A study to investigate the efficacy and safety of elecoglipron in Asian participants with obesity or overweight with or without type 2 diabetes mellitus - Elecoglipron

Study identifier:D7260C00022

ClinicalTrials.gov identifier:NCT07775404

EudraCT identifier:N/A

CTIS identifier:N/A

Recruiting

Official Title

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)

Medical condition

obesity

Phase

Phase 3

Healthy volunteers

no

Study drug

Elecoglipron, Placebo

Sex

All

Estimated Enrollment

351

Study type

Interventional

Age

18 Years +

Date

Study Start Date: 21 Aug 2026
Estimated Primary Completion Date: 04 Jun 2027
Estimated Study Completion Date: 20 Apr 2028

Study design

Allocation: Randomized
Endpoint Classification: -
Intervention Model: Parallel
Masking: -
Primary Purpose: Treatment

Verification:

Verified 01 Jul 2026 by AstraZeneca

Sponsors

AstraZeneca

Collaborators

-

Inclusion and exclusion criteria