clinical and non-clinical safety and efficacy studies, marketing studies, absorption, distribution, metabolism and excretion studies.

1.69.

“Liability” has the meaning set forth in Section 11.1.

1.70.

“Litigation Conditions” has the meaning set forth in Section 11.3.

1.71.

“Major Market Country” means each of [**].

1.72.

“Manufacture,” “Manufactured” or “Manufacturing” means all activities associated with the production, manufacture, processing, filling, finishing, packaging, labeling, shipping and storage of Collaboration Products to be Developed or Commercialized under this Agreement, including API Manufacturing, whether such activities are conducted by a Party, its Affiliates or a Third Party contractor of such Party. When used as a verb, “Manufacture” means to engage in Manufacturing.

1.73.

“Net Sales” means, on a country-by-country and Collaboration Product-by-Collaboration Product basis, with respect to any period for each country, the gross amounts (the “Gross Sales”) invoiced by a Party, its Sublicensees or its Affiliates, as applicable, to unrelated Third Parties for sales of a Collaboration Product in the Field in such country, less the following deductions to the extent included in the gross invoiced sales price for such Collaboration Product or otherwise directly paid or incurred by a Party, its Sublicensees or its Affiliates with respect to the sale of such Collaboration Product in such country: [**]

[**]. Net Sales will be determined in accordance with GAAP or IFRS, as applicable. For purposes of determining Net Sales, the Collaboration Products shall be deemed to be sold when invoiced and a “sale” shall not include, and no royalties shall be payable on, transfers by AstraZeneca, its Affiliates or Sublicencees of free samples of Collaboration Products or clinical trial materials containing a Collaboration Compound or Collaboration Product, or transfers of Collaboration Product to patients under AstraZeneca’s Patient Assistance Program in the United States or any similar programs in other countries, or other transfers or dispositions for charitable, promotional, pre-clinical, clinical, manufacturing, testing or qualification, regulatory or governmental purposes.

In the event a Collaboration Product is sold as a Combination Collaboration Product, Net Sales of the Collaboration Product will be calculated, for each applicable Calendar Quarter, as follows:

(i)

If the Combination Collaboration Product, the Single Active Collaboration Product and a product containing solely the other therapeutically or prophylactically active ingredient(s) are sold separately, Net Sales of the Single Active Collaboration Product portion of Combination Collaboration Products will be calculated by multiplying the total Net Sales of the Combination Collaboration Product by the fraction A/(A+B), where A is the average gross selling price in the applicable country of the Single Active Collaboration Product sold separately in the same formulation and dosage, and B is the sum of the average gross selling prices in the applicable country of all products containing solely such other therapeutically or prophylactically active ingredient(s) in the Combination Collaboration Product sold separately in the same formulation and dosage.

(ii)

If the Combination Collaboration Product and the Single Active Collaboration Product are sold separately, but the average gross selling price of a product containing solely the other therapeutically or prophylactically active ingredient(s) in the Combination Collaboration Product cannot be determined, Net Sales of the Combination Collaboration Product shall be equal to the Net Sales of the Combination Collaboration Product multiplied by the fraction A/C wherein A is the average gross selling price of the Single Active Collaboration Product, and C is the average gross selling price of the Combination Collaboration Product.

(iii)

If the Combination Collaboration Product and the product containing solely other therapeutically or prophylactically active ingredient(s) in the Combination Collaboration Product are sold separately, but the average gross selling price of the Single Active Collaboration Product cannot be determined, Net Sales of the Combination Collaboration Product shall be equal to the Net Sales of the Combination Collaboration Product multiplied by the following formula: one (1) minus B/C wherein B is the average gross selling price of the product containing solely the other therapeutically or prophylactically active ingredient(s) in the Combination Collaboration Product, and C is the average gross selling price of the Combination Collaboration Product.

(iv)

If the Combination Collaboration Product and the product containing solely other therapeutically or prophylactically active ingredient(s) in the Combination Collaboration Product are sold separately, but the average gross selling price of neither the Single Active Collaboration Product nor the product containing solely the other therapeutically or prophylactically active ingredient(s) in the Combination Collaboration Product can be determined, Net Sales of the Combination Collaboration Product shall be equal to Net Sales of the Combination Collaboration Product multiplied by a mutually agreed percentage that is reasonably reflective of the relative value of each active ingredient in the Combination Collaboration Product.

The average gross selling price for the Single Active Collaboration Product and such product containing solely other therapeutically or prophylactically active ingredient(s) in the Combination Collaboration Product shall be calculated for each Calendar Quarter by dividing the sales amount by the units sold of such Single Active Collaboration Product or such other product containing solely therapeutically or prophylactically active ingredient(s) in the Combination

Collaboration Product, as published by IMS or another mutually agreed independent source. In the absence of appropriate IMS or other mutually agreed upon data, in the initial Calendar Year during which a Combination Collaboration Product is sold, a forecasted average gross selling price shall be used for the Collaboration Compound, other product containing solely therapeutically or prophylactically active ingredient(s) in the Combination Collaboration Product,or Combination Collaboration Product, as applicable. Any over- or under- payment due to a difference between forecasted and actual average gross selling prices shall be paid or credited in the second royalty payment of the following Calendar Year. In the following Calendar Year the average gross selling price of the previous Calendar Year shall apply.

1.74.

“New Drug Application” or “NDA” means a New Drug Application filed with

the FDA as described in 21 CFR § 314, or any corresponding application for Regulatory Approval (not including pricing and reimbursement approval) in any country or regulatory jurisdiction other than the U.S.

1.75.

“New Third Party License” has the meaning set forth in 5.6.1.

1.76.

“NSCLC” means non-small cell lung cancer.

1.77.

“Patent Right” means any and all (a) patent applications filed under Applicable Law in any jurisdiction, including all provisional applications, substitutions, continuations, continuations-in-part, divisions, renewals, and all patents granted thereon, (b) all patents, reissues, reexaminations and extensions or restorations by existing or future extension or restoration mechanisms, including supplementary protection certificates or the equivalent thereof and (c) any other form of government-issued right substantially similar to any of the foregoing.

1.78.

“Person” means an individual, sole proprietorship, partnership, limited partnership, limited liability partnership, corporation, limited liability company, business trust, joint stock company, trust, incorporated association, joint venture, or similar entity or organization, including a government or political subdivision or department or agency of a government.

1.79.

“Pharmacovigilance Agreement” has the meaning set forth in Section 4.3.5.

1.80.

“Phase I Clinical Trial” means a Clinical Trial defined in 21 C.F.R. 3 12.21(a), as may be amended from time to time, or any equivalent thereto in any other jurisdiction.

1.81.

“Phase II Clinical Trial” means a Clinical Trial defined in 21 C.F.R. 3 12.21(b), as may be amended from time to time, or any equivalent thereto in any other jurisdiction.

1.82.

“Phase III Clinical Trial” means a Clinical Trial defined in 21 C.F.R. 3 12.21(c), as may be amended from time to time, or any equivalent thereto in any jurisdiction.

1.83.

“Phase IV Clinical Trial” means a Clinical Trial conducted after a Collaboration Product achieves Regulatory Approval, carried out for purposes of conducting safety surveillance and ongoing technical support of the Collaboration Product.

1.84.

“Post-Approval Clinical Trial” means any Clinical Trial for use of a Collaboration Product in an indication, other than a Phase III Clinical Trial or Phase IV Clinical Trial, to be conducted after a Regulatory Approval for such indication. Post-Approval Clinical Trial shall also include investigator- sponsored studies in approved indications and indications for which regulatory approval has not yet been granted. To the extent there is a pre-clinical component of a Post-Approval Clinical Trial, the pre-clinical work will be

considered part of the Post-Approval Clinical Trial.

1.85.“Primary Indication” means [**], as more particularly defined in the Development Plan.

1.86.

“Product Supply Arrangements” means the arrangements to be agreed by the Parties whereby AstraZeneca licenses manufacturing rights to Xxxxxxxxx and Xxxxxxxxx supplies Collaboration Product to the AstraZeneca China legal entity, at the Product Supply Price. Such arrangements shall be formalized under a separate manufacturing license agreement and supply agreement to be negotiated and agreed between the Parties and/or their Affiliates (in the form of one or more agreements).

1.87.

“Product Supply Price” means the price at which Xxxxxxxxx shall sell the Collaboration Product to the AstraZeneca China legal entity under the Product Supply Arrangements.

1.88.

“Receiving Party” has the meaning set forth in Section 6.1.1.

1.89.

“Recipients” has the meaning set forth in Section 6.1.1.

1.90.

“Regulatory Approval” means, with respect to a product, the approval and authorization of a Regulatory Authority in a country necessary to manufacture, distribute, sell or market such product in such country.

1.91.

“Regulatory Authority” means any national, regional, state or local regulatory agency, department, bureau, commission, council or other governmental entity in each country of the Territory involved in the granting of Regulatory Approvals.

1.92.

“Regulatory Exclusivity” means any rights or protections which are recognized, afforded or granted by any Regulatory Authority in any country or region in association with the Regulatory Approval of a Collaboration Product, providing such Collaboration Product a period of marketing exclusivity during which a Regulatory Authority that recognizes, affords or grants such marketing exclusivity shall refrain from either reviewing or approving a marketing authorization application or similar Regulatory Submission submitted by a Third Party seeking to market a generic product. Regulatory Exclusivity shall include rights conferred in the United States pursuant to the Xxxxx-Xxxxxx Amendments to the FD&C Act, the Orphan Drug Act or the Best Pharmaceuticals for Children Act or in the European Union pursuant to Section 10.1 (a)(iii) of Directive 2001 /EC/83.

1.93.“Regulatory Submissions” means applications for Regulatory Approval, notification and other submissions made to or with a Regulatory Authority that are necessary or reasonably desirable to Develop, Manufacture or Commercialize a Collaboration Product in the Field in a particular country, whether obtained before or after a Regulatory Approval in the country.

Regulatory Submissions include, without limitation, investigational new drug applications and NDAs, and amendments and supplements to any of the foregoing and their foreign counterparts, applications for pricing and reimbursement approvals, and all proposed labels, labeling, package inserts, monographs and packaging for a Collaboration Product in a particular country.

1.94.

“Regulatory Submission Party” means, with respect to a country or territory, the Party responsible for regulatory matters in such country or territory pursuant to Section 4.5.1.

1.95.

“Right of Reference” means a “Right of Reference,” as that term is defined in 21 C.F.R. § 3 14.3(b) or any analogous Applicable Law recognized outside of the United States.

1.96.

“Royalty Period” means, on a country-by-country and Collaboration Product-by-Collaboration Product basis, the period of time [**].

1.97.

“ROW Territory” means all countries of the world other than China.

1.98.

“Sales Milestone” has the meaning set forth in Section 5.2.2.

1.99.

“Second RCC Phase III Clinical Trial” means the SAMETA trial, identified by AZ code D5086C00001.

1.100.

“Secondary Indication” means [**], as more particularly defined in the Development Plan.

1.101.

“Single Active Collaboration Product” means a Collaboration Product that contains a Collaboration Compound as the sole active ingredient.

1.102.

"SOTC Arrangements” means the arrangements to be agreed by the Parties whereby AstraZeneca licenses commercialization rights to Xxxxxxxxx for provinces whereby 2-tier invoicing restrictions prohibit local supply to AstraZeneca and Xxxxxxxxx, its Sublicensees or its Affiliates, as applicable, sell, to unrelated Third Parties, Collaboration Product in the Field in such 2-tier invoicing provinces in China. Such arrangements shall be formalized under a separate commercialization license agreement, CSO agreement and SOTC agreement to be negotiated and agreed between the Parties and/or their Affiliates (in the form of one or more agreements).

1.103. “Sublicensee” means an Affiliate or Third Party that is granted a license,

sublicense, covenant not to xxx or other grant of rights under the licenses granted pursuant to Section 2 of this Agreement. “Sublicense” means an agreement or arrangement pursuant to which such a sublicense has been granted to a Sublicensee.

1.104.

“Sublicensee Material Breach” has the meaning set forth in Section 2.5.3.

1.105.

“Sublicensor” means a Party that has granted a Sublicense under rights granted to such Party under this Agreement.

1.106.

“Sued Party” has the meaning set forth in Section 8.7.2.

1.107.

“Technology” means Know-How and Patent Rights.

1.108.

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

1.109.

“Territory” means China and the ROW Territory.

1.110.

“Third Party” means any Person other than Xxxxxxxxx and its Affiliates and AstraZeneca and its Affiliates.

1.111.

“Trademark” means any trademark used by the Parties in connection with a Collaboration Product, other than the Parties’ trade names and trademarks used by the Parties to identify their companies generally.

1.112.

“Translational Research Activities” means activities relating to the Development of Diagnostic Products.

1.113.

“Valid Claim” means any claim of (a) any issued and unexpired Patent Right that claims a Collaboration Compound that has not been (i) revoked or held unenforceable, unpatentable or invalid by a Government Authority of competent jurisdiction in a decision that is not appealable or that has not been appealed within the time allowed for appeal or (ii) abandoned, disclaimed, denied or admitted to be invalid or unenforceable through reissue, re-examination or disclaimer or otherwise, or (b) any patent application that claims a Collaboration Compound that has not been (i) cancelled, withdrawn or abandoned without being refiled in another application in the applicable jurisdiction or (ii) finally rejected by an administrative agency or Government Authority of competent jurisdiction in a decision that is not appealable or that has not been appealed within the time allowed for appeal, provided that, on a country-by-country basis, a patent application pending for more than [**] from the priority date of such application shall not be considered to have any Valid Claim for purposes of this Agreement from and after such [**] date unless and until a patent with respect to such application issues.

1.114.

“Withholding Taxes” has the meaning set forth in Section 5.8.2.

2.	SCOPE OF COLLABORATION AND GRANT OF LICENSES.

2.1. Scope of Collaboration. The Parties wish to enter into this Agreement (a) to co- Develop, Manufacture and Commercialize the Collaboration Compound and Collaboration Products in the Field in the Territory and (b) to develop, manufacture and commercialize Agreement Compounds, on an exclusive basis, in accordance with Section 6.3 , in each case ((a) and (b)), in accordance with the terms and conditions of this Agreement.

2.2. License to AstraZeneca. Subject to the terms and conditions of this Agreement, Xxxxxxxxx hereby grants to AstraZeneca, effective on the Effective Date, (a) a royalty- bearing, co-exclusive license, with the right to sublicense as set forth in Section 2.5, under the Xxxxxxxxx Technology and Xxxxxxxxx’x interest in the Joint Technology, to Develop the Collaboration Compound and Collaboration Products in the Field in the Territory in accordance with the terms of this Agreement and (b) a royalty-bearing, exclusive (even as to Xxxxxxxxx subject to Section 4.4) license, with the right to sublicense as set forth in Section 2.5, under the Xxxxxxxxx Technology and Xxxxxxxxx’x interest in the Joint Technology, to Manufacture and Commercialize the Collaboration Products in the Field in the Territory.

2.3. License to Xxxxxxxxx. Subject to the terms and conditions of this Agreement, AstraZeneca hereby grants to Xxxxxxxxx a royalty-free, co-exclusive license, with the right to sublicense as set forth in Section 2.5, under the AstraZeneca Technology and AstraZeneca’s interest in the Joint Technology (a) to the extent necessary for Xxxxxxxxx to exercise its rights and perform its obligations under this Agreement and (b) to Develop the Collaboration Compound and Collaboration Products in the Field in the Territory in accordance with the terms of this Agreement.

2.4. Joint Technology. Subject to the terms and conditions of this Agreement (including Sections 2.2 and 2.3), each Party hereby grants the other Party a worldwide, irrevocable, non-exclusive, perpetual, royalty-free, fully paid up, freely sublicensable right and license to exploit the Joint Technology in any manner without compensating or accounting to the other Party.

2.5. Sublicensing.

2.5.1.AstraZeneca Right to Sublicense.

(a)AstraZeneca shall have the right to grant Sublicenses under the rights granted to AstraZeneca in Section 2.2 to its Affiliates and to Third Parties for the Development, Manufacture and Commercialization of Collaboration Compounds and Collaboration Products in the Field, provided that AstraZeneca shall (i) remain responsible for the performance of its Sublicensees under this Agreement, including for all payments due hereunder; and (b) cause its Sublicensees to comply with the terms of this Agreement.

(b)Each Sublicense (i) shall be subject and subordinate to, and consistent with, the terms and conditions of this Agreement; (ii) shall not diminish, reduce or eliminate any of AstraZeneca’s obligations under this Agreement; (iii) shall require the Sublicensee(s) to comply with all applicable terms of this Agreement (except for the payment obligations, for which AstraZeneca shall

remain financially responsible); (iv) shall require that any Sublicensee grant to AstraZeneca a Right of Reference to the same extent of the Right of Reference granted to AstraZeneca pursuant to Section 2.6.1; and (v) shall prohibit further sublicensing except on terms consistent with this Section 2.5.1. AstraZeneca shall provide Xxxxxxxxx with a complete copy of each Sublicense granted to a Third Party within thirty (30) days after execution thereof; provided, however, that AstraZeneca may redact any Confidential Information from such Sublicense to the extent that such redactions do not reasonably impair Xxxxxxxxx’x ability to ensure compliance with this Agreement.

2.5.2.Xxxxxxxxx Right to Sublicense.

(a)Xxxxxxxxx shall have the right to grant Sublicenses under the rights granted to Xxxxxxxxx in Section 2.3 to its Affiliates and to Third Parties for the Development of the Collaboration Compound and Collaboration Products in the Field in any country; provided that Xxxxxxxxx shall (i) shall remain responsible for the performance of its Sublicensees under this Agreement, including for all payments due hereunder; and (ii) cause its Sublicensees to comply with the terms of this Agreement.

(b)Each Sublicense (i) shall be subject and subordinate to, and consistent with, the terms and conditions of this Agreement; (ii) shall not diminish, reduce or eliminate any of Xxxxxxxxx’x obligations under this Agreement; (iii) shall require the Sublicensee(s) to comply with all applicable terms of this Agreement; (iv) shall require that any Sublicensee grant to Xxxxxxxxx a Right of Reference to the same extent of the Right of Reference granted to Xxxxxxxxx pursuant to Section 2.6.2; and (v) shall prohibit further sublicensing except on terms consistent with this Section 2.5.2. Xxxxxxxxx shall provide AstraZeneca with a complete copy of each Sublicense within thirty (30) days after execution thereof; provided, however, that Xxxxxxxxx may redact any Confidential Information from such Sublicense to the extent that such redactions do not reasonably impair AstraZeneca’s ability to ensure compliance with this Agreement.

2.5.3.Breach of Sublicense. In the event of an uncured material breach by any Sublicensee under a Sublicense that would constitute a material breach of the Sublicensor’s obligations under this Agreement (a “Sublicensee Material Breach”), the Sublicensor shall provide prompt written notice of such Sublicensee Material Breach to the other Party and shall use Commercially Reasonable Efforts to remedy such Sublicensee Material Breach; provided, however, that if the Sublicensor is unable to cure such Sublicensee Material Breach in accordance with Section 10.3.1 of this Agreement, such Sublicensee Material Breach shall be deemed to be an uncured material breach by the Sublicensor under this Agreement.

2.5.4.Effect of Termination on Sublicenses. In the event of a termination of this Agreement pursuant to Section 10 while a Sublicense granted under Section 2.5 is in effect, the terms of this Section 2.5.4 shall apply, provided that the Sublicensee is not in default under the applicable Sublicense and such Sublicensee certifies in writing to the non-terminating Party that (x) it is not in default under the applicable Sublicense, (y) such Sublicensee agrees to be bound by the

terms of this Agreement applicable to the Sublicensor and (y) such Sublicensee agrees to the following additional terms:

(a)All of the Sublicensee’s obligations under the Sublicense shall remain in effect as obligations to the non-terminating Party and shall be enforceable solely by such Party as a third party beneficiary. The Sublicensee’s rights under the Sublicense that do not exceed, and are not inconsistent with, the Sublicensor’s rights under this Agreement, whether in scope, duration, nature or otherwise, shall survive termination of the Sublicense.

(b)All of the Sublicensor’s rights under the Sublicense shall remain in effect, may be exercised solely by the non-terminating Party as a third party beneficiary and shall inure to the exclusive benefit of the non-terminating Party. All obligations of the Sublicensor under the Sublicense that exceed or are not consistent with the Sublicensor’ s obligations under this Agreement, whether in scope, duration, or otherwise, shall terminate.

2.6. Right of Reference.

2.6.1.AstraZeneca Right of Reference. Xxxxxxxxx hereby grants to AstraZeneca and its Sublicensees a Right of Reference to all data included in the Regulatory Submissions and Regulatory Approvals Controlled by Xxxxxxxxx and its Affiliates relating to a Collaboration Compound or Collaboration Products to the extent necessary to obtain Regulatory Approval of any Collaboration Product in the Field in any country of the ROW Territory, and Xxxxxxxxx shall provide a signed statement to this effect, if requested by AstraZeneca, in accordance with 21 C.F.R. § 314.50(g)(3) (or any analogous Applicable Law recognized outside of the United States).

2.6.2.Xxxxxxxxx Right of Reference. AstraZeneca hereby grants to Xxxxxxxxx and its Sublicensees a Right of Reference to all data included in the Regulatory Submissions and Regulatory Approvals Controlled by AstraZeneca and its Affiliates relating to Collaboration Products to the extent necessary or useful to Develop or Manufacture Collaboration Compounds or Collaboration Products in the Field in China, and AstraZeneca shall provide a signed statement to this effect, if requested by Xxxxxxxxx, in accordance with 21 C.F.R. § 3 14.50(g)(3) (or any analogous Applicable Law recognized outside of the United States).

2.7. Delivery of Xxxxxxxxx Know-How. At no cost to AstraZeneca, within [**] days after the Effective Date, Xxxxxxxxx shall transfer to AstraZeneca true and complete copies of all Xxxxxxxxx Know-How (in electronic or hard copy format) with, where applicable (and within reason), a translation into English. Thereafter during the Term, from time to time and otherwise upon AstraZeneca’s request, Xxxxxxxxx shall provide AstraZeneca with true and complete copies of updates to the Xxxxxxxxx Know-How (in electronic or hard copy format), together with all information or assistance reasonably requested by AstraZeneca with respect to understanding and using such Xxxxxxxxx Know-How.

2.8. Delivery of AstraZeneca Know-How. At no cost to Xxxxxxxxx, for so long as the Development Plan remains in effect, from time to time and otherwise upon Xxxxxxxxx’x

request, AstraZeneca shall transfer to Xxxxxxxxx true and complete copies of all AstraZeneca Know-How (in electronic or hard copy format), together with all information or assistance reasonably requested by Xxxxxxxxx with respect to understanding and using such AstraZeneca Know-How.

2.9. No Other Rights. No rights, other than those expressly set forth in this Agreement are granted to either Party hereunder, and no additional rights shall be deemed granted to either Party by implication, estoppel or otherwise, with respect to any intellectual property rights. All rights not expressly granted by either Party to the other hereunder are reserved.

3.	DECISION MAKING AND DISPUTE RESOLUTION.

3.1. Joint Steering Committee. Within thirty (30) days of the Effective Date, the Parties shall establish a joint steering committee (the “JSC”) that will be responsible for overseeing the Development and Commercialization of Collaboration Products in the Field, and will serve as a forum for (a) exchanging data, information and Development strategy regarding the Collaboration Products and (b) keeping Xxxxxxxxx apprised of all Commercialization activities with respect to the Collaboration Products.

3.1.1.Membership. The JSC will consist of three (3) senior representatives from each Party. AstraZeneca will designate the chairperson of the JSC. The chairperson will be responsible for calling meetings and setting the agenda (which shall include a list of all participants expected at a meeting) and circulating such agenda at least five (5) days prior to each meeting and distributing minutes of the meetings within thirty (30) days following such meeting, but will not otherwise have any greater power or authority than any other member of the JSC. JSC members may be replaced by the Party with authority to designate such member but shall at all times have such expertise as appropriate to the activities of the JSC from time to time, and the JSC shall invite personnel of the Parties having non-clinical safety and animal pharmacology, pharmaceutical development, clinical, biostatistical, regulatory affairs, pharmacovigilance, formulation, manufacturing, commercial, marketing and other expertise to participate in discussions of the JSC from time to time as appropriate to assist in the activities of the JSC. The JSC may appoint subcommittees as desired.

3.1.2.Responsibilities. The JSC may discharge its responsibilities through one or more subcommittees. The JSC’s responsibilities will include, without limitation, the following:

(a)overseeing implementation of the Development Plan;

(b)reviewing and evaluating progress under the Development Plan (including compliance with the Development Budget contained therein and payment arrangements) on a quarterly basis and advising the Parties as to any necessary amendments thereto;

(c)allocating and assigning Development activities in the Development Plan between the Parties, consistent with the terms of this Agreement;

(d)approving (or establishing procedures to approve) protocols for pre-clinical studies and Clinical Trials for Development of Collaboration Products;

(e)making modifications to and performing quarterly monitoring of progress of pre-clinical studies and Clinical Trials and proposing additional studies for Collaboration Products;

(f)reviewing and approving any proposed modifications to the Development Plan, including advising the Parties as to whether a Back-Up Compound should be developed in lieu of a Collaboration Compound;

(g)coordinating the Manufacture of global supplies of a Collaboration Compound and Collaboration Product for (i) Clinical Trials and (ii) Commercialization;

(h)reviewing and commenting on Regulatory Submissions relating to Collaboration Products;

(i)facilitating the exchange of all data, information, material or results relating to Development of Collaboration Products;

(j)establishing procedures regarding the collection, sharing and reporting of Adverse Event information related to Collaboration Products consistent with the Pharmacovigilance Agreement to be entered into in accordance with Section 4.3.5;

(k)facilitating the transfer of Know-How pursuant to this Agreement;

(l)developing a strategy for performing Translational Research Activities and Developing a Diagnostic Product, as necessary, under the Development Plan and overseeing implementation of any such strategy;

(m)establishing and overseeing implementation of the Commercialization Plan;

(n)performing such other activities as are contemplated under this Agreement and that the Parties mutually agree shall be the responsibility of the Joint Steering Committee.

Notwithstanding the foregoing, in no event shall the JSC or any subcommittee of the JSC have the authority to (i) reduce or expand the obligations of the Parties under this Agreement; (ii) determine that a breach has occurred under this Agreement; (iii) waive a Party’s rights or obligations under this Agreement; or (iv) make any decision that is specified elsewhere in this Agreement as being made by one or both Parties.

3.1.3.Meetings. During the period before First Commercial Sale, the JSC will meet at such frequency as shall be established by the Parties (but, unless otherwise agreed, not less

frequently than four (4) times per year). Meetings of the JSC shall alternate between the offices of the Parties, unless otherwise agreed upon by the members of the JSC, or may be held telephonically or by video conference. Meetings of the JSC shall be effective only if at least one representative of each Party is in attendance or participating in the meeting. Members of the JSC shall have the right to participate in and vote at meetings by telephone. Each Party shall be responsible for expenses incurred by its employees and its members of the JSC in attending or otherwise participating in JSC meetings. Each Party shall use reasonable efforts to cause its representatives to attend the meetings of the JSC. If a representative of a Party is unable to attend a meeting, such Party may designate an alternate to attend such meeting in place of the absent representative.

3.1.4.Minutes and Agendas. The minutes of each JSC meeting shall provide a description in reasonable detail of the discussions held at the meeting and a list of any actions, decisions or determinations approved by the JSC. Minutes of each JSC meeting shall be prepared in English, approved or disapproved, and revised as necessary, at the next meeting.

3.2. Other Committees. The JSC may establish subcommittees as the Parties mutually deem appropriate.

3.2.1.Joint Development Committee. Promptly after the Effective Date, the JSC shall establish a joint development committee (“JDC”). The JDC shall have primary responsibility for the matters set forth in Section 3.1.2(a) - 3.1.2(f) and 3.1.2(h) - 3.1.2(j), together with such other matters as are delegated to the JDC by the JSC.

3.2.2.Joint Commercial Committee Prior to Commercialization of any Collaboration Product, the JSC shall establish a joint commercial committee (“JCC”). The JCC shall have primary responsibility for the matters set forth in Section 3.1.2(m), together with such other matters as are delegated to the JCC by the JSC.

3.2.3.Joint Diagnostic Development Committee. Promptly after the Effective Date, the JSC shall establish a joint diagnostic development committee (“JDDC”). The JDDC shall have primary responsibility for the matters set forth in Section 3.1.2(l).

3.2.4.Joint Manufacturing Committee. Promptly after the Effective Date, the JSC shall establish a joint manufacturing committee (“JMC”). The JMC shall have the primary responsibility for the matters set forth in 3.1.2(g).

3.2.5.Joint Intellectual Property Committee. Promptly after the Effective Date, the JSC shall establish a Joint IP Committee (“JIPC”). The JIPC shall have primary responsibility for establishing a strategy for the prosecution, maintenance and enforcement of intellectual property rights relating to the Collaboration Product, together with such other matters as are delegated to the JIPC by the JSC. The JIPC shall have primary responsibility for the matters set forth in Section 3.1.2(k), together with such other matters as are delegated to the JIPC by the JSC.

3.3. Elevation and Dispute Resolution. [**].

3.3.1.[**].

3.3.2.[**]:

(a)[**]

(b)[**]

(c)[**]

(d)[**]

(e)[**]

3.3.3.[**]

4.	DEVELOPMENT, REGULATORY, COMMERCIALIZATION.

4.1. Development of Collaboration Product and Diagnostic Product.

4.1.1.Development Plan. The initial Development Plan for the Collaboration Product in the Field is set forth in Schedule 1.34. The JDC will direct, coordinate and manage the Development of Collaboration Products in the Field in accordance with the Development Plan. During the Term, the JDC will review the Development Plan (including the Development Budget) on an ongoing basis, but no less frequently than once per year during the period preceding First Commercial Sale and will amend as necessary, provided that the JDC will not assign any Development activities to a Party, or allocate any Development Costs to a Party beyond those set forth in the initial Development Plan attached hereto without the other Party’s prior written consent.

4.1.2.Development Activities. Each Party shall use Commercially Reasonable Efforts to implement and conduct the Development activities assigned to it under the Development Plan, in accordance with the Development Budget and the timelines set forth in the Development Plan, and to cooperate with and provide reasonable support to the other Party in such other Party’s conduct of activities under the Development Plan. Each Party will undertake its respective Development activities in accordance with GLP, GCP, GMP, as appropriate, and with all Applicable Laws. Except for the specific responsibilities allocated to Xxxxxxxxx as set forth in the Development Plan with respect to Development activities intended to support obtaining Regulatory Approval for Collaboration Products or Diagnostic Products in China (which responsibilities shall include being sponsor of registrational trials in China, including any trials required by the China Health Authority for conditional approval), AstraZeneca will be responsible for performing all Development activities, including global studies with a China component, for the purpose of obtaining Regulatory Approval for Collaboration Product and Diagnostic Products in the ROW Territory. The Parties shall share costs and expenses under this Section 4.1.2 in accordance with the allocations set forth in Section 5.7. All Clinical Trials initiated after the Effective Date and performed by a Third Party will be conducted by agents both Parties agree have sufficient capability to ensure all Clinical Trials performed by such Third Party are conducted and reported, and can be audited to show they have been conducted and reported, to comply with standards of GCP acceptable to Regulatory Authorities globally.

4.1.3.Reports of Development Activities. Each Party shall report on Development activities undertaken by such Party in accordance with Development Plan by providing a reasonably detailed summary of all results, data and material inventions, if any, obtained from such activities, together with a summary of the Development activities that such

Party intends to undertake during the next twelve (12) months with respect to Development of a Collaboration Compound and Collaboration Product. Such reports shall be provided in English by each Party to the other at least [**] days prior to each meeting of the JDC, [**]. In addition, each Party shall, at its own expense, make appropriate scientific and regulatory personnel available to the other Party, either by telephone or in person as the Parties may mutually agree, as reasonably required to keep the other Party informed of Development activities.

4.1.4.Development Diligence Obligations. AstraZeneca shall use Commercially Reasonable Efforts to apply for and obtain Regulatory Approval of the Collaboration Product in the ROW Territory, and Xxxxxxxxx shall use Commercially Reasonable Efforts to apply for and obtain Regulatory Approval of the Collaboration Product in China, in each case, as soon as reasonably practicable. AstraZeneca shall use Commercially Reasonable Efforts to Develop or procure the Development of any Diagnostic Products reasonably necessary to Commercialize the Collaboration Products and to apply for and obtain Regulatory Approval of such Diagnostic Products in the Territory as soon as reasonably practicable.

[**]

4.2. Failure of Collaboration Product. In the event [**], such Party shall have the right to request a meeting of the JSC, which shall discuss in good faith the Back-Up Compounds then available. In such case, the following provisions shall apply.

4.2.1.Nomination of New Collaboration Compound. In the event [**], the JSC (advised by the JDC, as appropriate) shall promptly nominate a Back-Up Compound to replace the Collaboration Compounds (such Back-Up Compound, a “New Collaboration Compound”), and the Parties shall promptly meet to negotiate in good faith a definitive agreement (or amendment to this Agreement, if appropriate) that sets forth each Party’s rights and obligations with respect to such New Collaboration Compound. Until execution of any such definitive agreement (or amendment), the terms and conditions of this Agreement applicable to the Collaboration Compound shall continue in full force and effect.

4.2.2.Failure to Agree on New Collaboration Compound. In the event the Parties do not mutually agree as to whether the Parties should continue activities under the Development Plan with respect to the Collaboration Compound, either Party shall have the right to terminate this Agreement under Section 10.2, and the effects of termination set forth in Section 10.4.1 shall apply.

4.3. Regulatory Matters.

4.3.1.Responsibility for Regulatory Interactions.

(a)Subject to the terms and conditions of this Agreement, including Section 4.3.1(d) AstraZeneca shall be responsible for all regulatory matters relating to Collaboration Products and Diagnostic Products in all countries and territories

other than China, and Xxxxxxxxx shall be responsible for all regulatory matters relating to Collaboration Products and Diagnostic Products in China. Xxxxxxxxx shall be the Regulatory Submission Party for China, and AstraZeneca shall be the Regulatory Submission Party for the ROW Territory. The costs and expenses associated with the Parties’ activities under this Section 4.3.1 shall be allocated as set forth in Section 5.7. With regard to the Development of a Diagnostic Product, it is the Parties’ current intention that such Development will be undertaken by a Third Party under contract to the Parties and such Third Party will be responsible for the regulatory matters relating to the Diagnostic Products.

(b)Without limiting the foregoing, subject to the terms and conditions of this Agreement, including Section 4.3.1(d), the Regulatory Submission Party shall have sole authority in the applicable country or territory with respect to (i) obtaining Regulatory Approvals for Collaboration Products and subsequently maintaining such Regulatory Approvals, (ii) communicating with Regulatory Authorities about Collaboration Products and (iii) preparing and submitting supplements, communications, annual reports, Adverse Event reports, manufacturing changes, supplier designations and other related regulatory filings and Regulatory Submissions (including with respect to Phase IV Clinical Trials and Post-Approval Clinical Trials, in each case as approved in accordance with Section 4.5.1). Xxxxxxxxx shall give AstraZeneca a reasonable opportunity and reasonable time to review and comment on regulatory submissions in China pertaining to safety, Phase IV Clinical Trials, and Post-Approval Clinical Trials before such submissions are submitted to the China Health Authority, and shall reflect any reasonable comments offered by AstraZeneca.

(c)Notwithstanding anything to the contrary in this Agreement, in the event the Parties pursue Development and/or Commercialization of (i) a Collaboration Product in combination with an AstraZeneca-proprietary product, or (ii) a Combination Collaboration Product that contains an AstraZeneca-proprietary product as an active ingredient (collectively, an “AZ Proprietary Combination Product”), AstraZeneca shall be responsible for all regulatory matters relating to such AZ Proprietary Combination Product in the Territory and shall be the Regulatory Submission Party for the AZ Proprietary Combination Product in the Territory.

(d)Each Party shall keep the JSC reasonably informed regarding the status and progress of its activities conducted pursuant to this Section 4.3.1, including providing the JSC with advance notice of all meetings scheduled with a Regulatory Authority (including notice promptly after a request for a meeting received from a Regulatory Authority) involving a Regulatory Submission, providing the JSC with a copy of all substantive written correspondence from a Regulatory Authority involving a Regulatory Submission, notifying the JSC of all oral substantive correspondence from a Regulatory Authority involving a Regulatory Submission, and promptly providing the JSC with each Regulatory Submission submitted to a Regulatory Authority.

4.3.2.Regulatory Cooperation. At no cost to the other Party, other than reimbursement of a Party’s reasonable out-of-pocket costs and expenses, the Regulatory Submission Party shall provide the other Party with reasonable access to and copies of any documents, correspondence or other materials Controlled by the Regulatory Submission Party that are useful for Regulatory Submissions for Collaboration Products to be made by the other Party pursuant to Section 4.3.1, and will otherwise cooperate with the other Party with respect to such Party’s efforts to obtain and maintain Regulatory Approvals for Collaboration Products in the Field pursuant to Section 4.3.1. The parties shall also use good faith efforts to align on the indications pursued for regulatory approval in China and the ROW Territory.

4.3.3.Regulatory Meetings. The Regulatory Submission Party shall provide the other Party with notice of all meetings, conferences and discussions (including without limitation, advisory committee meetings or any other meeting of experts convened by any Regulatory Authority concerning any topic relevant to the Collaboration Product) promptly after the scheduling of such meeting, conference or discussion. The Party that does not, at the time of such meeting, own the Regulatory Submission for the Collaboration Product that is the subject of such meeting shall be entitled to have one (1) or more representatives, as appropriate under the circumstance and at its sole cost, present at all such meetings. Xxxxxxxxx and AstraZeneca, through the JDC, shall use all reasonable efforts to agree in advance on the scheduling of such meetings, conferences and discussions and on the objectives to be accomplished at such meetings, conferences and discussions and the agenda for the meetings, conferences and discussions with the Regulatory Authority. Each Party shall provide to the other Party, as soon as reasonably practicable but in no event more than two (2) Business Days after its receipt, copies of any material documents or other material correspondence received from a Regulatory Authority in China, United States, European Union or Japan pertaining to the Collaboration Compound or Collaboration Product.

4.3.4.Regulatory Audits. If a Regulatory Authority desires to conduct an inspection or audit of a Party’s facility, or a facility under contract with a Party, with regard to a Collaboration Product, then such Party shall promptly notify the other Party and permit and cooperate with such inspection and audit. Following receipt of the inspection or audit observations of such Regulatory Authority (a copy of which the audited Party will immediately provide to the other Party), the audited Party shall prepare the response to any such observations and shall provide a copy of such response to the other Party.

4.3.5.Adverse Events. Within ninety (90) days after the Effective Date, the Parties will enter into a pharmacovigilance agreement, which upon such execution will be attached as an exhibit hereto and hereby incorporated into this Agreement by reference (the “Pharmacovigilance Agreement”). The Parties shall comply with the provisions of such agreement. AstraZeneca shall maintain and will be the recognized holder of a global safety database for Adverse Event reports related to the Collaboration Product, subject to Section 4.3.1. Unless otherwise agreed to by the Parties, and subject to Section 4.3.1, the Marketing Authorization Holder (“MAH”) will respond to all safety inquiries regarding the Collaboration Product in the country or countries in which the MAH is held.

4.3.6.HGR Compliance. In performing its obligations under this Agreement, unless otherwise agreed by the Parties, Xxxxxxxxx shall apply for and obtain, and shall cause its

Affiliates or Sublicensees to apply for and obtain, all necessary filings, approvals and permits (including all human genetic resources (“HGR”) applications and corresponding HGR filing and approvals (including the main approvals, and if any, the export approvals)) that are required by the Applicable Laws, and shall consult with AstraZeneca in good faith on the strategy for such applications and filings.

4.4. Manufacture.

4.4.1.Selection of a Manufacturer for Clinical Supply. Promptly after the Effective Date, the JSC shall select one (1) or more manufacturers to Manufacture and supply Collaboration Compound and Collaboration Product for all Development activities under the Development Plan in the Territory (the “Designated Manufacturer”). In the event that the JSC cannot unanimously agree on the selection of a single Designated Manufacturer for the Territory, AstraZeneca shall have the right to select a Designated Manufacturer to Manufacture the Collaboration Compound or Collaboration Product for use in the Territory, recognizing the needs for selecting a Designated Manufacturer to Manufacture in China for the China Development Activities in order to support the rapid Regulatory Approval of the Collaboration Product in China.

4.4.2.Designated Manufacturer Agreements for Clinical Supply. Subject to oversight by the JSC, the Parties shall be jointly responsible for procuring sufficient quantities of Collaboration Compound and Collaboration Product as are necessary for the Parties to perform their respective obligations under the Development Plan. Unless the Parties agree to a single Designated Manufacturer under Section 4.4.1, Xxxxxxxxx shall (x) negotiate in good faith and enter into an agreement with a Designated Manufacturer for the Manufacture and supply of such quantities of Collaboration Compound and Collaboration Product as are necessary for Xxxxxxxxx to perform its obligations under the Development Plan (i.e., with respect to China) or (y) with AstraZeneca’s prior approval (not to be unreasonably withheld, delayed or conditioned), Manufacture and supply such quantities of Collaboration Compound and Collaboration Product itself or through an Affiliate. In the case where such agreement refers to the future commercial terms of supply of a Collaboration Compound or Collaboration Product then the prior approval of AstraZeneca to such terms shall be sought. Unless the Parties agree to a single Designated Manufacturer under Section 4.4.1, AstraZeneca shall negotiate in good faith and enter into an agreement with a Designated Manufacturer for the Manufacture and supply of such quantities of Collaboration Compound and Collaboration Product as are necessary for AstraZeneca to perform its obligations under the Development Plan (i.e., with respect to the ROW Territory). Each Party shall promptly provide to the other Party a copy of its agreement with the Designated Manufacturer promptly after execution thereof. [**]. The Parties shall share costs and expenses of procuring supply from a Designated Manufacturer under this Section 4.4.2 in accordance with the allocations set forth in Section 5.7.

4.4.3.Commercial Supply of Collaboration Compound and Collaboration Product.

(a)AstraZeneca shall be solely responsible, at its sole expense, for Manufacturing or having Manufactured commercial quantities of Collaboration Compound and Collaboration Product for sale throughout the Territory. Notwithstanding the foregoing, and to the extent that Xxxxxxxxx is the Marketing Authorisation Holder (MAH) for the Collaboration Product in China, the Parties may agree in writing on a case-by-case basis that Xxxxxxxxx may itself Manufacture the Collaboration Compound or Collaboration Product in China or engage, either directly or through an Affiliate, a Designated Manufacturer to Manufacture the Collaboration Compound or Collaboration Product in China. AstraZeneca shall have the right to consent to such arrangement, including any Designated Manufacturer and the terms on which such Designated Manufacturer is engaged by Xxxxxxxxx, such consent not to be unreasonably withheld, conditioned or delayed, and shall then provide a manufacturing license right in China to Xxxxxxxxx and the Designated Manufacturer. Xxxxxxxxx shall provide to AstraZeneca a copy of the agreement which Xxxxxxxxx has entered into with the Designated Manufacturer promptly after execution thereof and shall not (i) terminate or amend the terms of its agreement with the Designated Manufacturer without first providing notice of such termination or amendment to AstraZeneca or (ii) enter into any other agreement for the supply or Manufacture of Collaboration Compound or Collaboration Product without the prior written consent of AstraZeneca, such consent not to be unreasonably withheld, conditioned or delayed. Notwithstanding anything to the contrary set forth in this Agreement, AstraZeneca consents to Shanghai STA Pharmaceutical Product Co., Ltd. (上海合全医药有限公司) as a Designated Manufacturer engaged by Xxxxxxxxx under this Agreement.

(b)To the extent that Xxxxxxxxx maintains the MAH for the Collaboration Product in China and engages a Designated Manufacturer to Manufacture the Collaboration Compound or Collaboration Product in China, Xxxxxxxxx shall, as between the Parties, (i) be responsible for pursuing and maintaining all necessary manufacturing approvals in China, and (ii) assume all legal responsibility for the manufacture of the Collaboration Product in China and for management and oversight of the Designated Manufacturer in China. Xxxxxxxxx shall further exercise commercially reasonable efforts to negotiate a reasonable purchase price for the supply of the Collaboration Product from its Designated Manufacturer (“Designated Manufacturer Supply Price”).

(c)Prior to commercial launch of a Collaboration Product in the Field in China, AstraZeneca and Xxxxxxxxx shall negotiate in good faith a definitive Commercial Supply and Quality Assurance Agreement to memorialize and regulate manufacture and supply of the Collaboration Product in China pursuant to this Section 4.4.3.

4.5. Commercialization.

4.5.1.Commercialization Activities. As of the Effective Date, the Parties contemplate that (i) AstraZeneca shall be responsible for the Commercialization — including for

the avoidance of doubt, Phase IV Clinical Trials and Post-Approval Clinical Trials—of the Collaboration Product in the Territory and (ii) the Parties may negotiate in good faith to co- Commercialize (but not co-promote) the Collaboration Product in China. Any such co- Commercialization shall be subject to a separate written agreement of the Parties. To the extent that Xxxxxxxxx is the MAH in China, Xxxxxxxxx shall conduct all regulatory and clinical activities that are reasonably required to be conducted by the MAH or in the MAH’s name and that are necessary for the Commercialization of the Collaboration Product in the Territory (including pursuing and maintaining all necessary post-marketing approvals in China). Xxxxxxxxx shall also cooperate in good faith with AstraZeneca with regard to the conduct of Phase IV Clinical Trials and Post-Approval Clinical Trials, including by facilitating the fulfillment of AstraZeneca’s reasonable requests for clinical supply from a Designated Manufacturer of the Collaboration Compound or Collaboration Product in China pursuant to Section 4.4.3.

4.5.2.Reports of Commercialization Activities. AstraZeneca shall provide Xxxxxxxxx with quarterly reports of the activities it has undertaken with regard to Commercializing Collaboration Products in the Field in all countries and territories, including AstraZeneca’s efforts to achieve the diligence obligations set forth in Section 4.6.4. In addition, AstraZeneca shall meet with Xxxxxxxxx, at Xxxxxxxxx’x request, no more than two (2) times per year to report on the activities it has undertaken with regard to Commercializing Collaboration Products in the Field and to provide a forum for Xxxxxxxxx to provide feedback regarding such Commercialization activities, which feedback shall be reasonably considered by AstraZeneca in developing its future Commercialization strategy for a Collaboration Compound and Collaboration Products.

4.5.3.Commercialization Diligence Obligations. AstraZeneca shall use Commercially Reasonable Efforts to Commercialize Collaboration Products in the Field in the Territory. AstraZeneca shall use Commercially Reasonable Efforts to identify and procure the Commercialization of any Diagnostic Product reasonably necessary to Commercialize the Collaboration Products in the Territory. Upon the grant of a Regulatory Approval for a Collaboration Product in a country, AstraZeneca shall use Commercially Reasonable Efforts to market Collaboration Products in such country. AstraZeneca shall not, and shall ensure that its Affiliates and Sublicensees do not, seek Regulatory Approval for or Commercialize a Combination Collaboration Product in any country or territory prior to obtaining Regulatory Approval for and Commercializing in such country a Collaboration Product that is not a Combination Collaboration Product.

4.6. Phase IV, Early Access Programs, and Publication Strategy.

4.6.1.Conduct of Phase IV Clinical Trials. Neither Party shall undertake, or permit its Affiliates or Sublicensees to undertake, any pre-clinical study or Clinical Trial of any Collaboration Product, including Phase IV Clinical Trials, but excluding any studies required for Regulatory Approval or otherwise imposed by a Regulatory Authority and authorized under the Development Plan, without approval of such studies by the JSC.

4.6.2.Publication Strategy. The Parties shall coordinate worldwide publication strategy involving Collaboration Products and activities involving Collaboration Products related to scientific conferences through the JSC. Review and approval of individual manuscripts shall be delegated to appropriate working groups of the Parties. Each Party shall be afforded the

opportunity to review and approve any scientific paper or presentation with respect to any Collaboration Product proposed for publication, presentation or distribution by the other Party or its Affiliates or Sublicensees and shall have no more than [**] to complete such review and approval (or such shorter period as may reasonably be required by applicable publication deadlines promptly communicated to such Party). The Party proposing a publication or presentation shall (a) not unreasonably reject comments furnished by the other Party, (b) comply with the other Party’s request to delete references to its Confidential Information in any such publication or presentation and (c) delay publication for such reasonable period requested by the other Party to permit the filing of patent applications concerning any AstraZeneca Technology, Xxxxxxxxx Technology or Joint Technology disclosed in material proposed for such publication or presentation. In no event will Confidential Information of a Party be published without the consent of such Party.

4.6.3.Permitted Publications. Notwithstanding anything to the contrary in this Agreement, both Parties and their respective Affiliates shall be entitled to publicly disclose significant Collaboration Product achievements of the type and by the means customary for similarly situated companies, including commencement of Clinical Trials, significant factual information with respect to Clinical Trials (including numbers of patients, centers, investigators, descriptions of protocols, completion of enrollment and of treatment under Clinical Trials, safety and efficacy data and other results of Clinical Trials) and filings with and actions by Regulatory Authorities. Prior to publicly disclosing any such Collaboration Product achievement, including any results of Clinical Trials, the disclosing Party will provide the other Party with a copy of such disclosure no later than [**] business days in advance, or if such advance notice is not practicable under the circumstances, as much advance notice as the disclosing Party can reasonably provide (if any) and shall take into account the good faith and reasonable comments made by the other Party within such period.

5.CONSIDERATION.

5.1. Upfront Payments. In consideration of the rights granted to AstraZeneca under this Agreement and the investment incurred for HMPL-504 by Xxxxxxxxx prior to the date of this Agreement, AstraZeneca shall, upon receipt of an invoice, make a payment of [**] on the Effective Date as an upfront, non-creditable, non-refundable fee to Xxxxxxxxx, and such fee will not be reduced by the amount of any Indirect Taxes or Withholding Taxes required to be paid by AstraZeneca under any Applicable Law, subject, however, to Section 5.8.2 and 5.8.3. The Parties agree that AstraZeneca has provided the Upfront Payment as of the Restatement Date.

5.2. Milestones.

5.2.1.Development Milestones. As additional consideration for the rights granted to AstraZeneca under this Agreement, except as otherwise set forth below, AstraZeneca will pay Xxxxxxxxx, upon receipt of an invoice, the following non-creditable, non-refundable (except as set forth in Section 9.3) amounts, within [**] after the first occurrence of each of the following events (each, a “Development Milestone”). For the avoidance of doubt, each Development Milestone shall be paid only once during the Term, regardless of the number of Collaboration Compounds or Collaboration Products that achieve the corresponding Milestone Event:


EVENT	MILESTONE. PAYMENT
Initiation of the first Phase I Clinical Trial in China	$5,000,000 The parties agree that AstraZeneca has made this payment as of the Restatement Date.
[**]	[*] The parties agree that AstraZeneca has made this payment as of the Restatement Date.*
Initiation of the first Phase IIb Clinical Trial in the Secondary Indication (or an indication having equal or greater market potential as Secondary Indication)	$5.000.000 The parties agree that AstraZeneca has made this payment as of the Restatement Date.
[**] For the avoidance of doubt, initiation of any of the Clinical Trials set forth in Schedule 4.1.6 shall not trigger this Development Milestone.	[**]
[**]	[*] The parties agree that AstraZeneca has made this payment as of the Restatement Date.*
[**]	[**]
[**]	[**]
[**]	[**]

In determining whether, for the purposes of this Section 5.2.1, an indication has equal or greater market potential as the Primary Indication or the Secondary Indication as the case may be, the JSC shall meet to discuss in good faith whether such indication does, in fact, have

equal or greater market potential. [**].

Any Development Milestone payable under this Section 5.2.1 will not be reduced by the amount of any Indirect Taxes or Withholding Taxes required to be paid by AstraZeneca under any Applicable Law, subject, however. to Section 5.8.2 and 5.8.3.

5.2.2.Sales Milestones. As further consideration for the rights granted to AstraZeneca under this Agreement, AstraZeneca will pay Xxxxxxxxx upon receipt of an invoice the following non-creditable, non-refundable amounts within [**] days after the first occurrence of the following events (each, a “Sales Milestone”):


EVENT	MILESTONE PAYMENT
[**]	[**]
[**]	[**]
[**]	[**]

5.2.3.Notice of Milestone Event. AstraZeneca shall notify Xxxxxxxxx as promptly as reasonably practicable after the occurrence of each Development Milestone and each Sales Milestone, but in no event later than ten (10) days after the occurrence thereof.

5.3. Royalties. In addition to the payments under Sections 5.1 and 5.2, in consideration for the rights granted to AstraZeneca under this Agreement, AstraZeneca shall pay to Xxxxxxxxx the royalty payments set forth in this Section 5.3, as such may be adjusted pursuant to the terms hereof.

5.3.1.China Royalty. During the Royalty Period. subject to Section 5.3.3, Xxxxxxxxx, on a Collaboration Product-by- Collaboration Product basis, shall be entitled to receive

from AstraZeneca or its Affiliates an amount equal to [**] of annual aggregate Net Sales of each such Collaboration Product in the Field in China in such Calendar Year (or portion thereof) plus the Designated Manufacturer Supply Price and Xxxxxxxxx Supply FTE Costs with such amounts to be achieved through a combination of the amounts received by Xxxxxxxxx under the Product Supply Arrangements and SOTC Arrangements and by the payment of royalties. Within 60 days of the Restatement Date, the Parties shall negotiate in good faith the appropriate agreements to operationalize the principles set forth in this Section 5.3, such agreements to include the Product Supply Arrangements and SOTC Arrangements. The collective impact of any such agreements shall solely alter the mechanics of settlement between the parties and not alter the underlying economics, such that Xxxxxxxxx shall receive a final amount annually equivalent to the agreed contractual royalty of an amount equal to [**] of annual aggregate Net Sales of each such Collaboration Product in the Field in China in such Calendar Year (or portion thereof).

0.0.0.Xxxx of World Royalty.

(a)During the applicable Royalty Period, AstraZeneca shall pay to Xxxxxxxxx, on a country-by-country and Collaboration Product-by- Collaboration Product basis, royalties at a rate equal to the rates outlined below (“Base ROW Royalty”):

(i)[**] of Net Sales in each Calendar Year (or portion thereof) for the portion of annual aggregate Net Sales of such Collaboration Product in the Field in the ROW Territory below or equal to [**]; plus

(ii)[**] of Net Sales in each Calendar Year (or portion thereof) for the portion of annual aggregate Net Sales of such Collaboration Product in the Field in the ROW Territory greater than [**] and less than or equal to [**]; plus

(iii)[**] of Net Sales in each Calendar Year (or portion thereof) for the portion of annual aggregate Net Sales of such Collaboration Product in the Field in the ROW Territory greater than [**].

The above annual royalty rates and tiers shall start anew at the respective tiers at the start of every Calendar Year during the applicable Royalty Period.

(b)Subject to Section 5.3.2(c) below, if Regulatory Approval in a Major Market for commercialization of the Collaboration Product in a Secondary Indication is achieved, then during the applicable Royalty Period, on a country-by-country and Collaboration Product-by- Collaboration Product basis, in addition to the Base ROW Royalty, AstraZeneca shall pay Additional ROW Royalties to Xxxxxxxxx at the Additional ROW Royalty Rate set forth in accordance with the equation below, for Net Sales in each Calendar Year (or portion thereof) of such Collaboration Product in the Field in the ROW Territory:

Additional ROW Royalty Rate = Base Additional ROW Royalty Rate * [**]

Where:

● Base Additional ROW Royalty Rate is [**] until AstraZeneca has paid Additional ROW Royalties totaling [**] times the total amount that Xxxxxxxxx has invested in the Development of the Collaboration Product for the Secondary Indication (“Additional ROW Royalties First Cut off Date”). The total amount that Xxxxxxxxx has invested in the Secondary Indication shall be calculated as Xxxxxxxxx'x absolute contribution (including internal expenses and out-of-pocket costs) to (1) the First RCC Phase III Costs and (2) the costs of the Additional RCC Registrational Trials, subject to audit and reconciliation by AstraZeneca pursuant to Sections 5.8.7 through 5.8.9 mutatis mutandis. After reaching the Additional ROW Royalties First Cut Off Date, the Base Additional ROW Royalty Rate will descend to [**] of Net Sales until 24 months past the Additional ROW Royalties First Cut off Date (the “Additional ROW Royalties Second Cut off date”). After this, the Base Additional ROW Royalty Rate will be [**] of Net Sales.

● For clarity, the above formula includes the Xxxxxxxxx contribution of approximately [**] towards the First RCC Phase III Costs (which will be calculated exactly upon full completion of the First RCC' Phase III study) and the [**] Xxxxxxxxx initial contribution towards the costs of the Additional RCC Registrational Trials.

● x is Xxxxxxxxx'x absolute contribution (including internal expenses and out-of-pocket costs) to the costs of the Additional RCC Registrational Trials, minus [**], subject to audit and reconciliation by AstraZeneca pursuant to Sections 5.8.7 through 5.8.9 mutatis mutandis.

● y is the total of AstraZeneca's and Xxxxxxxxx'x absolute contributions to the costs of the Additional RCC Registrational Trials (including costs for the Second RCC Phase III Clinical Trial) minus [**] subject to audit and reconciliation by each party pursuant to Sections 5.8.7 through 5.8.9 mutatis mutandis.

By way of example.:

If the parties conducted a Second RCC Phase III Trial that cost [**] then pursuant to Section 5.7, Xxxxxxxxx would fund the [**] in costs. The [**] would be split [**] between Xxxxxxxxx and AstraZeneca, with each party

paying [**]. Accordingly, if the parties received Regulatory Approval in a Major Market for commercialization of the Collaboration Product in the RCC indication, the Additional ROW Royalty Rate initially would be calculated as follows:

[**]

(c)In the event the Additional RCC Registrational Trials do not meet their key endpoints, there is not Regulatory Approval of the Collaboration Product for commercialization in a Major Market, or if Development of all Collaboration Products for the Secondary Indication is permanently abandoned or stopped in accordance with this Agreement prior to Commercialization of any Collaboration Product for the Secondary Indication, no Additional ROW Royalties shall be payable. Notwithstanding the foregoing, the Parties will negotiate in good faith the value of any data generated through Xxxxxxxxx having funded the First RCC Phase III Clinical Trial and/or the Additional RCC Registrational Trials which is then subsequently used by AstraZeneca or its Sublicensees for Development of the Collaboration Product in any other indication (other than the Secondary Indication) and to what extent this would justify paying Xxxxxxxxx reduced Additional ROW Royalties; provided that AstraZeneca shall initiate such negotiations prior to the use of such data.

(d)The Parties acknowledge that as of the Restatement Date, (i) the First RCC Phase III Clinical Trial has been terminated; (ii) Xxxxxxxxx had contributed approximately [**] towards the First RCC Phase III Costs; (iii) Xxxxxxxxx has at its sole discretion elected to provide part of the funding required to conduct Additional RCC Registrational Trials by [**] towards the costs of the Additional RCC Registrational Trials as well as [**] of any remaining costs of the Additional RCC Registrational Trials pursuant to Section 5.7.2.; and (iv) as a result of (i) , (ii) and (iii), Xxxxxxxxx is deemed to have paid all the First RCC Phase III Costs.

(e)To the extent that Xxxxxxxxx earns Excess Profits under the China Commercialization Arrangements, any ROW Royalty due to Xxxxxxxxx under this Section 5.3.2 shall be settled firstly by way of netting off such Excess Profits with any balance remaining to be settled by way of a payment from AstraZeneca to Xxxxxxxxx. Such netting off shall solely alter the mechanics of settlement between the parties and not alter the underlying economics, such that Xxxxxxxxx shall receive a final amount annually equivalent to the agreed contractual royalty as calculated pursuant to this Section 5.3.2.

5.3.3.Adjustments in Royalty Rates. On a country-by-country basis [**], AstraZeneca shall owe royalties under Section 5.3 (as applicable to such country) on the

amount of the Net Sales of such Collaboration Product in such country at rates that are [**] of the rates otherwise payable under such Section 5.3 for the remainder of the Royalty Period.

5.4. Sales Subject to Royalties. Sales of Collaboration Product between AstraZeneca, its Affiliates and Sublicencees that are purchased for re-sale shall not be subject to royalties hereunder. Royalties shall be calculated on AstraZeneca’s and its Affiliates’ sale of the Collaboration Products to Third Parties (including distributors). Royalties shall be payable only once per unit of Collaboration Product.

5.5. Fully Paid-Up, Royalty Free License. Following the expiration of the Royalty Period for any Collaboration Product in a given country of the Territory, no further royalties shall be payable in respect of Net Sales of such Collaboration Product in such country and, thereafter, the license granted to AstraZeneca under Section 2.2 with respect to such Collaboration Product in such country shall automatically become a fully paid-up, perpetual, irrevocable, non-terminable, royalty-free, non-exclusive license.

5.6. Third Party Intellectual Property. Neither Party shall negotiate or enter into any New Third Party License without first discussing such new Third Party License at the Joint Steering Committee and complying with the provisions of this Section 5.6.

5.6.1.Terms of New Third Party Licenses. If, during the Term and after consultation with Xxxxxxxxx, AstraZeneca enters into an agreement with a Third Party in order to obtain a royalty bearing license under any Patent Right of a Third Party that, in AstraZeneca’s reasonable judgment, would be necessary for the Development, Manufacture or Commercialization of the Collaboration Compound or Collaboration Product in the Field in the Territory (a “New Third Party License”), then AstraZeneca shall be entitled, on a Collaboration Product-by-Collaboration Product and country-by-country basis, to credit against any royalty payable to Xxxxxxxxx under Section 5.3.1 or 5.3.2 [**] of any royalty (but no other payments) (the “Xxxxxxxxx Portion”) actually paid by or on behalf of AstraZeneca to such Third Party as a result of such sale; provided, however, that in no event shall any royalty payable to Xxxxxxxxx be reduced as a result of this Section 5.6.1 by more than [**] of the amount otherwise due to Xxxxxxxxx with respect to such sale. In addition, any such Xxxxxxxxx Portion shall not reduce the amounts due to Xxxxxxxxx under Section 5.3 in any Calendar Quarter by more than [**] of the amounts otherwise due. Any deductions of a Xxxxxxxxx Portion to which AstraZeneca is entitled under this Section 5.6.1 may be carried forward to the next Calendar Quarter until fully exhausted.

5.6.2.Sublicensing of New Third Party Licenses. Such New Third Party License shall be (a) sublicensable to the Xxxxxxxxx for purposes of Xxxxxxxxx conducting activities or potential activities permitted under this Agreement and for performing obligations under this Agreement and (b) assignable to Xxxxxxxxx in the event of a termination of this Agreement. In the event AstraZeneca is unable to negotiate a New Third Party License that is sublicensable and assignable to Xxxxxxxxx to the extent set forth above, then the Parties will meet and discuss how to proceed.

0.0.0.Xxx Third Party Licenses Applicable only to Xxxxxxxxx. If any

intellectual property rights Controlled by a Third Party are necessary or useful only for Xxxxxxxxx to conduct activities or to perform obligations under this Agreement, then Xxxxxxxxx shall be free to enter into a New Third Party License for such intellectual property to Develop the applicable Collaboration Product anywhere in the world, solely for purposes of obtaining Regulatory Approval for such Collaboration Product.

5.7. Development Costs.

5.7.1.Definitions. As used in this Section 5.7, the following terms shall have

the following meanings.

(a)“China Basket Study Costs” means all Development Costs associated with the activities for the China Life Cycle Indication (3), the China Basket Study as described under Section 4.1.6 and Schedule 4.1.6.

(b)“China Development Activities” means (a) all Development activities relating to chemistry, manufacturing and control of the Collaboration Product and (b) all Development activities (other than Translational Research Activities) that (i) are conducted outside of China but are intended to directly support obtaining Regulatory Approval for a Collaboration Product in China, including the Phase I Clinical Trial for the Collaboration Product contemplated by the Parties on the Effective Date to be conducted in Australia, or (ii) are conducted inside of China.

(c)“China Life Cycle Indication Costs” means all Development Costs associated with the activities for the China Life Cycle Indications (1) and (2), the SACHI Study and Gastric Cancer Study as described under Section 4.1.6 and Schedule 4.1.6.

(d)“China Translational Costs” means all Translational Costs associated with Translational Research Activities that (i) are conducted outside of China but are principally related to obtaining Regulatory Approval for a Diagnostic Product in China or (ii) are conducted inside of China.

(e)“Development Costs” means all direct costs specifically identifiable or allocable to Development of a Collaboration Product and actually incurred by a Party or its Affiliates (it being understood that “direct costs” excludes overhead), including (a) reasonable costs of supplies and materials related to the foregoing and (b) reasonable amounts paid to Third Parties performing activities on behalf of such Party or its Affiliates, in all cases, to the extent such Development activities are specified in the Development Plan.

(f)“Global Translational Costs” means Translational Costs, other than China Translational Costs, associated with Translational Research Activities that are performed in support Regulatory Approval for a Diagnostic Product in the entire Territory.

(g)“Manufacturing Costs” means all direct costs specifically

identifiable or allocable to Manufacture of Collaboration Compound and Collaboration Product for use in China and actually incurred by a Party or its Affiliates (it being understood that “direct costs” excludes overhead), including (a) reasonable costs of supplies and materials related to the foregoing and (b) reasonable amounts paid to Third Parties performing activities on behalf of such Party or its Affiliates.

(h)“RCC Translational Costs” shall mean the Translational Costs which are required to detect a Met driven pathway based patient selection in the First RCC Phase III Clinical Trial or the Additional RCC Registrational Trials and which lead to the development and filing of a registration package for a diagnostic test based around the Met signalling pathway patient selection. For the avoidance of doubt, RCC Translational Costs are carved out from the costs defined in Section 5.7.1 (a)-5.7. 1(g).

(i)“First RCC Phase III Costs” shall mean [**], the actual amount of the costs for the First RCC Phase III Clinical Trial, such amount subject to audit by Xxxxxxxxx and reconciliation pursuant to Sections 5.8.7 through 5.8.9 mutatis mutandis. First RCC Phase III Costs shall include RCC Translational Costs. For the avoidance of doubt, First RCC Phase III Costs are carved out from the costs defined in Section 5.7.1(a)-5.7.1(g).

(j)“Additional RCC Phase III Costs” shall mean the actual costs for any registrational trials subsequent to the First RCC Phase III Clinical Trial (including the Second RCC Phase III Clinical Trial), set out in the Development Plan and Budget, except that, in the case of the Second RCC Phase III Clinical Trial only, FTEs shall be charged using a fixed-cost model of $2m per annum prorated for part of any year, and for so long as the trial continues but in any event for no longer than 3 years from first subject in to the Second RCC Phase III Clinical Trial. Additional RCC Phase III Costs shall include RCC Translational Costs. For the avoidance of doubt, Additional RCC Phase III Costs are carved out from the costs defined in Section 5.7.1(a)-5.7.1(g).

(k)“Shared Development Costs” means, subject to Section 5.7.2(f), (i) all Development Costs associated with China Development Activities and (ii) all costs associated with the Manufacture of Collaboration Compound and Collaboration Product for use in China.

(l)“Translational Costs” means all direct costs specifically identifiable or allocable to performance of the Translational Research Activities and actually incurred by a Party or its Affiliates (it being understood that “direct costs” excludes overhead), including (a) reasonable costs of supplies and materials related to the foregoing and (b) reasonable amounts paid to Third Parties performing activities on behalf of such Party or its Affiliates, in all cases, to the extent such Translational Research Activities are specified in the Development Plan.

(m)"Translational Costs Cap" means, with respect to amounts owed by Xxxxxxxxx in respect of the Global Translational Costs and the China Translational Costs pursuant to Section 5.7.3. an aggregate amount equal to [**].

5.7.2.Allocation of Development Costs.

(a)Subject to Sections 5.7.2(c), 5.7.2(d), 5.7.2(e), 5.7.2(f) and 5.7.2(f), Xxxxxxxxx shall be responsible for paying [**] of the Shared Development Costs, and AstraZeneca shall be responsible for paying [**] of the Shared Development Costs.

(b)[**].

(c)Xxxxxxxxx shall be responsible for (i) the First RCC Phase III Costs; (ii) the [**] of the costs of the Additional RCC Phase III Costs; and (iii) [**] of the Additional RCC' Phase III Costs provided always that: (aa) AstraZeneca shall track and calculate all such Additional RCC Phase III Costs incurred by it which shall be determined in accordance with IFRS and AstraZeneca shall keep a complete and accurate record of all such costs; (bb) within thirty (30) days after the end of each Calendar Quarter, AstraZenec a shall submit to Xxxxxxxxx a report setting forth in reasonable detail the Additional RCC Phase III Costs incurred by it during such Calendar Quarter, with an allocation of such costs between the Parties consistent with Articles 5.7.2(c) and 5.7.2(d) (hereafter, “Quarterly Cost Report”), along with such supporting documentation as Xxxxxxxxx may reasonably request. The Quarterly Cost Report shall include the latest estimates of development budget spending for the Additional RCC Registrational Trial based on the spend to date including analysis of actual spend and projected remaining amounts to be spent under such trial; (cc) Xxxxxxxxx shall reimburse AstraZeneca for Xxxxxxxxx'x allocation of the Additional RCC Phase III Costs within 30 days of receiving the Quarterly Cost Report; and (dd) AstraZeneca shall provide Xxxxxxxxx with such appropriate documentation to support the Quarterly Cost Report upon reasonable request from Xxxxxxxxx. although any such request by Xxxxxxxxx for additional documentation shall not delay or postpone Xxxxxxxxx'x obligation under (cc) to reimburse AstraZeneca within 30 days of receiving the Quarterly Cost Report.

(d)AstraZeneca shall be responsible for the [**] of the Additional RCC Phase III Costs referenced in Section 5.7.2(c).

(e)[**]

[**]

(f)Xxxxxxxxx shall be initially responsible for the China Life Cycle Indication Costs incurred on or before the Cut-off Date and, in the event that AstraZeneca:

(i)[**]

(ii)[**]

(g)Xxxxxxxxx shall be responsible for paying [**] of all China Basket Study Costs. After the exploratory phase of the China Basket Study is complete, and subject to the data on this exploratory phase of China Basket Study, Xxxxxxxxx will then come back to the JSC to seek approval for a Phase II study for the China Basket Study. If the Phase II study for the China Basket Study is approved by the JSC, the Development Costs relating to the Phase II study will be shared in accordance with Section 5.7.2(f) of this Agreement relating to China Life Cycle Indications.

(h)[**]

5.7.3.Allocation of Translational Costs.

(a)Subject to Section 5.7.3(c), and Section 5.7.2(c) and 5.7.2(d) Xxxxxxxxx shall be responsible for paying [**] of Global Translational Costs, and AstraZeneca shall be responsible for paying [**] of Global Translational Costs.

(b)Subject to Section 5.7.3(c), Xxxxxxxxx shall be responsible for

paying [**] of China Translational Costs, and AstraZeneca shall be responsible for paying [**] of China Translational Costs.

(c)Subject to Sections 5.7.2(c) and 5.7.2(d), notwithstanding anything to the contrary contained herein, in no event shall Xxxxxxxxx be obligated to make any out-of-pocket payments under Section 5.7.3(a) or 5.7.3(b) for the performance of Translational Research Activities that exceed, in the aggregate, the Translational Cost Cap. Any amounts owed by Xxxxxxxxx under such provisions that exceed the Translational Cost Cap, except for the RCC Translational Costs, may be deducted from the next applicable payment owed by AstraZeneca to Xxxxxxxxx under Section 5.2.1 or 5.2.2; provided, however, that any such deduction shall not reduce the amounts due to Xxxxxxxxx under Section 5.2.1 or 5.2.2 in any Calendar Quarter by more than [**] of the amounts otherwise due. Any deductions to which AstraZeneca is entitled under this Section 5.7.3(c) may be carried forward until fully exhausted.

5.7.4.Costs outside the Development Plan. [**].

5.8. Reports and Payments.

5.8.1.Royalty Reports. Within [**] days after the end of each Calendar Quarter beginning with the Calendar Quarter in which the First Commercial Sale is made in a country following receipt of Regulatory Approval in such country, AstraZeneca shall deliver to Xxxxxxxxx a report setting forth for the previous Calendar Quarter the following information on a Collaboration Product-by-Collaboration Product basis: (a) the Net Sales of each Collaboration Product in each country, (b) the number of units sold by Xxxxxxxxx, its Affiliates or Sublicensees, (c) the basis for any adjustments to the royalty payable for the sale of each Collaboration Product, (d) the royalty due hereunder for the sales of each Collaboration Product, and (e) the applicable exchange rate as determined in accordance with this Agreement. The total royalty due for the sale of Collaboration Products during such Calendar Quarter shall be remitted at [**]. No such reports shall be due for any Collaboration Product after the relevant Royalty Period for such Collaboration Product has expired.

5.8.2.Withholding Tax.

(a)[**]

[**].

(b)[**].

(c)[**].

(d)[**]

[**].

(e)[**].

(f)[**].

(g)[**].

(h)AstraZeneca represents and warrants that (i) it is resident in Sweden for tax purposes, and (ii) it is the beneficial owner of the payments which it is due to receive under this Agreement.

5.8.3.Indirect Taxes. Notwithstanding anything contained in Section 5.8.2, this Section 5.8.3 shall apply with respect to Indirect Taxes. All payments under this Agreement are stated exclusive of Indirect Taxes. If any Indirect Taxes are chargeable in respect of any Payments, the remitting Party shall pay Indirect Taxes at the applicable rate in respect of any such Payments following the receipt of an Indirect Taxes invoice in the appropriate form issued by receiving Party in respect of those payments, such Indirect Taxes to be payable on the later of the due date of the payment to which such Indirect Taxes relates and sixty (60) days after the receipt by the remitting Party of the applicable invoice relating to that Indirect Taxes payment. The Parties

shall issue invoices for all goods and services supplied under this Agreement consistent with Indirect Taxes requirements and irrespective of whether the sums may be netted for settlement purposes.

5.8.4.Currency. All amounts payable and calculations hereunder shall be in United States dollars. As applicable, Net Sales and any royalty deductions shall be translated into United States dollars in accordance with the paying Party’s customary and usual currency conversion procedures, consistently applied. If, due to restrictions or prohibitions imposed by national or international authority, payments cannot be made as provided in this Section 5, the Parties shall consult with a view to finding a prompt and acceptable solution, and the paying Party shall deal with such monies as the other Party may lawfully direct at no additional out-of-pocket expense to the paying Party.

5.8.5.Method of Payment. Except as permitted pursuant to Section 5.8.4, each payment hereunder shall be made by electronic transfer in immediately available funds via a bank wire transfer, an automated clearing house (ACH) mechanism or any other means of electronic funds transfer, at the paying Party’s election, to the bank account designed by the Party receiving payments under this Section 5 in writing to the paying Party at least thirty (30) days before the payment is due.

5.8.6.Record Keeping. AstraZeneca shall keep, and shall causes its Affiliates and Sublicensees to keep, books and accounts of record in connection with the Additional RCC Phase III Costs and the sale of Collaboration Products, including records of gross invoiced sales, Net Sales, exchange rates and royalty payments (collectively, the “Financial Records”), in accordance with IFRS or GAAP (as appropriate) and in sufficient detail to permit accurate determination of all figures necessary for verification of the Additional RCC Phase III Costs and royalties and Sales Milestone payments to be made by AstraZeneca under this Section 5. AstraZeneca and its Affiliates and Sublicensees shall maintain such records for a period of (i) at least three (3) years after the end of the Calendar Quarter in which they are generated or (ii) in the case of Additional RCC Phase III Costs, for one year after the end of such trial.

5.8.7.Audits. Upon thirty (30) days prior written notice from Xxxxxxxxx, AstraZeneca shall permit an independent certified public accounting firm of nationally recognized standing selected by Xxxxxxxxx and reasonably acceptable to AstraZeneca, to examine, at Xxxxxxxxx’x sole expense, the relevant Financial Records of AstraZeneca and its Affiliates and Sublicensees as may be reasonably necessary to verify the amounts reported by AstraZeneca in accordance with Sections 5.8.1 and 4.1.6(b)(1) and the royalties and Sales Milestone payments made by AstraZeneca in accordance with this Section 5 and the Additional RCC Phase III Costs. Xxxxxxxxx shall be entitled to conduct an audit in accordance with this Section 5.8.7 not more than once in any Calendar Year and such audit shall be limited to the pertinent Financial Records from any Calendar Year (i) ending not more than three (3) years prior to the date of the request; or (ii) in the case of audit of the Additional RCC Phase III Costs, from the commencement of the Additional RCC Registrational Trial. The accounting firm shall be provided access to such Financial Records at AstraZeneca’s facility(ies) where such Financial Records are normally kept and such audit shall be conducted during Astra Zeneca’s normal business hours. Upon completion of the audit, the accounting firm shall provide both Parties with a written report disclosing any discrepancies in the reports submitted by AstraZeneca or payments made by AstraZeneca or reimbursements of costs

made by Xxxxxxxxx, if any, and in each case, the specific details concerning any discrepancies. Any information provided by AstraZeneca to the accounting firm and the written report of the accounting firm shall be the Confidential Information of AstraZeneca.

5.8.8.Underpayments/Overpayments. If a report of an independent public accounting firm submitted to the Parties in accordance with Section 5.8.7 shows any underpayment of royalties and Sales Milestone payments due under this Section 5 or overpayment by Xxxxxxxxx of any Additional RCC Phase III Costs owed to AstraZeneca under Section 5.7, AstraZeneca shall remit to Xxxxxxxxx within [**] days after receipt of such report by AstraZeneca, (a) the amount of such underpayment or overpayment, as applicable and (b) if such underpayment exceeds [**] of the total amount owed to Xxxxxxxxx for the Calendar Year then being audited or if such overpayment exceeds [**] of the total amount of Additional RCC Phase III Costs actually owed by Xxxxxxxxx under Section 5.7 for the Calendar Year then being audited the reasonable fees and expenses of such independent public accounting firm performing the audit, subject to reasonable substantiation thereof. If such independent public accounting firm’s written report shows any overpayment of royalties and Sales Milestone payments due under this Section 5, AstraZeneca shall receive a credit equal to such overpayment against the royalties and Sales Milestone payments due under this Section 5 otherwise payable to Xxxxxxxxx.

5.8.9.Interest. Any payment under this Section 5 that is more than [**] days past due shall be subject to interest at an annual percentage rate of the Prime Rate (as published in the “Money Rates” table of the Eastern Edition of The Wall Street Journal during period such amount is overdue) plus [**] if Xxxxxxxxx does not make payment within [**] days of its receipt of notice that such amount is past due. Likewise, any overpayment that is not refunded within [**] days after the date such overpayment was made shall thereafter be subject to interest at an annual percentage rate of the Prime Rate (as published in the “Money Rates” table of the Eastern Edition of The Wall Street Journal during the period such amount is overdue) plus [**]; provided, however, that if the overpayment is due to errors in reports provided by AstraZeneca, such interest shall accrue from the date the overpayment was made. Notwithstanding the preceding, if a Party contests any amounts due hereunder in good faith and promptly notifies the other Party of such dispute, interest shall not accrue as to amounts being so contested until [**] days following the presentation of such notice to the other Party.

6.COVENANTS.

6.1. Confidentiality.

6.1.1.Confidential Information. Except to the extent expressly permitted by this Agreement and subject to the provisions of Sections 6.1.2 and 6.1.3, at all times during the Term and for five (5) years following the expiration or termination hereof, each Party (the “Receiving Party”) receiving any Confidential Information of the other Party (the “Disclosing Party”) in connection with this Agreement shall: (a) keep completely confidential and shall not publish or otherwise disclose any Confidential Information furnished to it by the Disclosing Party, except to those of the Receiving Party’s employees, Affiliates, consultants or representatives who have a need to know such information (collectively, “Recipients”) to perform such Party’s obligations or exercising its rights hereunder and (b) shall not use Confidential Information of the

Disclosing Party directly or indirectly for any purpose other than performing its obligations or exercising its rights hereunder. The Receiving Party shall be liable for any breach by any of its Recipients of the restrictions set forth in this Agreement. Notwithstanding the foregoing, in no event, except as permitted under Section 6.1.3, shall Xxxxxxxxx disclose any Confidential Information relating to the Collaboration Compound or Collaboration Product to any party that becomes an Affiliate of Xxxxxxxxx as a result of a Change of Control without the prior written consent of AstraZeneca.

6.1.2.Exceptions to Confidentiality. The Receiving Party’s obligations set forth in this Section shall not extend to any Confidential Information of the Disclosing Party:

(a)that is or hereafter becomes part of the public domain through no wrongful act, fault or negligence on the part of a Receiving Party or its Recipients;

(b)that is received from a Third Party without restriction and without breach of any agreement or fiduciary duty between such Third Party and the Disclosing Party;

(c)that the Receiving Party can demonstrate by competent evidence was already in its possession without any limitation or restriction on use or disclosure prior to its receipt from the Disclosing Party;

(d)that is generally made available to Third Parties by the Disclosing Party without any restriction imposed by the Disclosing Party on disclosure, whether such restriction is by contract, fiduciary duty or by operation of law; or

(e)that the Receiving Party can demonstrate by competent evidence was independently developed by the Receiving Party without any reference to Confidential Information.

6.1.3.Authorized Disclosure. Notwithstanding the provisions of Section 6.1.1, the Receiving Party and its Recipients may disclose Confidential Information belonging to the Disclosing Party to the extent that such disclosure is reasonably necessary to:

(a)Prosecute or defend litigation;

(b)Comply with applicable governmental laws and regulations (including applicable law, rule or regulation or the requirements of a national securities exchange or another similar regulatory body);

(c)Make filings and submissions to, or correspond or communicate with, any Government Authority.

In the event that the Receiving Party or its Recipients, as applicable, deem it reasonably necessary to disclose Confidential Information belonging to the Disclosing Party pursuant to this Section 6.1.3, the Receiving Party shall, to the extent possible, provide the Disclosing Party with reasonable advance notice of such disclosure and take reasonable measures (including for

example, where appropriate, the filing of a redacted copy of this Agreement approved by both Parties) to ensure confidential treatment of such information. In addition, the Receiving Party may disclose Confidential Information belonging to the Disclosing Party to any Third Party who is performing diligence in connection with a transaction with the Receiving Party (including potential Sublicensees and licensees) and to any Third Party performing work contemplated by this Agreement; provided that, each such Third Party has signed a written confidentiality agreement with the Receiving Party that is no less restrictive than the terms hereof.

6.1.4.Notification. The Receiving Party shall notify the Disclosing Party immediately, and cooperate with the Disclosing Party as the Disclosing Party may reasonably request, upon the Receiving Party’s discovery of any loss or compromise of the Disclosing Party’s Confidential Information.

6.1.5.Destruction of Confidential Information. Upon the expiration or earlier termination of this Agreement, except with respect to Confidential Information necessary or useful for a Receiving Party to exercise any rights or perform any obligations under this Agreement surviving such expiration or termination, the Receiving Party shall (a) destroy all tangible embodiments of Confidential Information of the Disclosing Party, including any and all copies thereof, and those portions of any documents, memoranda, notes, studies and analyses prepared by the Receiving Party or its Recipients that contain, incorporate or are derived from such Confidential Information and provide written certification of such destruction to the Disclosing Party in a form reasonably acceptable to the Disclosing Party, provided that the legal department of the Receiving Party shall have the right to retain one (1) copy of any such tangible embodiments for archival purposes, provided such copy shall continue to be maintained on a confidential basis subject to the terms of this Agreement, and (b) immediately cease, and shall cause its Recipients to cease, use of such Confidential Information as well as any information or materials that contain, incorporate or are derived from such Confidential Information.

6.1.6.Use of Name and Disclosure of Terms. Each Party shall keep the existence of, the terms of and the transactions covered by this Agreement confidential and shall not disclose such information to any Third Party through a press release or otherwise, or mention or otherwise use the name, insignia, symbol, trademark, trade name or logotype of the other Party or its Affiliates in any manner without the prior written consent of the other Party in each instance (which shall not be unreasonably withheld); provided, however, that a Receiving Party may disclose such information without the prior consent of the Disclosing Party to any Third Party who is performing diligence in connection with a transaction with such Receiving Party (including potential Sublicensees and licensees) so long as each such Third Party has signed a written confidentiality agreement with such Receiving Party no less restrictive than the terms hereof. The restrictions imposed by this Section 6.1.6 shall not prohibit either Party from making any disclosure that is required by applicable law, rule or regulation or the requirements of a national securities exchange or another similar regulatory body, including disclosing such information in any clinical trial database maintained by or on behalf of a Party, or that is expressly permitted under this Agreement. Further, the restrictions imposed on each Party under this Section 6.1.6 are not intended, and shall not be construed, to prohibit a Party from identifying the other Party in its internal business communications, provided that any Confidential Information in such communications remains subject to this Section 6.1.6.

6.1.7.Remedies. The Parties acknowledge and agree that the restrictions set forth in Section 6.1 are reasonable and necessary to protect the legitimate interests of the Parties and that neither Party would have entered into this Agreement in the absence of such restrictions, and that any breach or threatened breach of any provision of Section 6.1 will result in irreparable injury to the other Party for which there will be no adequate remedy at law. In the event of a breach or threatened breach of any provision of Section 6.1 by a Party, the other Party shall be authorized and entitled to obtain from any court of competent jurisdiction injunctive relief, whether preliminary or permanent, specific performance and an equitable accounting of all earnings, profits and other benefits arising from such breach, which rights shall be cumulative and in addition to any other rights or remedies to which such Party may be entitled in law or equity. The breaching Party agrees to waive any requirement that the non-breaching Party (a) post a bond or other security as a condition for obtaining any such relief and (b) show irreparable harm, balancing of xxxxx, consideration of the public interest or inadequacy of monetary damages as a remedy. Nothing in this Section 6.1.7 is intended, or shall be construed, to limit the Parties’ rights to equitable relief or any other remedy for a breach of any provision of this Agreement.

6.2. Compliance with Law. Each Party hereby covenants and agrees to comply with all laws applicable to its activities connected with the Development, Manufacture and Commercialization (as applicable) of Collaboration Products. Without limiting the generality of the foregoing:

6.2.1.Patient Information. Each Party agrees to abide by all laws, rules, regulations, and orders of all applicable supranational, national, federal, state, provincial, and local governmental entities concerning the confidentiality or protection of patient identifiable information or patients’ protected health information in the course of their performance under this Agreement.

6.2.2.Export Controls. This Agreement is made subject to any restrictions concerning the export of products or technical information from the United States or other countries which may be imposed upon or related to Xxxxxxxxx or AstraZeneca from time to time. Each Party agrees that it shall not export, directly or indirectly, any technical information acquired from the other Party pursuant to this Agreement or any Collaboration Products using such technical information to a location or in a manner that at the time of export requires an export license or other governmental approval, without first obtaining the written consent to do so from the appropriate agency or other governmental entity.

6.2.3.Debarment. Each Party agrees that it shall not knowingly use, in any capacity, in connection with any of its obligations to be performed under this Agreement any individual who has been disqualified or debarred by the United States Food and Drug Administration, pursuant to 21 U.S.C. §§ 335(a) or (b), or been charged with or convicted under United States law for conduct relating to the development or approval, or otherwise relating to the regulation of Collaboration Product under the Generic Drug Enforcement Act of 1992, or any other relevant law, rule, or regulation or been disbarred, disqualified, or convicted under or for any equivalent or similar applicable foreign law, rule, or regulation.

6.3. Anti-Corruption Laws.

6.3.1.Compliance with Anti-Corruption Law. In carrying out their responsibilities under this Agreement, the Parties shall comply with all applicable anti-corruption laws in the countries where the Parties have their principal or other places of business and where they conduct activities under this Agreement. Additionally, the Parties understand and agree to comply with the U.S. Foreign Corrupt Practices Act of 1977 (“US Act”) and the UK Bribery Act of 2010 (“UK Act”), in each case as revised, which in the case of the US Act generally prohibits the promise, payment or giving of anything of value either directly or indirectly to any government official for the purpose of obtaining or retaining business or any improper advantage, and in the case of the UK Act includes the prohibition on the making of any bribe to a foreign public official with the intention of influencing such person in order to obtain or retain business or an advantage in the conduct of business. For purposes of this section, (a) “government official” means any official, officer, representative, or employee of, including any doctor employed by, any non-U.S. government department, agency or instrumentality (including any government-owned or controlled commercial enterprise), or any official of a public international organization or political party or candidate for political office; and (b) “foreign public official” means an individual who holds a legislative, administrative or judicial position of any kind, whether appointed or elected, of a country or territory outside the United Kingdom (or any subdivision of such a country or territory); exercises a public function (i) for or on behalf of a country or territory outside the United Kingdom (or any subdivision of such a country or territory), or (ii) for any public agency or public enterprise of that country or territory (or subdivision); or is an official or agent of a public international organization.

6.3.2.Certain Covenants regarding Anti-Corruption. Additionally, each Party represents and warrants to the other Party that neither it nor any of its, directors, employees, agents, consultants (or any other person who may be associated with a Party for the purposes of the UK Act) will directly or indirectly pay or give or promise to pay or give anything of value to any government official or a foreign public official for purposes of (a) influencing any act or decision of any such person in his official capacity; (b) inducing such person to do or omit to do any act in violation of the lawful duty of such official; (c) securing any improper advantage; or (d) inducing such person to use his position to affect or influence any act or decision of government or any legislative, administrative, public agency or other public body with respect to any activities undertaken relating to this Agreement. Additionally, the Parties will make reasonable efforts to comply with requests for information, including answering questionnaires and narrowly tailored audit inquiries, to enable the other Party to ensure compliance with any applicable anti-corruption laws.

6.3.3.Breach of Anti-Corruption Covenants. The Parties agree that a breach of the anti-corruption commitments in Section 6.3 shall be considered a material breach of this Agreement and that either Party may immediately seek all remedies available under law and equity including termination of this Agreement pursuant to Section 10.3.1 if it believes, in good faith, that the covenants under the anti-corruption commitments in this Section 6.3 have been breached by the other Party, without owing to the other any damages or indemnification resulting solely from such termination.

6.4. Exclusivity.

6.4.1.Scope of Exclusivity. Each Party agrees that, from the Effective Date

until the earlier of (x) [**] and (y) the date that is [**] years after the Effective Date (the “Exclusivity Period”), the following restrictions shall apply:

(a)Neither Party nor its Affiliates or Sublicensees shall,directly or indirectly, Develop, Manufacture or Commercialize any Collaboration Compound, except as set forth in the Development Plan or as otherwise set forth herein.

(b)Except as expressly permitted under this Section 6.4, neither Party shall develop, manufacture or commercialize any Agreement Compound, independently or for or with any of its Affiliates or any Third Party (including through the grant of any license to any Third Party); provided, however, [**]. For the avoidance of doubt, in no event shall either Party conduct any Clinical Trial of any Agreement Compound, including any Back-Up Compound, without the prior written consent of the other Party.

6.4.2.Acquisition of Agreement Compound. A Party will not be deemed to be in breach of the restrictions set forth in Section 6.4.1(b) if such Party or any of its Affiliates acquires, through an acquisition of or a merger with the whole or substantially the whole of the business or assets of another Person, an Agreement Compound that such Person is developing in the clinic, manufacturing or commercializing, independently or for or with any of its Affiliates or any Third Party (including though the grant of a license to any Third Party) (such activities, the “Restricted Activities”), so long as such Party (or its Affiliate) [**]. As used in this Section 6.4.2, the following terms shall have the following meanings.

(a)“Hold Separate Transaction” means any “hold separate” transaction (whether through the establishment of a trust or otherwise) involving the proposed sale of an Agreement Compound pursuant to an agreement with any Government Authority responsible for antitrust laws.

(b)“Divest” or “Divestiture” means, with respect to any Agreement Compound, (i) the sale, exclusive license or other transfer of all of the right, title and interest in and to such Agreement Compound, including all technology, intellectual property and other assets relating solely thereto, to an independent Third Party, without the retention or reservation of any rights, license or interest (other than customary residual rights in the event of a termination) in such Agreement Compound and (ii) the complete shutdown of the Agreement Compound such that no technology, intellectual property or other asset relating thereto is used by the applicable Party or its Affiliates and delivery of written confirmation from such Party to the other Party that such Party and its Affiliates covenant not to use any technology, intellectual

property and assets solely relating to such Agreement Compound during the Exclusivity Period.

6.4.3.Breach of Exclusivity. If, at any time during the Exclusivity Period, a Party is in breach of the restrictions set forth in Section 6.4.1(b), then the other Party shall have the right to terminate this Agreement immediately upon providing written notice of such termination, in which case the effects of termination set forth in Section 10.4.2 shall apply.

6.5. Change of Control.

6.5.1.Notice. In the event of any Change of Control that occurs during the Term, Xxxxxxxxx shall notify AstraZeneca promptly thereof, but in no event later than [**] Business Days following execution of the definitive agreement contemplating the transaction that would constitute such Change of Control. Upon receipt of such notice, AstraZeneca shall have the right, by submitting written notice to Xxxxxxxxx no later than [**] days after the closing of such Change of Control (such notice, the “COC Amendment Notice”), to amend this Agreement in accordance with the terms and conditions set forth in Sections 6.5.2 and 6.5.3 (such amendment, a “COC Amendment”). In the event that AstraZeneca submits a COC Amendment Notice, the Parties will enter into an appropriate and customary written amendment reflecting the terms and conditions set forth in Sections 6.5.2 and 6.5.3.

6.5.2.Change of Control before [**]. Where a Change of Control occurs at any time prior [**], any COC Amendment shall contain the following terms:

(a)[**]

(b)[**]

(c)[**]

[**]

(d)[**]

(e)[**]

(f)[**]

(g)[**]

(h)[**]

6.5.3.Change of Control after [**]. Where a Change of Control occurs at any time after the [**], any COC Amendment shall contain the following terms:

(a)Xxxxxxxxx shall, and hereby does, assign to AstraZeneca all right, title and interest in and to: (i) Xxxxxxxxx Patent Rights and Joint Patent Rights, all Regulatory Submissions and Regulatory Approvals Controlled by Xxxxxxxxx or any Affiliate pertaining to Collaboration Compound, Collaboration Product and Diagnostic Products in the Field in the Territory and (ii) all of [**];

(b)[**]

(c)[**]

(d)[**]

(e)[**]

(f)[**]

(g)[**]

(h)[**]

6.6. Non-Solicitation. During the Term, neither Party nor any of its Affiliates shall, directly or indirectly, anywhere in the Territory solicit for employment, any person engaged in the Development, Manufacture or Commercialization of any Collaboration Compound or Collaboration Product employed by either Party or their Affiliates, during the period such person is so employed or for [**] after termination of such person’s employment provided that such restriction shall not apply in the case where such employee responds to an advertisement of employment made by either Party in the normal course of their business.

7.REPRESENTATIONS AND WARRANTIES.

7.1. Representations and Warranties of Each Party. As of the Effective Date, each of AstraZeneca and Xxxxxxxxx hereby represents and warrants to the other Party hereto as follows:

0.0.0.xx is a corporation or entity duly organized and validly existing under the laws of the state or other jurisdiction of its incorporation or formation;

7.1.2.the execution, delivery and performance of this Agreement by such Party has been duly authorized by all requisite corporate action and does not require any shareholder action or approval;

0.0.0.xx has the power and authority to execute and deliver this Agreement and to perform its obligations hereunder;

7.1.4.the execution, delivery and performance by such Party of this Agreement and its compliance with the terms and provisions does not and shall not conflict with or result in a breach of any of the terms and provisions of or constitute a default under (i) a loan agreement, guaranty, financing agreement, agreement affecting a product or other agreement or instrument binding or affecting it or its property; (ii) the provisions of its charter or operative documents or bylaws; or (iii) any order, writ, injunction or decree of any court or governmental authority entered against it or by which any of its property is bound; and

0.0.0.xx has the full right, power and authority to grant all of the right, title and interest in the licenses granted to the other Party under this Agreement.

7.2. Additional Representations and Warranties of Xxxxxxxxx. Xxxxxxxxx hereby represents and warrants to AstraZeneca that as of the Effective Date:

7.2.1.Xxxxxxxxx, together with its Affiliates, is the sole and exclusive owner of, and has the sole right, title and interest in and to, the Xxxxxxxxx Patent Rights and the Xxxxxxxxx Know-How, in each case free and clear of any mortgage, pledge, claim, security interest, covenant, easement, encumbrance, lien, lease, sublease, option, or charge of any kind, limitations on transfer or any subordination arrangement in favor of a Third Party;

7.2.2.All of the Xxxxxxxxx Patent Rights listed on Schedule 1.49 are in force or pending and have not been abandoned as of the Effective Date, and to Xxxxxxxxx’x knowledge, all such Xxxxxxxxx Patent Rights are valid and enforceable;

0.0.0.Xx Third Party has challenged or has threatened in writing to challenge the extent, validity or enforceability of the patents encompassed within the Xxxxxxxxx Technology relating to the Collaboration Compound (including, by way of example, through the institution or written threat of institution of interference, nullity or similar invalidity proceedings before the US Patent and Trademark Office or any analogous foreign entity), and to the knowledge of Xxxxxxxxx, all application, registration, maintenance and renewal fees in respect of Xxxxxxxxx Patent Rights have been paid and all documents and certificates required to be filed with the relevant agencies for the purpose of maintaining such Xxxxxxxxx Patent Rights have been filed;

7.2.4.Neither Xxxxxxxxx nor any of its Affiliates has granted any license, option or other rights of any kind to or in favor of a Third Party under the Xxxxxxxxx Technology;

7.2.5.There is no intellectual property right, and in particular no Patent Right, owned or Controlled by Xxxxxxxxx or its Affiliates other than the Xxxxxxxxx Technology, that is

necessary for AstraZeneca or its Affiliates and subcontractors to Develop a Collaboration Compound as set forth herein;

0.0.0.Xx Xxxxxxxxx’x knowledge, the manufacture, use, sale, offer for sale and importation of the Collaboration Compound in the Field in the Territory, in the form in which it is being Developed by Xxxxxxxxx as of the Effective Date, does not infringe any Patent Rights of a Third Party;

7.2.7.There are no claims, judgments or settlements pending against Xxxxxxxxx or its Affiliates with respect to any Xxxxxxxxx Technology, and Xxxxxxxxx has not received notice that any such claims, judgments or settlements are threatened; and

7.2.8.All employee inventions relevant to the rights granted to AstraZeneca under this Agreement have been duly transferred to Xxxxxxxxx or its Affiliates in accordance with Applicable Law or Xxxxxxxxx has entered into binding agreements permitting such a transfer; and

7.2.9.Xxxxxxxxx has heretofore disclosed or made available to AstraZeneca all material scientific and technical information and all material information relating to safety and efficacy known to it or its Affiliates with respect to the Collaboration Compound and has made available to AstraZeneca complete and accurate copies of all material documentation and correspondence submitted to or received from any Regulatory Authority with respect to the Collaboration Compound.

7.3. Representation by Legal Counsel. Each Party hereto represents that it has been represented by legal counsel in connection with this Agreement and acknowledges that it has participated in the drafting. In interpreting and applying the terms and provisions of this Agreement, the Parties agree that no presumption shall exist or be implied against the Party which drafted such terms and provisions.

7.4. No Inconsistent Agreements. Neither Party has in effect and after the Effective Date neither Party shall enter into any oral or written agreement or arrangement that would be inconsistent with its obligations under this Agreement or limit the ability of either Party to grant the licenses set forth in Section 2 of this Agreement.

7.5. Disclaimer. THE FOREGOING WARRANTIES OF EACH PARTY ARE IN LIEU OF ANY OTHER WARRANTIES, EXPRESS OR IMPLIED, INCLUDING ANY IMPLIED WARRANTIES OF NONINFRINGEMENT, ANY IMPLIED WARRANTIES OF MERCHANTABILITY OR ANY IMPLIED WARRANTIES OF FITNESS FOR A PARTICULAR PURPOSE ALL OF WHICH ARE HEREBY SPECIFICALLY EXCLUDED AND DISCLAIMED. EACH PARTY HEREBY DISCLAIMS ANY REPRESENTATION OR WARRANTY THAT THE DEVELOPMENT, MANUFACTURE OR COMMERCIALIZATION OF ANY PRODUCT UNDER THIS AGREEMENT WILL BE SUCCESSFUL.

8. INTELLECTUAL PROPERTY.

8.1. Disclosure. During the Term, the Parties shall promptly disclose to one another all Collaboration Know-How (whether patentable or not).

8.2. Ownership.

8.2.1.Ownership of Technology. Determinations as to which Party has Invented any Patent Right or Know-How shall be made in accordance with the standards of inventorship under the patent laws of the United States. Subject to the license grants under Section 2 of this Agreement, as between the Parties, [**]. Neither Party shall take any action that would limit the other Party’s right to exercise its rights under Section 2.4. In the event inventorship and ownership of any Collaboration Technology cannot be resolved by the Parties with advice of their respective intellectual property counsel, such dispute shall be resolved through the dispute resolution mechanism set forth in Section 12.1.

8.2.2.Employee Assignment. To the extent permissible under Applicable Laws, each Party will cause each employee and contractor conducting work on such Party’s behalf under this Agreement to sign a contract that (a) compels prompt disclosure to the Party of all Xxxxxxxxx Technology, AstraZeneca Technology, and Joint Technology, as applicable, conceived or reduced to practice by such employee or contractor during any performance under this Agreement, (b) automatically assigns to the Party all right, title and interest in and to all such Technology and all Patent Rights disclosing or claiming such Technology and (c) obligates such persons to similar obligations of confidentiality as set forth in this Agreement. Each Party will require each employee and contractor conducting work on such Party’s behalf under this Agreement to maintain records in sufficient detail and in a good scientific manner appropriate for patent purposes to properly reflect all work done. Each Party shall be responsible for the payment of any remuneration due to employees under any Applicable Law which provides compensation to such employee inventors.

8.3. JIPC. The JIPC shall, from time to time, review and discuss the patent strategy for inventions made in the course of the Development and to coordinate patent strategy relating to the Collaboration Patent Rights, to the extent such Collaboration Patent rights are necessary or useful to Manufacture, Develop or Commercialize a Collaboration Compound or Collaboration Product.

8.4. Filing, Prosecution and Maintenance of Patent Rights.

8.4.1.Xxxxxxxxx Patent Rights. AstraZeneca shall be responsible, at its sole cost and expense, for the preparation, filing and prosecution and maintenance of the Xxxxxxxxx Patent Rights in the Territory. If AstraZeneca or its Affiliates use any of its employees to conduct any preparation, prosecution or maintenance activity under this Agreement, then neither AstraZeneca nor any Affiliate shall be liable to Xxxxxxxxx in respect of any act or omission in undertaking such activity. In the event external counsel are used then no such exclusion of liability shall apply. AstraZeneca shall keep Xxxxxxxxx advised on the status of preparation, filing, prosecution and maintenance of all patent applications included within the Xxxxxxxxx Patent Rights and the maintenance of any issued patents within the Xxxxxxxxx Patent Rights. Further, AstraZeneca shall consult and reasonably cooperate with Xxxxxxxxx with respect to the preparation, filing, prosecution and maintenance of all Xxxxxxxxx Patent Rights, including: (a) allowing Xxxxxxxxx a reasonable opportunity and reasonable time to review and comment regarding relevant

material communications and drafts of any material responses or proposed filings by AstraZeneca before any applicable filings are submitted to any relevant patent office or Government Authority and (b) reflecting any reasonable comments offered by Xxxxxxxxx in any final filings submitted by AstraZeneca to any relevant patent office or Governmental Authority.

8.4.2.AstraZeneca Patent Rights. AstraZeneca shall have the sole and exclusive right to prepare, file, prosecute and maintain the AstraZeneca Patent Rights in the Territory, in its sole discretion.

8.4.3.Joint Patent Rights. AstraZeneca shall be responsible, at its sole cost and expense, for the preparation, filing and prosecution and maintenance of the Joint Patent Rights in the Territory. If AstraZeneca or its Affiliates use any of its employees to conduct any preparation, prosecution or maintenance activity under this Agreement, then neither AstraZeneca nor any Affiliate shall be liable to Xxxxxxxxx in respect of any act or omission in undertaking such activity. In the event external counsel are used no such exclusion of liability shall apply. AstraZeneca shall keep Xxxxxxxxx advised on the status of preparation, filing, prosecution and maintenance of all patent applications included within the Joint Patent Rights and the maintenance of any issued patents within the Joint Patent Rights. Further, AstraZeneca shall consult and reasonably cooperate with Xxxxxxxxx with respect to the preparation, filing, prosecution and maintenance of all Joint Patent Rights, including: (a) allowing Xxxxxxxxx a reasonable opportunity and reasonable time to review and comment regarding relevant material communications and drafts of any material responses or proposed filings by AstraZeneca before any applicable filings are submitted to any relevant patent office or Government Authority and (b) reflecting any reasonable comments offered by Xxxxxxxxx in any final filings submitted by AstraZeneca to any relevant patent office or Governmental Authority.

8.4.4.Reversion Rights. If AstraZeneca decides not to file, prosecute or maintain any Patent Right under Section 8.4.1 or 8.4.3, it shall give Xxxxxxxxx reasonable notice to that effect sufficiently in advance of any deadline for any filing with respect to such Patent Right so as to permit Xxxxxxxxx to carry out such activity. Upon delivery of such notice, Xxxxxxxxx shall have the right to file, prosecute and maintain such Patent Right, and AstraZeneca shall perform such acts as may be reasonably necessary for Xxxxxxxxx to file, prosecute or maintain such Patent Right, at Xxxxxxxxx’x sole cost and expense. If Xxxxxxxxx does so elect, then AstraZeneca shall provide such cooperation to Xxxxxxxxx, including the execution and filing of appropriate instruments, as may reasonably be requested to facilitate the transition of such patent activities, and shall assign all of its right, title and interest to such Patent Right to Xxxxxxxxx. Any such Patent Right abandoned by AstraZeneca under Section 8.4.1 or 8.4.3 shall be deemed to be excluded from the Xxxxxxxxx Patent Rights or Joint Patent Rights, as applicable, and shall thereafter cease to be included within the scope of the licenses granted to AstraZeneca under Section 2.

8.4.5.Patent Term Extensions. The Parties shall cooperate, if necessary and appropriate, with each other in gaining patent term extensions, including supplementary protection certificates and any other extensions that are now or become available in the future wherever applicable to Patent Rights that are applicable to the Collaboration Products. The Parties shall, if necessary and appropriate, use reasonable efforts to agree upon a joint strategy relating to patent term extensions, but, in the absence of mutual agreement with respect to any extension issue, a Patent Right shall be extended only as and if AstraZeneca elects to extend such Patent Right. All

filings for such extension shall be made by AstraZeneca.

0.0.0.Xxxxxx Book Listing. Xxxxxxxxx shall, at AstraZeneca’s expense and upon AstraZeneca’s reasonable request, (a) provide all necessary or reasonably useful information to enable AstraZeneca to make filings with Regulatory Authorities with respect to Xxxxxxxxx Patent Rights or Joint Patent Rights as required (i) in the United States for the FDA’s Orange Book and (ii) outside the United States under other international equivalents and (b) shall cooperate with AstraZeneca in connection therewith, including meeting any submission deadlines.

8.4.7.Costs and Expenses. [**].

8.5. Trademarks.

8.5.1.Collaboration Product Trademarks. AstraZeneca shall select and own the Trademarks for the Collaboration Products and shall be solely responsible for applying for and maintaining the registrations for the Trademarks throughout the Territory, and all goodwill associated therewith will inure to the benefit of AstraZeneca. AstraZeneca shall bear all costs of applying for and maintaining registrations for the Trademarks. AstraZeneca shall assume full responsibility, at its sole costs and expense, for prosecuting any infringement of a Trademark by a Third Party, and shall be entitled to retain all recoveries in connection therewith. AstraZeneca shall own the Trademarks, and all applications and registrations therefor.

8.6. Enforcement of Technology Rights.

8.6.1.Notice. Each Party will promptly notify the other in the event of any actual, potential or suspected infringement of a patent under the Xxxxxxxxx Patent Rights or the Joint Patent Rights by any Third Party (an “Infringement”).

8.6.2.Enforcement. As between AstraZeneca and Xxxxxxxxx, AstraZeneca shall have the first right, except as otherwise provided in this Section 8.6.2, but not the obligation, to institute litigation or take other steps to remedy an Infringement, and any such litigation or steps shall be at AstraZeneca’s expense subject to Xxxxxxxxx’x obligation to indemnify AstraZeneca for such expenses pursuant to Section 11.1, provided that, any recoveries resulting from such litigation or steps relating to a claim of Infringement, after deducting AstraZeneca’s out of pocket expenses (including counsel fees and expenses) in pursuing such claim, will be deemed Net Sales of AstraZeneca. AstraZeneca shall have full control of such litigation or steps but shall not, without the prior written consent of Xxxxxxxxx, enter into any compromise or settlement relating to such litigation that (a) admits the invalidity or unenforceability of any Xxxxxxxxx Patent Right or Joint Patent Right or (b) requires AstraZeneca to abandon any Xxxxxxxxx Patent Right or Joint Patent Right. In order to establish standing, Xxxxxxxxx, upon request of AstraZeneca, agrees to timely commence or to join in any such litigation, at AstraZeneca’s expense, and in any event to cooperate with AstraZeneca in such litigation or steps at AstraZeneca’s expense. Xxxxxxxxx shall have the right to consult with AstraZeneca about such litigation and to participate in and be represented by independent counsel in such litigation at Xxxxxxxxx’x own expense. If AstraZeneca fails to institute such litigation or otherwise take steps to remedy an Infringement of any Xxxxxxxxx Patent Right or

Joint Patent Right within [**] days of its receipt of notice thereof, then Xxxxxxxxx shall have the right, but not the obligation, upon [**] days’ prior notice to AstraZeneca, at Xxxxxxxxx’x expense, to institute any such litigation and any proceeds from such litigation shall be retained by Xxxxxxxxx. AstraZeneca shall, at Xxxxxxxxx’x expense, cooperate with Xxxxxxxxx in any such litigation. Neither Party shall incur any liability to the other Party as a consequence of any litigation initiated or pursued pursuant to this Section 8.6.2 or any unfavorable decision resulting therefrom, including any decision holding any Xxxxxxxxx Patent Right or Joint Patent Right invalid or unenforceable.

8.7. Third Party Claims.

8.7.1.Third Party Claims – Course of Action. If the Development, Commercialization or Manufacture of a Collaboration Product under this Agreement is alleged by a Third Party to infringe a Third Party’s Patent Right(s) or misappropriate a Third Party’s trade secret, the Party becoming aware of such allegation shall promptly notify the other Party thereof, in writing, reasonably detailing the claim.

8.7.2.Third Party Suit. If a Third Party sues a Party (the “Sued Party”) alleging that the Sued Party’s or the Sued Party’s Sublicensees’ Development, Manufacture or Commercialization of the Collaboration Compound or Collaboration Product infringes or shall infringe said Third Party’s Patent Right(s) or misappropriates said Third Party’s trade secret, [**] to defend or settle such claim in its own name after consultation with Xxxxxxxxx and in connection with its defense of any such Third Party suit, Xxxxxxxxx shall provide reasonable assistance to AstraZeneca for such defense and shall join such suit if deemed a necessary party. AstraZeneca shall keep Xxxxxxxxx, if Xxxxxxxxx has not joined in such suit, reasonably informed on a quarterly basis, in person or by telephone, prior to and during the pendency of any such suit. AstraZeneca shall not admit the invalidity of any patent within the Xxxxxxxxx Patent Rights, the AstraZeneca Patent Rights or the Joint Patent Rights, nor settle any such suit, without written consent of the other Party, such consent not to be unreasonably withheld or delayed. Subject to Xxxxxxxxx’x indemnity obligations pursuant to Section 11.1, all litigation expenses, including settlement costs, royalties paid in settlement of any such suit, and the payment of any damages to the Third Party will be paid by AstraZeneca.

8.8. Patent Certifications. Each Party shall immediately give written notice to the other of any certification of which it becomes aware has been filed pursuant to 21 U.S.C. § 355(b)(2)(A), or § 355(j)(2)(A)(vii) or any amendment or successor statute thereto or any analog in any other jurisdiction claiming that the Xxxxxxxxx Patent Rights or Joint Patent Rights covering a Collaboration Product are invalid or that infringement shall not arise from the manufacture, use, import sale or offer for sale of such Third Party product by a Third Party. AstraZeneca shall have the right, in the first instance, to commence an ANDA Proceeding in connection with any such certification. If AstraZeneca decides not to bring infringement proceedings against the Third Party making such a certification with respect to any Collaboration Product, AstraZeneca will give notice to Xxxxxxxxx of its decision not to bring suit within [**] business days after receipt of notice of such certification (or, if the time period permitted by law is less than [**] business days, within half of the time period permitted by law for AstraZeneca to commence such action) and Xxxxxxxxx may then,

but shall not be obligated to, bring suit against the Third Party that filed the certification. Any suit by either Party may be in the name of either or both Parties, as may be required by law. For this purpose, the Party not bringing suit will execute such legal papers necessary for the prosecution of such suit as may be reasonably requested by the Party bringing suit.

8.9. No Implied Licenses. Except as expressly set forth in this Agreement, no right or license under any Xxxxxxxxx Technology or AstraZeneca Technology is granted or shall be granted by implication as a result of the respective rights of the Parties under this Agreement. All such rights or licenses are or shall be granted only as expressly provided in this Agreement.

8.10.Privileged Communications. In furtherance of this Agreement, it is expected that AstraZeneca and Xxxxxxxxx will, from time to time, disclose to one another privileged communications with counsel, including opinions, memoranda, letters and other written, electronic and verbal communications. Such disclosures are made with the understanding that they shall remain confidential, they will not be deemed to waive any applicable attorney-client privilege and that they are made in connection with the shared community of legal interests existing between Xxxxxxxxx and AstraZeneca, including the community of legal interests in avoiding infringement of any valid, enforceable patents of Third Parties and maintaining the validity of Xxxxxxxxx Patent Rights, AstraZeneca Patent Rights and Joint Patent Rights.

8.11.Create Act. This Agreement includes a joint research agreement as defined in 35 U.S.C. § 103(c)(3). Notwithstanding anything to the contrary in this Article 8, neither Party shall have the right to make an election under the Cooperative Research and Technology Enhancement Act of 2004, 35 U.S.C. 103 (c)(2)-(c)(3) when exercising its rights under this Article 8 without the prior written consent of the other Party. With respect to any such permitted election, the Parties shall use reasonable efforts to cooperate and coordinate their activities with respect to any submissions, filings or other activities in support thereof.

9.GOVERNMENT APPROVALS.

9.1. AstraZeneca’s and Xxxxxxxxx’x Obligations. Each of AstraZeneca and Xxxxxxxxx shall use its good faith efforts to eliminate any concern on the part of any court or Government Authority regarding the legality of the proposed transaction, including, if required by federal or state antitrust authorities, promptly taking all steps to secure government antitrust clearance, including cooperating in good faith with any government investigation including the prompt production of documents and information demanded by a second request for documents and of witnesses if requested.

9.2. Additional Approvals. AstraZeneca and Xxxxxxxxx shall cooperate and use respectively all reasonable efforts to make all other registrations, filings and applications, to give all notices and to obtain as soon as practicable all governmental or other consents, transfers, approvals, orders, qualifications authorizations, permits and waivers, if any, and to do all other things necessary or desirable for the consummation of the transactions as contemplated hereby. Neither Party shall be required, however, to divest or out-license products or assets or materially change its business if doing so is a condition of obtaining

approval of the transactions contemplated by this Agreement.

9.3. Termination. If a report is required to be filed under any antitrust statute, either Party may, before the Effective Date, terminate this Agreement by written notice to the other Party, if, within [**] after the report is filed, approval of the transactions contemplated by this Agreement under such antitrust statute has not been obtained or the notice and waiting period, as may be extended, under such antitrust statute has not expired without adverse action regarding this Agreement or the transactions contemplated hereby. If this Agreement is terminated pursuant to this Section 9.3, then, notwithstanding any provision in this Agreement to the contrary, neither Party shall have any further obligation to the other Party with respect to the subject matter of this Agreement except for the obligations set forth in Section 6.1, which obligations shall survive any termination of this Agreement; provided that each Party shall within ten (10) days of such termination promptly refund to the other Party in full all amounts paid by such Party to the other Party in connection with this Agreement.

10.TERM AND TERMINATION.

10.1.Term. The term of this Agreement shall commence on the Effective Date and, unless earlier terminated as provided in this Section 10 shall continue in full force and effect on a country-by-country basis as long as any Collaboration Product is being Developed or Commercialized for use in the Field in the Territory (the “Term”)

10.2.Termination for Convenience; Termination by Mutual Agreement. AstraZeneca may terminate this Agreement in its entirety for any reason or no reason upon providing one hundred eighty (180) days’ prior written notice to Xxxxxxxxx. Additionally, the Parties may terminate this Agreement by mutual written agreement.

10.3.Termination for Cause.

10.3.1.Termination for Material Breach. In the event that a Party commits a material breach of its obligations under this Agreement that is not cured within sixty (60) days (or such other time period as mutually agreed by the Parties) after such Party receives written notice from the non-breaching Party, which notice shall specify the nature of the breach and demand its cure, the non-breaching Party may terminate this Agreement upon written notice to the breaching Party; provided, however, that a breach of this Agreement by AstraZeneca that relates solely to a country that is not a Major Market Country shall give Xxxxxxxxx a termination right only as to such country (any such termination, a “Country-Specific Termination”). Notwithstanding the foregoing, if either Party is alleged to be in material breach and disputes such termination through the dispute resolution procedures set forth in this Agreement, then the other Party’s right to terminate this Agreement shall be suspended for so long as such dispute resolution procedures are being pursued by the allegedly breaching Party in good faith and, if it is finally and conclusively determined that the allegedly breaching Party is in material breach, then the breaching Party shall have the right to cure such material breach after such determination within the cure period provided above in this Section 10.3.1.

10.3.2.Termination for Bankruptcy. This Agreement may be terminated by

written notice by either Party at any time during the term of this Agreement if the other Party shall file in any court or Agency, pursuant to any statute or regulation of any state or country, 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, or if the other Party proposes a written agreement of composition or extension of its debts, or if the other Party shall be served with an involuntary petition against it, filed in any insolvency proceeding, and such petition shall not be dismissed within sixty (60) days after the filing thereof, or if the other Party shall propose or be a Party to any dissolution or liquidation, or if the other Party shall make an assignment for the benefit of its creditors.

10.4.Effect of Termination.

10.4.1.Effects of Termination for Convenience. If this Agreement is terminated for convenience pursuant to Section 10.2, the following provisions shall apply:

(a)Nothing in this Agreement shall be construed as prohibiting Xxxxxxxxx from Developing, Manufacturing and Commercializing a Collaboration Compound and the Collaboration Product in the Field in the Territory;

(b)All licenses granted by Xxxxxxxxx to AstraZeneca hereunder shall automatically terminate;

(c)AstraZeneca shall, and hereby does, assign to Xxxxxxxxx all right, title and interest in and to: (i) all Regulatory Submissions and Regulatory Approvals Controlled by AstraZeneca or any Affiliate pertaining to Collaboration Compounds, Collaboration Products and Diagnostic Products in the Field in the Territory and (ii) all of AstraZeneca’s interest in any copyrights to the extent necessary or useful for Commercializing the Collaboration Product;

(d)If, at the time AstraZeneca terminates the Agreement, a Collaboration Product is then being sold using an AstraZeneca-owned Trademark, AstraZeneca shall, assign all of AstraZeneca’s interest in any Trademark (including the goodwill symbolized by such Trademark), on commercially reasonable terms to be mutually agreed upon by the Parties;

(e)AstraZeneca shall grant, and shall be deemed to grant, to Xxxxxxxxx and its Sublicensees a Right of Reference to all data generated in any Clinical Trials undertaken by AstraZeneca , its Affiliates or Sublicensees in accordance with this Agreement (including all such Regulatory Submissions, Regulatory Approvals and Clinical Trial data related to any Diagnostic Product and any Combination Collaboration Products in which the other active ingredients are non-proprietary), and AstraZeneca shall provide a signed statement to this effect, if requested by Xxxxxxxxx , in accordance with 21 C.F.R. § 314.50(g)(3) (or any analogous Applicable Law recognized outside of the United States);

(f)AstraZeneca shall, and hereby does, grant to Xxxxxxxxx a perpetual, royalty-free, irrevocable, non-exclusive license in the Territory to use the data generated in Clinical Trials undertaken by AstraZeneca , its Affiliates or

Sublicensees hereunder (including all such Regulatory Submissions, Regulatory Approvals and Clinical Trial data related to any Combination Collaboration Products ) for the Development and Commercialization of Collaboration Compounds, Collaboration Products and Diagnostic Products in the Field in the Territory;

(g)All licenses granted to Xxxxxxxxx hereunder shall continue, and AstraZeneca shall, and hereby does, grant to Xxxxxxxxx an exclusive (even as to AstraZeneca) license in the Territory (with the right to sublicense on terms consistent with Section 2.5) (i) to practice any invention claimed in the AstraZeneca Patent Rights or Joint Patent Rights, (ii) to practice the AstraZeneca Know-How and Joint Know-How and (iii) to practice any other Patent Right or Know Controlled by AstraZeneca on the effective date of termination that arose before the effective date of termination and was either in use by AstraZeneca or was actively being considered for use in connection with the Development, Manufacture or Commercialization of any Collaboration Compound, Collaboration Product or Diagnostic Product, in each case ((i) – (iii)), solely to the extent necessary to Develop, Manufacture and Commercialize a Collaboration Compound, Collaboration Product or Diagnostic Product, as applicable, in the Field in the Territory;

(h)Notwithstanding anything in Section 3.3.2(a) to the contrary, AstraZeneca shall reasonably cooperate with Xxxxxxxxx to assure a smooth transition, at Xxxxxxxxx’x expense, of any Clinical Trials in progress related to a Collaboration Compound or Collaboration Product in the Field, which Xxxxxxxxx determines to continue in compliance with Applicable Laws and ethical guidelines applicable to the transfer or termination of any such Clinical Trials. In the event that Xxxxxxxxx informs AstraZeneca that it does not intend to continue specific Development activities then in progress, costs incurred in closing out such activities shall be borne by AstraZeneca;

(i)Until termination is effective, each Party shall continue to perform its obligations under the Development Plan (if still in effect) and shall pay all costs allocated to it in accordance with this Agreement, including the Development Budget (if still in effect), except with respect to activities that Xxxxxxxxx elects to discontinue and subject to Section 5.7.2(e) and 5.7.2(f);

(j)At Xxxxxxxxx’x request, Xxxxxxxxx may purchase, [**], all of the inventory of bulk or finished Collaboration Products held by AstraZeneca as of the date of termination (including raw materials, intermediates and finished, unfinished, or partially finished goods). Xxxxxxxxx shall notify AstraZeneca within ten (10) days after the date of termination whether Xxxxxxxxx wishes to purchase such inventory. In the event Xxxxxxxxx does not purchase such inventory, then AstraZeneca and its Affiliates shall be permitted to sell such inventory, provided that such sales occur within six (6) months after termination, and provided further that AstraZeneca shall remain obligated to pay, and report to Xxxxxxxxx on, Net Sales of such inventory; and

(k)At Xxxxxxxxx’x request, AstraZeneca shall use Commercially Reasonable Efforts to assign to Xxxxxxxxx to the extent assignment is permitted by such agreements and provided that AstraZeneca is not required to pay any consideration or commence litigation in order to effect an assignment of any such agreement any Third Party agreements then in effect for the Manufacture of Collaboration Compound or Collaboration Product.

10.4.2.Effects of Termination for Material Breach.

(a)If this Agreement is terminated by Xxxxxxxxx pursuant to Section 6.4.3 or 10.3, all licenses granted by Xxxxxxxxx to AstraZeneca shall automatically terminate. Without limiting the foregoing, in the event this Agreement is terminated by Xxxxxxxxx for a material breach of AstraZeneca pursuant to Section 6.4.3 or 10.3.1 , the effects of termination set forth in Section 10.4.1 shall apply; provided, however, that in the event of a Country-Specific Termination pursuant to Section 10.3.1, such effects of termination shall apply only with respect to the applicable country.

(b)In the event that AstraZeneca has the right to terminate this Agreement pursuant to Section 10.3.1, AstraZeneca may elect to either (x) terminate this Agreement in its entirety pursuant to Section 10.3.1 or (y) elect, as its sole and exclusive remedy with respect to such breach, to forego its right to terminate this Agreement pursuant to Section 10.3.1, in which case the provisions of clauses (i) – (iii) below shall apply.

(i)AstraZeneca’ s sole and exclusive remedy with respect to such breach shall be to offset from amounts due under Sections 5.2 and 5.3 the amount of any agreed-upon or proven damages (“Damages”).

(ii)Pending any agreement between the Parties on the amount of the Damages or a final, non-appealable judgment in a court of competent jurisdiction as to the amount of the Damages (“Final Resolution”), AstraZeneca shall set up an escrow account into which it shall pay, as they become due, all milestones and royalty payments owed to Xxxxxxxxx under Section 5.2 or 5.3.

(iii)Upon Final Resolution, any Damages owed to AstraZeneca in respect of the applicable breach shall be deducted by AstraZeneca from amounts paid into such escrow account. In the event the amounts contained in such escrow account exceed the Damages, the amounts remaining in such escrow account shall be released to Xxxxxxxxx no later than five (5) Business Days after Final Resolution. In the event the amounts contained in such escrow account are insufficient to cover the Damages, the balance of any such

amounts may be deducted from the next applicable payment owed by AstraZeneca to Xxxxxxxxx under Section 5.2 or 5.3 and may be carried forward until fully exhausted.

10.5.Rights in Bankruptcy. All rights and licenses granted under or pursuant to this Agreement by Xxxxxxxxx and AstraZeneca are, and shall otherwise be deemed to be, for purposes of Section 365(n) of the United States Bankruptcy Code, licenses of rights to “intellectual property” as defined under Section 101 of the United States Bankruptcy Code. The Parties agree that each Party, as licensee of certain rights under this Agreement, shall retain and may fully exercise all of its rights and elections under the United States Bankruptcy Code. The Parties further agree that, in the event of the commencement of a bankruptcy proceeding by or against a Party under the United States Bankruptcy Code, the other Party shall be entitled to a complete duplicate of (or complete access to, as appropriate) any intellectual property licensed to such other Party and all embodiments of such intellectual property, which, if not already in such other Party’s possession, shall be promptly delivered to it (a) upon any such commencement of a bankruptcy proceeding upon such other Party’s written request therefor, unless the bankrupt Party elects to continue to perform all of its obligations under this Agreement or (b) if not delivered under clause (a), following the rejection of this Agreement by the bankrupt Party upon written request therefor by the other Party.

10.6.Survival of Certain Obligations. Expiration or termination of this Agreement shall not relieve the Parties of any obligation accruing before such expiration or termination. The provisions of this Agreement that must, by their nature, survive expiration or termination of this Agreement to give effect to their intent, shall so survive, including Sections 2.4, 2.6, 6, 9 and 11 Any expiration or early termination of this Agreement shall be without prejudice to the rights of either Party against the other accrued or accruing under this Agreement before termination.

11.PRODUCT LIABILITY, INDEMNIFICATION AND INSURANCE.

11.1.Indemnification by Xxxxxxxxx. Xxxxxxxxx shall indemnify, defend and hold harmless AstraZeneca, its Affiliates, and each of its and their respective employees, officers, directors, agents and Sublicensees (each, a “AstraZeneca Indemnified Party”) from and against any and all losses, damages, liabilities, settlements, penalties, fines and expenses (including reasonable attorneys’ fees and expenses) (collectively, “Liability”) that the AstraZeneca Indemnified Party may be required to pay to one or more Third Parties to the extent resulting from or arising out of:

(a)any Xxxxxxxxx representation or warranty set forth herein being untrue in any material respect when made or any material breach by Xxxxxxxxx of any of its covenants or obligations hereunder; or

(b)the gross negligence or willful misconduct by or of Xxxxxxxxx, its Affiliates and their respective officers, directors, agents and Sublicensees in performing any of their obligations under this Agreement; or

(c)Xxxxxxxxx’x or its Affiliates’ Development of a Collaboration Compound; except in each case, to the extent caused by the gross negligence or willful misconduct of AstraZeneca or any AstraZeneca Indemnified Party, or by breach of this Agreement by AstraZeneca.

11.2.Indemnification by AstraZeneca. AstraZeneca shall indemnify, defend and hold harmless Xxxxxxxxx, its Affiliates, and each of its and their respective employees, officers, directors, agents and Sublicensees (each, a “Xxxxxxxxx Indemnified Party”) from and against any and all Liabilities that the Xxxxxxxxx Indemnified Party may be required to pay to one or more Third Parties to the extent resulting from or arising out of:

(a)any AstraZeneca representation or warranty set forth herein being untrue in any material respect when made or a material breach by AstraZeneca of any of its covenants or obligations hereunder; or

(b)the gross negligence or willful misconduct by or of AstraZeneca, its Affiliates and their respective officers, directors, agents and Sublicensees in performing any of their obligations under this Agreement; or

(c)AstraZeneca’s Development, Manufacture or Commercialization of a Collaboration Compound or Collaboration Product; except in each case, to the extent caused by the gross negligence or willful misconduct of Xxxxxxxxx or any Xxxxxxxxx Indemnified Party, or by breach of this Agreement by Xxxxxxxxx.

11.3.Procedure. Each Party shall notify the other in the event it becomes aware of a claim for which indemnification may be sought hereunder or for which Liability is shared pursuant to this Section 11. In case any proceeding (including any governmental investigation) shall be instituted involving any Party in respect of which indemnity may be sought pursuant to this Section 11, such Party (the “Indemnified Party”) shall provide the other Party (the “Indemnifying Party”) with prompt written notice of such proceeding (the “Indemnification Claim Notice”). Promptly after the Indemnifying Party receives the Indemnification Claim Notice, the Indemnifying Party and Indemnified Party shall meet to discuss how to respond to any claims that are the subject matter of such proceeding. At its option, the Indemnifying Party may assume the defense of any Third Party claim subject to indemnification as provided for in this Section 11.3 by giving written notice to the Indemnified Party within thirty (30) days (or until such time provided in any applicable extension to appropriately answer any complaint, if any, but no longer than seventy (70) days, provided that the Indemnified Party makes all reasonable efforts to obtain any such extension) after the Indemnifying Party’s receipt of an Indemnification Claim Notice, provided that (a) the claim solely seeks monetary damages and (b) the Indemnifying Party expressly agrees in writing that as between the Indemnifying Party and the Indemnified Party, the Indemnifying Party shall be solely obligated to satisfy and discharge the claim in full (the matters described in (a) and (b), the “Litigation Conditions”). The Indemnifying Party may, at any time, assume all such defense if the Litigation Conditions are not satisfied

at any time. Upon assuming the defense of a Third Party claim in accordance with this Section 11.3, the Indemnifying Party shall be entitled to appoint lead counsel in the defense of the Third Party claim. Should the Indemnifying Party assume and continue the defense of a Third Party claim, except as otherwise set forth in this Section 11.3, the Indemnifying Party will not be liable to the Indemnified Party for any legal expenses subsequently incurred by such Indemnified Party in connection with the analysis, defense or settlement of the Third Party claim. Without limiting this Section 11.3, any Indemnified Party will be entitled to participate in, but not control, the defense of a Third Party claim for which it has sought indemnification hereunder and to employ counsel of its choice for such purpose; provided, however, that such employment will be at the Indemnified Party’s own expense unless (i) the employment thereof has been specifically authorized by the Indemnifying Party in writing, (ii) the Indemnifying Party has failed to assume and actively further the defense and employ counsel in accordance with this Section 11.3 (in which case the Indemnified Party will control the defense) or (iii) the Indemnifying Party no longer satisfies the Litigation Conditions. With respect to any Liability relating solely to the payment of money damages in connection with a Third Party claim that will not result in the Indemnified Party’s becoming subject to injunctive or other relief or otherwise adversely affect the business of the Indemnified Party in any manner, and as to which the Indemnifying Party will have acknowledged in writing the obligation to indemnify the Indemnified Party hereunder, and subject to the Litigation Conditions being satisfied, the Indemnifying Party will have the sole right to consent to the entry of any judgment, enter into any settlement or otherwise dispose of such Liability, on such terms as the Indemnifying Party, in its reasonable discretion, will deem appropriate (provided that such terms shall include a complete and unconditional release of the Indemnified Party from all liability with respect thereto), and will transfer to the Indemnified Party all amounts which said Indemnified Party will be liable to pay prior to the time of the entry of judgment. With respect to all other Liabilities in connection with Third Party claims, where the Indemnifying Party has assumed the defense of the Third Party claim in accordance with this Section 11.3, the Indemnifying Party will have authority to consent to the entry of any judgment, enter into any settlement or otherwise dispose of such Liability provided that it obtains the prior written consent of the Indemnified Party (which consent will be at the Indemnified Party’s reasonable discretion). The Indemnifying Party that has assumed the defense of the Third Party claim in accordance with this Section 11.3 will not be liable for any settlement or other disposition of a Liability by an Indemnified Party (but in no event to include any court judgment or judicial or administrative order or disposition) that is reached without the written consent of such Indemnifying Party. No Indemnified Party will admit any liability with respect to, or settle, compromise or discharge, any Third Party claim without first offering to the Indemnifying Party the opportunity to assume the defense of the Third Party claim in accordance with this Section 11.3. If the Indemnifying Party chooses to defend or prosecute any Third Party claim, the Indemnified Party will cooperate in the defense or prosecution thereof and will furnish such records, information and testimony, provide such witnesses and attend such conferences, discovery proceedings, hearings, trials and appeals as may be reasonably requested in connection with such Third Party claim. Such cooperation will include access during normal business hours afforded to the Indemnifying Party to, and reasonable retention by the Indemnified Party of, records and information that are reasonably relevant to such Third Party claim, and making employees and agents available on a mutually convenient basis to provide additional

information and explanation of any material provided hereunder, and the Indemnifying Party will reimburse the Indemnified Party for all its reasonable out-of-pocket expenses incurred in connection with such cooperation.

00.0.Xxxxxxxxx. The Parties shall maintain insurance with creditworthy insurance companies or self insure in accordance with Applicable Law against such risks and in such amounts as are usually maintained or insured against by other companies of established repute engaged in the same or a similar business.

00.0.Xxx. AstraZeneca shall indemnify, defend and hold harmless Xxxxxxxxx, and its Affiliates, from and against any and all Liabilities that Xxxxxxxxx or its Affiliates are required to pay in respect of non-recoverable Indirect Taxes or corporation taxes arising on assessment solely as a consequence of the alteration of the mechanics of settlement between the Parties under Section 5.3.1 and 5.3.2 (an “Indemnifying Tax Payment”). To the extent that AstraZeneca makes an Indemnifying Tax Payment to Xxxxxxxxx pursuant to this Section 11.5 and, subsequently, Xxxxxxxxx receives a reimbursement of such tax liabilities for which an Indemnifying Tax Payment was made, to the extent that Xxxxxxxxx by making such payment would not be worse off compared to the situation where no additional tax had been required to be paid, Xxxxxxxxx shall either: (i) pay to AstraZeneca the full amount of such tax refund or relief; or (ii) issue a credit note of an equivalent amount to such credit, refund or relief against future invoices due to Xxxxxxxxx. Furthermore, Xxxxxxxxx shall use Commercially Reasonable Efforts to appeal any and all assessments raised by a tax authority which may result in an Indemnifying Tax Payment being made and will notify AstraZeneca of any such assessment within 14 days of receipt.

11.6.Liability Limitations.

00.0.0.Xx Consequential Damages. EXCEPT WITH RESPECT TO ANY BREACH OF SECTION 6.1 (CONFIDENTIALITY), IN NO EVENT WILL EITHER PARTY BE LIABLE TO THE OTHER FOR ANY CONSEQUENTIAL, INCIDENTAL, INDIRECT, SPECIAL, PUNITIVE OR EXEMPLARY DAMAGES UNDER THIS AGREEMENT, EXCEPT TO THE EXTENT THE DAMAGES RESULT FROM A PARTY’S FRAUD OR WILLFUL MISCONDUCT OR ARE PAYABLE IN CONNECTION WITH A PARTY’S INDEMNIFICATION OBLIGATIONS UNDER THIS SECTION 11 FOR LIABILITY OWED TO THIRD PARTIES.

11.6.2.Scope of Xxxxxxxxx’x Liability. In no event shall Xxxxxxxxx’x Liability under this Agreement exceed, [**] (the “Liability Cap”); provided, however, that such Liability Cap shall not apply to any Liability based on or arising out of any death or personal injury to a Third Party resulting from any negligence of Xxxxxxxxx, its Affiliates or Sublicensees.

12.MISCELLANEOUS.

12.1.Governing Law, Jurisdiction; Dispute Resolution.

12.1.1.Governing Law. The interpretation and construction of this Agreement

shall be governed by the laws of England, and the Parties hereby submit to the non-exclusive jurisdiction of the English courts.

12.1.2.Dispute Resolution. In the event of a dispute arising out of or relating to this Agreement either Party shall provide written notice of the dispute to the other, in which event the dispute shall be referred to the executive officers designated below or their successors, for attempted resolution by good faith negotiations within [**] after such notice is received. Said designated officers are initially as follows:

For Xxxxxxxxx:	Chief Executive Officer, Xxxxxxxxx MediPharma Limited
For AstraZeneca:	its Executive Vice President, Innovative Medicines or his
	designee

In the event the designated executive officers do not resolve such dispute within the allotted [**], either Party may, after the expiration of the [**] period, seek to resolve the dispute through reference to the courts in accordance with Section 12.1.1. Notwithstanding the preceding, the Parties acknowledge that the failure of the Parties to reach consensus as to any matter, which failure does not involve a breach by a Party of its obligations hereunder, shall not be deemed a dispute which may be referred for resolution by the Parties under this Section 12.1.2.

12.1.3.Agent for Service.

(a)To the extent that any injunctive or other Proceedings (as defined below) are sought in the court of England, the Parties hereby irrevocably agrees that any Service Document (as defined below) may be sufficiently and effectively served on it in connection with Proceedings by service on its agent, provided that if a replacement agent has been appointed and notified to the other party pursuant to Section 12.1.3(d), then by service on such replacement agent.

(b)Any Service Document served pursuant to Section 12.1.3(a) shall be marked for the attention of:

If to Xxxxxxxxx:


Address:		c/x Xxxxxxxxx Whampoa Agents (UK) Limited
		Xxxxxxxxx House
		5 Xxxxxx Road
		Battersea
		Xxxxxx XX0 1 4AN
		United Kingdom
Fax no:		x00 00 0000 0000
Attention:		The Company Secretary

If to AstraZeneca:


Address:		1 Xxxxxxx Xxxxx Avenue
		Xxxxxxxxx Xxxxxxxxxx Xxxxxx Xxxxxxxxx, XX XX0 0XX
Fax no:		x00 00 0000 0000
Attention:		The Company Secretary

(c)Any Service Document addressed in accordance with Section 12.1.3(b) shall be deemed to have been duly served if: (i) left at the specified address at the time it is left; (ii) sent by first class post, two working days after the day of posting; or (iii) sent by facsimile transmission, when the electronic acknowledgment is received by the sender.

(d)If either the agent of the Parties referred to in Section 12.1.3(b) (or any replacement agent appointed pursuant to this sub-section) at any time ceases for any reason to act as such, the Parties (as the case may be) shall appoint a replacement agent to accept service having an address for service in the United Kingdom and shall notify the other party of the name and address of the replacement agent.

(e)In this Section 12.1.3: (i) “Proceedings” means any proceeding, action arising out of or in connection with this Agreement, as contemplated by Clause 12.1.3(a); and (ii) “Service Document” means a writ, summons, order, judgment or other process issued out of the courts of England in connection with any Proceedings.

(f)A person who is not a party to this Agreement shall have no rights under the Contracts (Rights of Third Parties) Xxx 0000 to enforce any of its terms.

12.2.Force Majeure. No liability shall result from, and no right to terminate shall arise, in whole or in part, based upon any delay in performance or non-performance, in whole or in part, by either of the Parties to this Agreement to the extent that such delay or non-performance is caused by an event of Force Majeure. “Force Majeure” means an event that is beyond a non-performing Party’s reasonable control, including an act of God, act of the other Party, strike, lock-out or other industrial/labor dispute not involving the non-performing Party’s own employees, war, riot, civil commotion, terrorist act, malicious damage, epidemic, quarantine, fire, flood, storm, natural disaster or compliance with any law or governmental order, rule, regulation or direction, whether or not it is later held to be invalid or inapplicable. The Force Majeure Party shall within ten (10) days of the occurrence of the Force Majeure event, give written notice to the other Party stating the nature of the Force Majeure event, its anticipated duration and any action being taken to avoid or minimize its effect. Any suspension of performance shall be of no greater scope and of no longer duration than is reasonably required and the Force Majeure Party shall use reasonable effort to remedy its inability to perform; provided, however, if the suspension of performance continues or is anticipated to continue for thirty (30) days after the date of the occurrence, the unaffected Party shall have the right but not the obligation to perform on behalf of the Force Majeure Party for a period of such Force Majeure and such additional period as may be

reasonably required to assure a smooth and uninterrupted transition of such activities. If such failure to perform would constitute a material breach of this Agreement in the absence of such event of Force Majeure, and continues for six (6) months from the date of the occurrence and the Parties are not able to agree on appropriate amendments within such period, such other Party shall have the right, notwithstanding the first sentence of this Section 12.3, to terminate this Agreement immediately by written notice to the Force Majeure Party, in which case neither Party shall have any liability to the other except for those rights and liabilities that accrued prior to the date of termination.

12.3.Waiver and Non-Exclusion of Remedies. A Party’s failure to enforce, at any time or for any period of time, any provision of this Agreement, or to exercise any right or remedy shall not constitute a waiver of that provision, right or remedy or prevent such Party from enforcing any or all provisions of this Agreement and exercising any rights or remedies. To be effective any waiver must be in writing. The rights and remedies provided herein are cumulative and do not exclude any other right or remedy provided by law or otherwise available except as expressly set forth herein.

12.4.Notices.

12.4.1.Notice Requirements. Any notice, request, demand, waiver, consent, approval or other communication permitted or required under this Agreement shall be in writing, shall refer specifically to this Agreement and shall be deemed given only if delivered by hand or sent by facsimile transmission (with transmission confirmed) or by internationally recognized overnight delivery service that maintains records of delivery, addressed to the Parties at their respective addresses specified in Section 12.4.2 or to such other address as the Party to whom notice is to be given may have provided to the other Party in accordance with this Section 12.4.1. Such Notice shall be deemed to have been given as of the date delivered by hand or transmitted by facsimile (with transmission confirmed) or on the second business day (at the place of delivery) after deposit with an internationally recognized overnight delivery service. This Section is not intended to govern the day-to-day business communications necessary between the Parties in performing their obligations under the terms of this Agreement.

12.4.2.Address for Notice.


	Xxxxxxxxx:

		Xxxxxxxxx MediPharma Limited
		Xxxxxxxx 0, 000 Xxxxxx Xxxx
		Zhangjiang High Tech Park
		Xxxxxxxx, Xxxxx 000000
		Attn: Chief Executive Officer, Xxxxxxxxx MediPharma Limited Fax: 00-00-00000000

	With a copy to:

		XX Xxxxxxxxx Holdings Limited 48/F Xxxxxx Kong Center
		2 Queen’s Road


		Central
		Hong Kong
		Attn: Head Group General Counsel & Company Secretary Fax: x000 0000 0000

	AstraZeneca:
		AstraZeneca AB
		X-000 00 Xxxxxxxxxx
		Sweden
		Attn: The Company Secretary Fax: x00 0 000 000 00

	With a copy to:

		AstraZeneca UK Limited
		Eastbrook House Shaftesbury Road Cambridge
		XX0 0XX
		United Kingdom
		Attn: Senior VP, Business Development Operations

12.5.Entire Agreement. As of the Restatement Date, the Original Agreement is hereby amended, supplemented, modified and restated in its entirety as described herein, and this Agreement shall hereby constitute the entire agreement between the Parties with respect to the subject matter of the Agreement. This Agreement supersedes all prior agreements, whether written or oral, with respect to the subject matter hereof. Each Party confirms that it is not relying on any representations, warranties or covenants of the other Party except as specifically set out in this Agreement. Nothing in this Agreement is intended to limit or exclude any liability for fraud. All Schedules or Exhibits referred to in this Agreement are intended to be and are hereby specifically incorporated into and made a part of this Agreement. In the event of any inconsistency between any such Schedules or Exhibits and this Agreement, the terms of this Agreement shall govern.

12.6.Amendment. Any amendment or modification of this Agreement must be in writing and signed by authorized representatives of both Parties.

12.7.Assignment. Neither Party may assign its rights or delegate its obligations under this Agreement, in whole or in part without the prior written consent of the other Party, except that each Party shall always have the right, without such consent, (a) to perform any or all of its obligations and exercise any or all of its rights under this Agreement through any of its Affiliates and, (b) on written notice to the other Party, assign any or all of its rights and delegate or subcontract any or all of its obligations hereunder to (i) any of its Affiliates, (ii) a successor of all or substantially all of the business of such Party, whether by way of merger, sale of stock, sale of assets or other transaction (or series of transactions) or (iii) a successor of that portion of a Party’s business to which this Agreement pertains. Any

permitted successor or assignee of rights or obligations hereunder shall, in a writing to the other Party, expressly assume performance of such rights or obligations. Notwithstanding the foregoing, each Party shall remain responsible for any failure to perform on the part of any such Affiliates. Any attempted assignment or delegation in violation of this Section shall be void.

00.0.Xx Benefit to Others. The provisions of this Agreement are for the sole benefit of the Parties and their successors and permitted assigns, and they shall not be construed as conferring any rights in any other persons except as otherwise expressly provided in this Agreement.

12.9.Counterparts. This Agreement may be executed in any number of counterparts, each of which shall be deemed an original and all of which taken together shall be deemed to constitute one and the same instrument. An executed signature page of this Agreement delivered by facsimile transmission shall be as effective as an original executed signature page.

12.10.Severability. To the fullest extent permitted by applicable law, the Parties waive any provision of law that would render any provision in this Agreement invalid, illegal or unenforceable in any respect. If any provision of this Agreement is held to be invalid, illegal or unenforceable, in any respect, then such provision will be given no effect by the Parties and shall not form part of this Agreement. To the fullest extent permitted by applicable law and if the rights or obligations of any Party will not be materially and adversely affected, all other provisions of this Agreement shall remain in full force and effect and the Parties will use their best efforts to negotiate a provision in replacement of the provision held invalid, illegal or unenforceable that is consistent with applicable law and achieves, as nearly as possible, the original intention of the Parties.

12.11.Further Assurance. Each Party shall perform all further acts and things and execute and deliver such further documents as may be reasonably necessary or as the other Party may reasonably require to implement or give effect to this Agreement.

12.12.Publicity. The Parties may jointly or separately issue press releases, public announcements, or other public disclosures regarding the Agreement or its subject matter or any amendment, provided that (i) at the minimum 15 days ahead of the issuance of a potential press release or other public disclosure, the Party wishing to issue such press release or other disclosure consults with the other Party reasonably and in good faith with respect to the text and timing of any such press releases or other public disclosure relating to the Agreement or its subject matter including any amendments thereto and (ii) the other Party has given its consent to such release, such consent not be unreasonably withheld. Notwithstanding the foregoing, either Party may issue such press releases or other public disclosure as it determines provided that such release is, based on the advice of counsel, and is reasonably necessary to comply with the applicable laws or regulations or for appropriate market disclosure in such country or which are consistent with information disclosed in prior releases properly made hereunder provided that such information remains accurate as of such time and provided the frequency and form of such disclosure are reasonable.

12.13.Relationship of the Parties. The status of a Party under this Agreement shall be that of an independent contractor. Nothing contained in this Agreement shall be construed as creating a partnership, joint venture, or agency relationship between the Parties or, except as otherwise expressly provided in this Agreement, as granting either Party the authority to bind or contract any obligation in the name of or on the account of the other Party or to make any statements, representations, warranties, or commitments on behalf of the other Party. All Persons employed by a Party or any of its Affiliates shall be employees of such Party or its Affiliates and not of the other Party or such other Party’s Affiliates and all costs and obligations incurred by reason of any such employment shall be for the account and expense of such Party or its Affiliates, as applicable.

12.14.Subcontracting. Xxxxxxxxx may, in its sole discretion, use one or more Affiliates or Third Party contractors to perform any or all of its obligations under this Agreement, provided that Xxxxxxxxx shall remain responsible for its obligations under the Agreement and shall be responsible for the performance of each such Affiliate and Third Party subcontractor.

12.15.English Language. This Agreement is written and executed in the English language. Any translation into any other language shall not be an official version of this Agreement and in the event of any conflict in interpretation between the English version and such translation, the English version shall prevail. English shall be the official language of this Agreement and all communications between the Parties shall be conducted in that language.

00.00.Xxxxxxxxxxxx. Except where the context requires otherwise, whenever used the singular includes the plural, the plural includes the singular, the use of any gender is applicable to all genders and the word “or” has the inclusive meaning represented by the phrase “and/or”. Whenever this Agreement refers to a number of days, unless otherwise specified, such number refers to calendar days. The headings of this Agreement and any descriptions of Schedules and Exhibits or descriptions of cross references are for convenience of reference only and do not define, describe, extend or limit the scope or intent of this Agreement or the scope or intent of any provision contained in this Agreement. The terms “including,” “include(s),” “such as,” and “for example” as used in this Agreement mean including the generality of any description preceding such term and shall be deemed to be followed by “without limitation.”

IN WITNESS WIIERFOF. duly authorized representatives of the Parties have duly executed this Agreement to be effective as of the Restatement Date.


ASTRAZENECA AB (publ)		和记黄埔医药（上海）有限公司
By	/s/[**]	By	/s/[**]
Name:	[**]	Name:	[**]
Title:	Authorised signatory	Title:	Director

[SIGNATURE PAGE TO LICENSE AND COLLABORATION AGREEMENT]

Schedule 1.11

Back-Up Compounds


XXXXXXXXX COMPOUND CODE	EXAMPLE NUMBER*	CHEMICAL NAME
[**]	[**]	[**]
[**]	[**]	[**]

[**].

Schedule 1.19

Collaboration Compound



XXXXXXXXX COMPOUND CODE	HMPL-504
GENERIC NAME	Volitinib
CHEMICAL NAME	[**]
EXAMPLE NUMBER*	[**]

[**].

Schedule 1.33

Development Plan and Development Budget

[**]

Schedule 1.49

Xxxxxxxxx Patent Rights

The following are the pending patent applications related to the Collaboration Compound and the Back-Up Compounds.


	COUN -	APPLICATION /	FILING	STATUS	TITLE
	TRY	PUBLICATION NO.	DATE
1	[**]	[**]	[**]	[**]	[**]
	[**]	[**]	[**]	[**]	[**]
	[**]	[**]	[**]	[**]	[**]
2	[**]	[**]	[**]	[**]	[**]
	[**]	[**]	[**]	[**]	[**]

Schedule 4.1.6

China Life Cycle Indications

(1)SACHI Study – a China Phase III registration study of savolitinib plus osimertinib in 1st, 2nd and 3rd generation EGFR inhibitor refractory, MET amplified NSCLC patients;

(2)Gastric Cancer Study – a China Phase II study, with registration intent, of savolitinib (either as monotherapy or in combination with durvalumab) in second-line or above gastric cancer; and

(3)China Basket Study – an exploratory study in approximately 20-30 patients (details of which to be defined and agreed in writing by the Parties) in tumors with driver MET genetic alterations.

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