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Amendment #2 To License Agreement 2003-03-0433

License Agreement

Amendment #2

To

License Agreement 2003-03-0433
 | Document Parties: OCCULOGIX, INC. |  The Regents of The University of California You are currently viewing:
This License Agreement involves

OCCULOGIX, INC. | The Regents of The University of California

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Title: Amendment #2 To License Agreement 2003-03-0433
Date: 3/15/2007

Amendment #2

To

License Agreement 2003-03-0433
, Parties: occulogix  inc. ,  the regents of the university of california
50 of the Top 250 law firms use our Products every day

 

***Section 4 of this Amendment has been omitted pursuant to a request for confidential treatment and has been filed separately with the U.S. Securities and Exchange Commission.

 

Amendment #2

To

License Agreement 2003-03-0433

 

This amendment #2 ("Amendment #2") is made by and between Ocusense, Inc., a Delaware corporation, having an address at 1820 Holmby Avenue, #4 Los Angeles, CA 90025 ("LICENSEE") and The Regents of The University of California, a California corporation having its statewide administrative offices at 1111   Franklin Street, Oakland, California 94607-5200 ("UNIVERSITY"), represented by its San Diego campus having an address at University of California, San Diego, Technology Transfer & Intellectual Property Services, Mail-code 0910, 9500 Gilman Drive, La Jolla, California 92093-0910 ("UCSD").

 

This Amendment #2 is effective on the date of the last signature ("Effective Date").

 

RECITALS

 

WHEREAS, LICENSEE and UNIVERSITY previously entered into License Agreement #2003-03-0433 ("License") as of March 12, 2003 for the commercial development of UCSD invention disclosure SD2002- 180 titled, "Volume Independent Tear Film Osmometer" ("Invention"), and have previously entered into Amendment No.1 to the License Agreement effective June 9, 2003;

 

WHEREAS, LICENSEE attests that as of the Effective Date no sublicenses to License have been granted;

 

WHEREAS, LICENSEE attests that the first Licensed Product under License which LICENSEE brings to market will require Food and Drug Administration (FDA) approval;

 

WHEREAS, LICENSEE has made successful progress to date in developing Invention for commercial use;

 

WHEREAS, in its efforts to develop market opportunities for the Invention, LICENSEE has requested certain revisions and/or clarifications to the License so as to facilitate LICENSEE's establishment of meaningful distribution channels and strategic partnerships, furthering the likelihood of realizing broad commercial markets for Invention;

 

WHEREAS, UNIVERS


 
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