drugset / Trial / NCT07667803

A Master Protocol to Investigate Efficacy and Safety of Elecoglipron in Participants With Obesity or Overweight With or Without T2DM

NCT07667803

Phase 3 Recruiting 4500 enrolled AstraZeneca
RandomizedParallel-groupTriple-blindTreatment

Summary

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).

Timeline

Start
2026-06-29
Primary completion
2028-07-31
Completion
2029-07-30

Drugs

EvaluationDrugModalityDoseRoute
Subject Elecoglipron Unknown Oral

Indications

No indication recorded.