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Sanofi and Regeneron Launch Comprehensive Phase 3 Clinical Program With LDL Cholesterol-Lowering PCSK9 Antibody
Date:7/19/2012

e governmental authorities which may delay or restrict Regeneron's ability to continue to develop or commercialize Regeneron's product and drug candidates, competing drugs that may be superior to Regeneron's product and drug candidates, uncertainty of market acceptance of Regeneron's products and drug candidates, unanticipated expenses, the availability and cost of capital, the costs of developing, producing, and selling products, the potential for any license or collaboration agreement, including Regeneron's agreements with the Sanofi Group and Bayer HealthCare, to be canceled or terminated without any product success, and risks associated with third party intellectual property and pending or future litigation relating thereto.  A more complete description of these and other material risks can be found in Regeneron's filings with the United States Securities and Exchange Commission, including its Form 10-K for the year ended December 31, 2011 and Form 10-Q for the quarter ended March 31, 2012.  Regeneron does not undertake any obligation to update publicly any forward-looking statement, whether as a result of new information, future events, or otherwise, unless required by law.

Contacts:

Sanofi:

Media Relations
Marisol Péron
Tel: +33-(0)1-53-77-45-02
Mobile: +33(0)6-08-18-94-78
marisol.peron@sanofi.com

Investor Relations
Sébastien Martel
Tel: +33(0)1-53-77-45-45
IR@sanofi.com

Regeneron:

Media Relations
Peter Dworkin
Tel: +1-914-847-7640
peter.dworkin@regeneron.com

Investor Relations
Manisha Narasimhan, Ph.D.
Tel: +1-914-847-5126
manisha.narasimhan@regeneron.com



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SOURCE Sanofi and Regeneron Pharmaceuticals, Inc.
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