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SEQUEL Trial Results for Qnexa® Published in AJCN Show 10% Sustained Weight Loss Over 2 Years
Date:12/8/2011

FDA's CRL or CHMP's 120-day questions, the FDA's requests stemming from the end-of-review meeting or the results of the retrospective observational study of fetal outcomes in infants born to mothers exposed to topiramate during pregnancy and subsequent meetings and communications will be sufficient to satisfy the FDA or CHMP's safety concerns, that the FDA or foreign authorities will not require us to conduct any additional prospective studies or retrospective observational studies, or that any product will receive regulatory approval for any indication or prove to be commercially successful.  VIVUS does not undertake an obligation to update or revise any forward-looking statements.  Investors should read the risk factors set forth in VIVUS' Form 10-K for the year ending December 31, 2010, and periodic reports filed with the Securities and Exchange CommissionCONTACT:  

 VIVUS, Inc.Media Relations:GolinHarrisTimothy E. Morris

 

Susan Brophy Chief Financial Officer

 

sbrophy@golinharris.com 650-934-5200

 

312-729-4359 

 

  Investor Relations:The Trout Group 

 

Brian Korb 

 

bkorb@troutgroup.com 

 

646-378-2923 


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