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FIRST AMENDMENT TO THE EXCLUSIVE DISTRIBUTION AGREEMENT

Distribution Agreement

FIRST AMENDMENT TO THE EXCLUSIVE DISTRIBUTION AGREEMENT | Document Parties: HALOZYME THERAPEUTICS INC | BAXTER HEALTHCARE CORPORATION You are currently viewing:
This Distribution Agreement involves

HALOZYME THERAPEUTICS INC | BAXTER HEALTHCARE CORPORATION

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Title: FIRST AMENDMENT TO THE EXCLUSIVE DISTRIBUTION AGREEMENT
Date: 3/30/2005

FIRST AMENDMENT TO THE EXCLUSIVE DISTRIBUTION AGREEMENT, Parties: halozyme therapeutics inc , baxter healthcare corporation
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                                                                    EXHIBIT 10.2

 

                               CONFIDENTIAL TREATMENT REQUESTED - REDACTED COPY

 

  CONFIDENTIAL TREATMENT REQUESTED:   INFORMATION FOR WHICH CONFIDENTIAL TREATMENT

     HAS BEEN REQUESTED IS OMITTED AND NOTED WITH "***." AN UNREDACTED VERSION OF

      THIS DOCUMENT HAS BEEN SUBMITTED SEPARATELY TO THE SECURITIES AND EXCHANGE

                                                                     COMMISSION.

 

                              FIRST AMENDMENT TO THE

                        EXCLUSIVE DISTRIBUTION AGREEMENT

 

      This FIRST AMENDMENT TO THE EXCLUSIVE DISTRIBUTION AGREEMENT (this

"Amendment"), effective as of March 24, 2005, is entered into by and between

BAXTER HEALTHCARE CORPORATION with its principal place of business at One Baxter

Parkway, Deerfield, Illinois 60015-4633 ("Baxter"), and HALOZYME, INC. with its

principal place of business at 11588 Sorrento Valley Road, Suite 17, San Diego,

California 92121 ("Halozyme"), and is the first amendment to that EXCLUSIVE

DISTRIBUTION AGREEMENT (the "Distribution Agreement") between Baxter and

Halozyme that was entered into as of August 13, 2004.

 

      WHEREAS, the parties are in connection herewith entering into a

Development and Supply Agreement (the "Development and Supply Agreement") that

reflects the parties' ongoing efforts to develop and supply Initial Product(s)

and potentially Other Product(s) the active ingredient of which is human

recombinant PH20 hyaluronidase for certain indications; and

 

      WHEREAS, the parties wish to provide for a specific and consistent

definition and treatment of the Initial Product(s) and potentially Other

Product(s) pursuant to the terms of the Development and Supply Agreement and the

Distribution Agreement, the parties hereto agree to amend the Distribution

Agreement as follows:

 

"Product", as used in the Distribution Agreement, shall have the same meaning as

provided for "Initial Product(s)", as defined in the Development and Supply

Agreement;

 

"Improvements", as used in the Distribution Agreement, shall have the same

meaning as provided for "improvements" under the definition of "Initial

Product(s)", as defined in the Development and Supply Agreement;

 

"Other Products", as used in the Distribution Agreement, shall have the same

meaning as provided for "Other Products", as defined in the Development and

Supply Agreement;

 

The "Indemnification" provisions of the Development and Supply Agreement

(specifically Section 15, including Sub-sections 15.1-15.3) shall apply equally

to Products, Improvements and Other Products (individually and collectively

"Distributed Product(s)") under this Distribution Agreement, with "this

Agreement" referring to this Distribution Agreement, "API" referring to API

supplied to Baxter for the Production of Distributed Product(s), and "Product"

referring to Distributed Product(s).

 

Sub-sect


 
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