A Master Protocol to Investigate Efficacy and Safety of Elecoglipron in Participants With Obesity or Overweight With or Without T2DM
This master study protocol, Study D7260C00015, covers 2 independent, pivotal studies, Study 1 and Study 2. Each study is a global, randomized, double-blind, parallel-group, multicenter, Phase III study to assess the efficacy and safety of elecoglipron compared with placebo adjunct to diet and exercise for weight management, in adults living with obesity or overweight with at least one weight-related comorbidity, and without T2DM (Study 1) or with T2DM (Study 2).
Conditions studied
Weight Management
About this study
This master study protocol, Study D7260C00015, covers 2 independent, pivotal studies, Study 1 and Study 2. Each study is a global, randomized, double-blind, parallel-group, multicenter, Phase III study to assess the efficacy and safety of elecoglipron compared with placebo adjunct to diet and exercise for weight management, in adults living with obesity or overweight with at least one weight-related comorbidity, and without T2DM (Study 1) or with T2DM (Study 2).
Interventions
- Drug: Elecoglipron — Elecoglipron film-coated tablet once daily
- Drug: Placebo — Placebo matching elecoglipron film-coated tablet once daily
Primary outcomes
- Percent body weight loss (72 weeks)
Eligibility information
Study locations
- Research Site, Birmingham, Alabama 35205 United States
- Research Site, Dothan, Alabama 36305 United States
- Research Site, Chandler, Arizona 85225 United States
- Research Site, Sun City, Arizona 85373 United States
- Research Site, Little Rock, Arkansas 72205 United States
- Research Site, Lynwood, California 90262 United States
- Research Site, Rolling Hills Estates, California 90274 United States
- Research Site, Sacramento, California 95821 United States
- Research Site, Arvada, Colorado 80002 United States
- Research Site, New Haven, Connecticut 06519 United States
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Source: ClinicalTrials.gov. Record last refreshed by Varda Clinical: 2026-09-27.