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.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Enrollment
2,487
Research Site
Birmingham, Alabama, United States
Research Site
Ridgefield, Connecticut, United States
Research Site
New York, New York, United States
Research Site
Durham, North Carolina, United States
Percent Weight Loss From Baseline to Week 56
Time frame: Baseline to 56 weeks
Percentage of Subjects With a Weight Loss of at Least 5% at Week 56 With LOCF
Time frame: Baseline to 56 weeks
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Research Site
Toledo, Ohio, United States
Research Site
Austin, Texas, United States