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Collaboration and License Agreement

 

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Title:

Collaboration and License Agreement

Entities:

Array BioPharma Inc.; AstraZeneca AB; Astrazeneca UK Ltd.

Date:

2004

Size:

Preview shows 18KB of 169KB total

Price:

$68

ID:

#306890

 

 

► Licensing ► Licenses ► Collaboration & License Agreements
► Biotechnology & Drugs
► Biotech & Drugs ► Medical Laboratories

 

 

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[ * ] = Certain confidential information contained in this document, marked by brackets, has been omitted and filed separately with the Securities and Exchange Commission pursuant to Rule 24b-2 of the Securities Exchange Act of 1934, as amended.

 

COLLABORATION AND LICENSE AGREEMENT

 

THIS COLLABORATION AND LICENSE AGREEMENT (the Agreement) is made effective as of the 18th day of December, 2003 (Effective Date) by and between Array BioPharma Inc., a Delaware corporation of 3200 Walnut Street, Boulder, Colorado 80301  (Array), and AstraZeneca AB, a company incorporated in Sweden under no. 556011-7482 with offices at S-151 85 Sdertlje, Sweden  (AZ).  Array and AZ are each referred to herein by name or as a Party or, collectively, as Parties.

 

RECITALS

 

A.                                   Array owns certain intellectual property rights and know-how with respect to that certain chemical compound designated as ARRY-142886, and believes that ARRY-142886 has the potential to become an anti-cancer agent with significant worldwide sales.

 

B.                                     Array desires to collaborate with a pharmaceutical company with oncology research, development and commercialization expertise with the aim of developing and commercializing ARRY-142886 worldwide so as to realize its therapeutic and commercial potential.  AZ is a leader in the research and development of pharmaceutical compounds and possesses pharmaceutical research, development and commercialization capabilities, as well as proprietary compounds and technology in the field of cancer treatment.

 

C.                                     AZ desires to collaborate with Array in the development and commercialization of ARRY-142886 for the treatment of cancer.

 

D.                                    In addition, Array has an ongoing research program to identify and develop additional small molecule pharmaceutical products, the mechanism of action of which is the direct binding and inhibition of MEK, for the treatment of cancer, and has developed and continues to develop certain novel, proprietary compounds and technology in this field.  AZ is interested in collaborating with Array to develop the compounds identified by Array, and to develop and commercialize pharmaceutical products directed to MEK in the field of cancer treatment.

 

Now, therefore, in consideration of the premises and mutual covenants herein contained, and for other good and valuable consideration, the receipt and sufficiency of which are hereby acknowledged, the Parties hereto agree as follows:

 

ARTICLE I - DEFINITIONS

 

The following terms shall have the following meanings as used in this Agreement:

 



 

1.1                                 Abandoned Product shall have the meaning ascribed to it in Section 11.3.2.

 

1.2                                 Affiliate shall mean any corporation or other entity which is directly or indirectly controlling, controlled by or under common control with a Party hereto for so long as such control exists.  For the purposes of this Section 1.2, control shall mean the direct or indirect ownership of at least fifty percent (50%) of the outstanding shares or other voting rights of the subject entity having the power to vote on or direct affairs of the entity, or if not meeting the preceding, the maximum voting right that may be held by the particular Party under the laws of the country where such entity exists.

 

1.3                                 Array Existing Technology shall mean Array Patents and Array Know-How, in each case Controlled by Array as of the Effective Date, that are reasonably necessary or useful for the Parties to conduct their respective activities under the Research Program and the Process Program and for AZ to develop, make, have made, use, import, offer to sell and sell, research, register, formulate, have used, export, transport, distribute, promote, market or have sold or otherwise dispose or offer to dispose of Candidate Drugs or Licensed Products in the Field.

 

1.4                                 Array Know-How shall mean Information which (a) Array discloses to AZ under this Agreement or specifically in anticipation of this Agreement and (b) is within the Control of Array.  Notwithstanding anything herein to the contrary, Array Know-How excludes published Array Patents.

 

1.5                                 Array Patents shall mean the Patents set out in Exhibit 1.5.

 

1.6                                 AZ Existing Technology shall mean AZ Patents and AZ Know-How, in each case Controlled by AZ or its Affiliates as of the Effective Date, that are reasonably necessary for the discovery, development, manufacture, use or sale of Candidate Drugs or Licensed Products.

 

1.7                                 AZ Know-How shall mean Information which (a) AZ discloses to Array under this Agreement or specifically in anticipation of this Agreement and (b) is within the Control of AZ or its Affiliates.  Notwithstanding anything herein to the contrary, AZ Know-How excludes published AZ Patents.

 

1.8                                 AZ Patents shall mean all Patents in the Territory owned or Controlled by AZ or its Affiliates.

 

1.9                                 Calendar Quarter means each successive period of three (3) calendar months commencing on 1st January, 1st April, 1st July and 1st October.

 

1.10                           Calendar Year means each successive period of twelve (12) calendar months commencing on 1st January.

 

1.11                           Candidate Drug shall mean a Compound selected for clinical development in accordance with Section 2.5 below.

 

2



 

1.12                           Candidate Drug Target Profile shall mean (i) those criteria set forth in Exhibit 1.12, and/or (ii) such other criteria as are approved by the JRC and agreed in writing by the Parties.  No criteria shall be deemed part of the Candidate Drug Target Profile under (ii) unless such criteria are formally approved by the JRC and agreed in writing by the Parties, regardless of whether such criteria are used informally or discussed by the Parties in the course of the Research Program.

 


 

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