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Re: (1) Expanded and Amended Thymosin Alpha 1 License, Distributorship and Supply Agreement signed by and between SciClone Pharmaceuticals International Ltd ("SPIL") and Sigma-Tau Industrie Farmaceutiche Riunite S.p.A. ("STI") on March 3, 2000 as amended (collectively, the "Thymosin Alpha License

Requirements Supplier Agreement

Re:    (1) Expanded and Amended Thymosin Alpha 1 License, Distributorship and Supply Agreement signed by and between SciClone Pharmaceuticals International Ltd ( You are currently viewing:
This Requirements Supplier Agreement involves

SCICLONE PHARMACEUTICALS INC

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Title: Re: (1) Expanded and Amended Thymosin Alpha 1 License, Distributorship and Supply Agreement signed by and between SciClone Pharmaceuticals International Ltd ("SPIL") and Sigma-Tau Industrie Farmaceutiche Riunite S.p.A. ("STI") on March 3, 2000 as amended (collectively, the "Thymosin Alpha License
Date: 4/1/2009
Industry: Biotechnology and Drugs     Sector: Healthcare

Re:    (1) Expanded and Amended Thymosin Alpha 1 License, Distributorship and Supply Agreement signed by and between SciClone Pharmaceuticals International Ltd (
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Exhibit 10.2

[Sigma-Tau Industrie Farmaceutiche Riunite S.p.A. Letterhead]

Sede: Viale Shakespeare, 47 – 00144 Roma

tel. +39 06 592.64.43 – +39 06 592.66.00

Stabilimento: Via Pontina km 30,400

00040 Pomezia (RM) Italia – tel. +39 06 9139

Pomezia, March 30, 2009

SciClone Pharmaceuticals, Inc.

950 Tower Lane

Foster City, CA 94404

Attention: Friedhelm Blobel

Dear Sirs:

Re:    (1) Expanded and Amended Thymosin Alpha 1 License, Distributorship and Supply Agreement signed by and between SciClone Pharmaceuticals International Ltd (“SPIL”) and Sigma-Tau Industrie Farmaceutiche Riunite S.p.A. (“STI”) on March 3, 2000 as amended (collectively, the “Thymosin Alpha License Agreement”); and (2) Other Business Matters pertaining to Thymosin Alpha 1 for the malignant melanoma indication.

The undersigned hereby agree that, upon execution hereof:

(1) SciClone Pharmaceuticals, Inc. (“SCLN”), with the approval of its Board of Directors, will cause SPIL, under the Thymosin Alpha 1 License Supply Agreement, to grant STI the rights, (i) to lead all future development activities for Thymosin Alpha 1 (as defined in the Thymosin Alpha License Agreement) with respect to Hepatitis C Virus indications in the Territory as defined in the Thymosin Alpha License Agreement, at STI’s costs; provided that if SPIL’s non-European interests will be materially affected by any negotiations in which STI participates then SPIL will have the right to participate in those negotiations, and (ii) to meet, correspond, and otherwise interact with the European regulatory agencies responsible for granting any approval necessary for the development of Thymosin Alpha 1 for the treatment of the Hepatitis C Virus regarding such development and any matters related thereto. STI will keep SPIL appropriately


 
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