Last updated on April 2019

Study to Evaluate the Efficacy and Safety of Belviq XR in Conjunction With Lifestyle Modification for Weight Loss in Obese Adolescents Age 12 to 17 Years


Brief description of study

This study will be conducted to demonstrate weight loss efficacy by change in body mass index (BMI) and safety in adolescents age 12 to 17 years (inclusive) during 52 weeks of treatment with Belviq XR 20 milligrams (mg) administered once daily (QD) as compared to placebo.

Clinical Study Identifier: NCT03338296

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The Center for Pharmaceutical Research

Kansas City, MO United States
4.26miles
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Recruitment Status: Open


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