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Data on VIVUS' QNEXA to be Presented in Six Posters at The Obesity Society's Annual Meeting
Date:10/7/2010

MOUNTAIN VIEW, Calif., Oct. 7 /PRNewswire/ -- VIVUS, Inc. (Nasdaq: VVUS) today announced that data on QNEXA®, an investigational drug candidate, are highlighted in six poster presentations at the 28th Annual Scientific Meeting of The Obesity Society, being held October 8-12, 2010 in San Diego, California.

Following are details about the poster presentations:

The Obesity Society 28th Annual Scientific Meeting at The San Diego Convention Center in San Diego, CA

All six posters will be presented in Poster Session #2 (Hall H) on Sunday, October 10, 2010 from 9:30 am to 1:45 pm and from 3:15 pm to 6:30 pm.  

Presenters will be at their posters from 12:30 pm to 1:30 pm. Presenter:

Wesley W. Day, PhDAuthors:

Day, Najarian, Troupin, Tam, PetersonTitle:

Low-Dose, Controlled-Release Phentermine/Topiramate Reduces Hunger and Increases Satiety, Leading to Weight Loss in Overweight/Obese Adults (Abstract # 212898; Poster # 490-P)Presenter:

Kishore M. Gadde, MDAuthors:

Gadde, Peterson, DayTitle:

Clinically Meaningful Weight-Loss Outcomes With Low-Dose, Controlled-Release Phentermine/Topiramate in Overweight/Obese Subjects (Abstract # 212885; Poster #486-P)Presenter:

Dympna Gallagher, EdDAuthors:

Gallagher, Punyanitya, Bowden, PetersonTitle:

Low-Dose, Controlled-Release Phentermine/Topiramate Reduces Adiposity, Improves Cardiometabolic Risk in Overweight/Obese Patients (Abstract # 212891; Poster # 488-P)Presenter:

W. Timothy Garvey, MDAuthors:

Garvey, Peterson, Troupin, BowdenTitle:

Low-Dose, Controlled-Release Phentermine/Topiramate for Weight Loss and Management of Type 2 Diabetes Mellitus (Abstract # 212889; Poster # 492-P)Presenter:

Samuel Klein, MDAuthors:

Klein, Najarian, DayTitle:

Weight Loss With Once-Daily, Low-Dose, Controlled-Rele
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SOURCE VIVUS, Inc.
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Related biology technology :

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6. VIVUS Announces Positive Results From Two Phase 3 Studies; Obese Patients on Qnexa Achieve Average Weight Loss up to 14.7% and Significant Improvements in Co-Morbidities
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