Study identifier:D7260C00022
ClinicalTrials.gov identifier:NCT07775404
EudraCT identifier:N/A
CTIS identifier:N/A
A Phase III, Randomised, Double-blind, Placebo-controlled, Multicentre Study to Evaluate the Efficacy and Safety of Elecoglipron in Asian Participants with Obesity or Overweight with or without Type 2 Diabetes Mellitus (EMBOLD-Asia)
obesity
Phase 3
no
Elecoglipron, Placebo
All
351
Interventional
18 Years +
Allocation: Randomized
Endpoint Classification: -
Intervention Model: Parallel
Masking: -
Primary Purpose: Treatment
Verified 01 Jul 2026 by AstraZeneca
AstraZeneca
-
No locations available
| Arms | Assigned Interventions |
|---|---|
| Experimental: Arm 1 - Dose 1 Active IMP | Drug: Elecoglipron Elecoglipron film coated tablet once daily |
| Experimental: Arm 2 - Dose 2 Active IMP | Drug: Elecoglipron Elecoglipron film coated tablet once daily |
| Placebo Comparator: Arm 3 - Placebo Placebo matching elecoglipron | Drug: Placebo Placebo matching elecoglipron film-coated tablet once daily |