VI-0521
Drugphentermine 15 mg and topiramate 92 mg, po once daily
NCT Number: NCT00553787
The purpose of this study is to evaluate the efficacy and safety of VI0521 compared to placebo in treatment of obesity in an adult population with obesity related co-morbid conditions.
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Notify Me18 year–70 year
All sexes
Interventional
Phase 3
Research Site, Birmingham, Alabama, United States
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
phentermine 15 mg and topiramate 92 mg, po once daily
Time frame: Baseline to 56 weeks
Time frame: Baseline to 56 weeks
VIVUS LLC
Industry
A Phase III Randomized, Double-Blind, Placebo Controlled Multicenter Study to Determine the Safety and Efficacy of VI-0521 in the Treatment of Obesity in Adults With Obesity-Related Co-Morbid Conditions
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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