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AMENDMENT #3 (FEBRUARY 2005 LICENSE AGREEMENT)

License Agreement

AMENDMENT #3 (FEBRUARY 2005 LICENSE AGREEMENT) | Document Parties: ROUGHNECK SUPPLIES INC. | Columbia University | Omnimmune Corp You are currently viewing:
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ROUGHNECK SUPPLIES INC. | Columbia University | Omnimmune Corp

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Title: AMENDMENT #3 (FEBRUARY 2005 LICENSE AGREEMENT)
Date: 8/12/2008

AMENDMENT #3 (FEBRUARY 2005 LICENSE AGREEMENT), Parties: roughneck supplies inc. , columbia university , omnimmune corp
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Exhibit 10.11

 

AMENDMENT #3

(FEBRUARY 2005 LICENSE AGREEMENT)

 

 

This amendment #3, effective as of the 31 st day of January 2007 (“Third Amendment Effective Date”), amends the February 1, 2005 License Agreement entered into and between The Trustees of Columbia University in the City of New York, a New York corporation located at 116 th street and Broadway, New York, New York, 10027 (“Columbia”), and Omnimmune Corp., a Texas corporation located at 4600 Post Oak Place, Suite 352, Houston, Texas 77027 (“Company”), as amended on March 29, 2005 and June 10, 2005 (collectively, the “Agreement”) according to the following terms and conditions:

 

1)  

Section 3a(ii)(a) is amended by replacing the entirety of this section with the following:

 

“$25,000 by May 1, 2007, and”

 

2)  

Section 3e is hereby amended by replacing the entirety of this section with the following:

 

“e.           License Maintenance Fees – Company shall pay annual license maintenance fees according to the schedule below:

$10,000 on or before May 1, 2007;

$20,000 on or before May 1, 2008;

$35,000 on or before May 1, 2009;

$50,000 on or before May 1, 2010; and $40,000 each first of May thereafter.”

 

3)  

Section 6a(i) is amended by replacing the entirety of this section with the following:

 

“Before February 1, 2008, Company and/or its Sublicensees or Affiliates shall have spent at least four hundred thousand dollars ($400,000) on the direct research and development of Licensed Product(s) in the Field.”

 

4)  

Section 6a(iii) is amended by replacing the entirety of this section with the following:

 

“Before February 1, 2010, Company and/or its Sublicensees or Affiliates shall have spent at least $2,500,000 on the direct research and development of Licensed Product(s) in the Field.”

 

5)  

Section 6a(iv) is amended by replacing the entirety of this section with the following:

 

“(iv)           Diagnosis

 

(a)   Company and/or its Sublicensees or Affiliates shall file an application with the FDA for at least one (1) Licensed Product for diagnosis


 
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