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MATERIAL TRANSFER AGREEMENT

License Agreement

MATERIAL TRANSFER AGREEMENT | Document Parties: DARA BIOSCIENCES, INC. | America Stem Cell, Inc You are currently viewing:
This License Agreement involves

DARA BIOSCIENCES, INC. | America Stem Cell, Inc

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Title: MATERIAL TRANSFER AGREEMENT
Date: 10/13/2009
Industry: Biotechnology and Drugs     Sector: Healthcare

MATERIAL TRANSFER AGREEMENT, Parties: dara biosciences  inc. , america stem cell  inc
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MATERIAL TRANSFER AGREEMENT

 

            This Material Transfer Agreement (the "Agreement") effective as of March 24, 2008 (the "Effective Date") is made by and between America Stem Cell, Inc., a California corporation located at 135 Chinquapin Avenue, Carlsbad, CA 92008 ("ASC" or "Recipient"), and Dara BioSciences, Inc. located at 8601 Six Forks Road, Suite 160, Raleigh, NC 27615 ("Dara BioSciences, Inc."). ASC and Dara BioSciences, Inc. are referred to herein as a "Party" and collectively as the "Parties."

1.         Materials .

(a)        Dara BioSciences, Inc. is willing to transfer to Recipient the materials specified on Appendix A hereto ("Materials"), for the sole purpose of conducting preclinical efficacy research to establish the efficacy of Dara BioSciences, Inc.'s compounds for ex-vivo treatment of cord blood derived stem cells relative to promoting their homing/engraftment (the "Purpose").

(b)        The Materials and their use, including but not limited to cell homing and engraftment, are proprietary to Dara BioSciences, Inc., and Recipient acknowledges that the Materials and their use shall remain the sole and exclusive property of Dara BioSciences, Inc. Recipient shall retain control of Materials and shall not sell, transfer, disclose, distribute or otherwise release Materials or any progeny, derivative or part thereof, to any third party other than as permitted herein.

2.         Research Program . Recipient may use the Materials to conduct preclinical efficacy research to establish the efficacy of Dara BioSciences, Inc.' compounds identified on Appendix A for ex-vivo treatment of cord blood derived stem cells relative to promoting their homing/engraftment as specified in greater detail in Appendix B (the "Research Program").

3.         Limitation of Use . The Materials will be used by ASC only for the Purpose. The Materials shall not be used by ASC for commercial purposes or in human subjects.

4.         Reports . Recipient will furnish and provide Dara BioSciences, Inc. with a written summary of the experiments conducted by Recipient during the Research Program within thirty (30) days of the conclusion of the Research Program or the expiration of the Term, whichever is sooner (hereinafter, the results of the Research Program and any experiments and analysis thereof conducted by Recipient shall be referred to collectively as the "Results"). The documented Results shall be sent to John Didsbury, CSO, Dara BioSciences, Inc.

5.         Confidential Information . The Parties agree that, during the Term and following the expiration of this Agreement as hereinafter provided for, they shall not use, except as needed for the purposes of this Agreement or expressly permitted under this Agreement or disclose to any third party, any Confidential Information of the other Party without the prior written consent of the Party providing the Confidential Information. For purposes of this Agreement, "Confidential Information" means all information, in whatever format or medium delivered, reagents, tangible materials, procedures, data, results, conclusions, know-how, experience, trade secrets, or other proprietary information disclosed or provided by either of the Parties (the "Disclosing Party") to the other (the "Receiving Party") in connection with this Agreement, including without limitation the Research Program that pertains to the Materials. For purposes of this section, the Results shall be considered the Confidential Information of Dara BioSciences, Inc., with ASC being treated as the Receiving Party. The Receiving Party shall have no obligations with respect to any portion of Confidential Information that the Receiving Party can establish:

(a)        is or later becomes available to the public by use, publication or the like, through no fault of the Receiving Party; or

(b)        is obtained from a third party who was not bound by a duty of confidentiality and had the legal right to disclose the same to the Receiving Party; or

(c)        is already in the possession of the Receiving Party, predating generation of the Confidential Information under this Agreement or receipt of Confidential Information from the Disclosing Party, as evidenced by reasonable written documentation in existence prior to the date hereof; or

(d)        is independently developed by the Receiving Party without making use of Confidential Information from the Disclosing Party, as evidenced by reasonable written documentation in existence at the time of development.

6.         Permitted Disclosures . Notwithstanding the obligations in Section 5:

(a)        The Receiving Party may disclose Confidential Information of the Disclosing Party to its employees and agents, but only to the extent required to accomplish the purposes of this Agreement and only if such employees and agents to whom disclosure is to be made are bound by the duties of confidentiality substantially similar to, but in any event not less stringent than, those herein contained or who agree in writing to hold in confidence and not make use of such Confidential Information for any purpose other than as permitted by this Agreement on terms at least equivalent in scope to those set forth in this Agreement; and

            (b) &n


 
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