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AMENDMENT TO LICENSE AGREEMENT

License Agreement

AMENDMENT TO LICENSE AGREEMENT | Document Parties: REPLIDYNE, INC. | DAIICHI SUNTORY PHARMA CO., LTD You are currently viewing:
This License Agreement involves

REPLIDYNE, INC. | DAIICHI SUNTORY PHARMA CO., LTD

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Title: AMENDMENT TO LICENSE AGREEMENT
Governing Law: Delaware     Date: 4/5/2006
Industry: Biotechnology and Drugs     Sector: Healthcare

AMENDMENT TO LICENSE AGREEMENT, Parties: replidyne  inc. , daiichi suntory pharma co.  ltd
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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 406 of the Securities Exchange Act Of 1933, as amended.

Exhibit 10.14.1

AMENDMENT

TO

LICENSE AGREEMENT

     This Amendment (the “ Amendment ”) is entered into as of April 5, 2005 (the “Effective Date” ) to modify the terms of the License Agreement (the “ License Agreement ”) dated as of March 15, 2004 by and between DAIICHI SUNTORY PHARMA CO., LTD., a corporation organized and existing under the laws of Japan and having its registered office at 7-2, Kojimachi 5-chome, Chiyoda-ku, Tokyo 102-8530, Japan (hereinafter referred to as “ DSP ”) and REPLIDYNE, INC., a corporation organized and existing under the laws of the State of Delaware, having its principal business office at 1450 Infinite Drive, Louisville, Colorado 80027, U.S.A. (hereinafter referred to as “ REPLIDYNE ”). DSP and REPLIDYNE are sometimes referred to collectively herein as the “ Parties ” or individually as a “ Party.

WITNESSETH:

WHEREAS , DSP and REPLIDYNE have signed a License Agreement regarding the development and commercialization of Faropenem Daloxate for the United States and Canadian markets; and

WHEREAS , DSP and REPLIDYNE have entered into the License Agreement regarding the development and commercialization of Faropenem Daloxate for the United States and Canadian markets; and

WHEREAS , since the License Agreement was signed, plans for the development and commercialization of Faropenem Daloxate have changed; and

WHEREAS, in light of those developments, the parties agree to revise certain economic terms of the License Agreement as indicated below.

NOW, THEREFORE, for and in consideration of the premises and covenants contained herein, DSP and REPLIDYNE agree to amend the License Agreement as written below.

1. Section 6.1 “License Fees” shall be replaced in its entirety. The new Section 6.1 shall be written as:

“6.1 License Fees. In consideration of the rights and benefits granted hereunder, REPLIDYNE shall pay to DSP the following license fees in Japanese Yen (hereinafter referred to as “ JPY ”):

 

(a)

 

Four hundred million Japanese Yen (JPY 400,000,000) within thirty (30) days after execution of this Agreement;

 


 

 

 

(b)

 

[ *** ] Japanese Yen (JPY [ *** ]) within ninety (90) days after the NDA filing in the Territory [ *** ] ;

 

 

 

 

 

(c)

 

[ *** ] Japanese Yen (JPY [ *** ]) within ninety (90) days after the NDA approval in the Territory of [ *** ] ;

 

 

 

 

 

(d)

 

[ *** ] .

 

 

 

 

 

(e)

 

[ *** ] ;

 

 

 

 

 

(f)

 

Five hundred million Japanese Yen (JPY 500,000,000) within ninety (90) days after the Launch, provided, however, [ *** ] ;

 

 

 

 

 

(g)

 

[ *** ] .

[ **


 
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