drugset / Trial / NCT06987695

Efficacy and Safety of Maridebart Cafraglutide in Adult Participants in Japan Who Have Obesity Disease

NCT06987695

Phase 3 Active not recruiting 279 enrolled Amgen
RandomizedParallel-groupDouble-blindTreatment

Summary

The primary objective of this study is to demonstrate that maridebart cafraglutide is superior to placebo for percent change in body weight and proportion of participants with ≥ 5% reduction in body weight.

Timeline

Start
2025-06-13
Primary completion
2027-04-27
Completion
2027-07-21

Drugs

EvaluationDrugModalityDoseRoute
Subject Maridebart Cafraglutide Unknown Subcutaneous

Indications