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First Amendment to Cornerstone License Agreement

License Agreement

First Amendment to Cornerstone License Agreement | Document Parties: CORNERSTONE THERAPEUTICS INC | Cornerstone Biopharma, Inc | Pharmaceutical Innovations, LLC You are currently viewing:
This License Agreement involves

CORNERSTONE THERAPEUTICS INC | Cornerstone Biopharma, Inc | Pharmaceutical Innovations, LLC

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Title: First Amendment to Cornerstone License Agreement
Date: 11/5/2008
Industry: Biotechnology and Drugs     Sector: Healthcare

First Amendment to Cornerstone License Agreement, Parties: cornerstone therapeutics inc , cornerstone biopharma  inc , pharmaceutical innovations  llc
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Exhibit 10.13

First Amendment to Cornerstone License Agreement

     This First Amendment to Cornerstone License Agreement (“Amendment”) is made and entered into on August, 10, 2007 (“Effective Date”), by and between Pharmaceutical Innovations, LLC (hereinafter referred to as “PI”) and Cornerstone Biopharma, Inc. (hereinafter referred to as “Cornerstone”).

Recitals :

     A. PI and Cornerstone entered into that certain Cornerstone License Agreement dated August 31, 2006 (“Agreement”), whereby Cornerstone secured from PI an exclusive license in the United States and a nonexclusive license in all other markets to manufacture, package, market, distribute and otherwise exploit the Licensed Products (as defined in the Agreement) on a worldwide basis.

     B. The parties desire to amend the Agreement as set forth in this Amendment.

NOW, THEREFORE, the undersigned hereby agree as follows:

 

     1.

 

The effective date of this Amendment shall be the Effective Date.

 

 

 

 

 

     2.

 

Section 1.10 of the Agreement is hereby deleted in its entirety and replaced with the following:

 

 

 

 

 

 

 

“1.10. “Licensed Products” shall mean the following prescription day-night products which fall within the scope of one or more valid claims of any PI Patent: (i) a product (which may be known as AlleRx PE) consisting of 40 mg. phenylephrine/2.5 mg. methscopolamine nitrate, for daytime use and 10 mg. phenylephrine/8 mg. chlorpheniramine maleate/2.5 mg. methscopolamine nitrate for nighttime use; (ii) a product (which may be known as AlleRx HC) consisting of [***] and (iii) a product consisting of 120 mg. pseudoephedrine/2.5 mg. methscopolamine nitrate, for daytime use and 8mg. chlorpheniramine maleate/2.5 mg. methscopolamine nitrate/an attenuated dose of pseudoephedrine or phenylephrine for nighttime use HCL for nighttime use.”

 

 

 

 

[***]

 

Confidential portions of the exhibit have been omitted and filed separately with the Securities and Exchange Commission.


 

 

 

3.

 

Section 4.03 of the Agreement is hereby deleted in its entirety and replaced with the following:

 

 

 

 

 

 

 

“4.03.(a) With respect to the License Product referenced in Section 1.10(i) hereof, Cornerstone shall pay to PI Minimum Royalty Payments equal to One Hundred Fifty Thousand Dollars ($150,000) per Calendar Year for the term of this Agreement beginning with Calendar Year 2007 and ending at the beginning of the Seven Year Period (such Minimum Royalty Payments to be pro rated for periods of less than twelve months.)

 

 

 

 

 

 

 

4.03(b) With respect to the Licensed Products referenced in Section 1.10(ii) and Section 1.10(iii) hereof, Cornerstone shall pay to PI (A) no Minimum Royalty Paym


 
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