Study identifier:D7261C00005
ClinicalTrials.gov identifier:NCT07662213
EudraCT identifier:N/A
CTIS identifier:N/A
A Randomized, Open-label, Parallel-group Phase III Study to Evaluate the Efficacy, Safety, and Tolerability of Elecoglipron Compared with Oral Semaglutide in Adults with Type 2 Diabetes Mellitus (Eluminate-2)
Type 2 Diabetes Mellitus
Phase 3
no
Elecoglipron, Semaglutide
All
1200
Interventional
18 Years +
Allocation: Randomized
Endpoint Classification: -
Intervention Model: Parallel
Masking: -
Primary Purpose: Treatment
Verified 01 May 2026 by AstraZeneca
AstraZeneca
-
No locations available
| Arms | Assigned Interventions |
|---|---|
| Experimental: Elecoglipron Participants will receive elecoglipron dose XX mg administered orally once daily. | Drug: Elecoglipron Elecoglipron is administered orally once daily. |
| Active Comparator: Semaglutide Participants will receive semaglutide dose XX mg administered orally once daily. | Drug: Semaglutide Semaglutide is administered orally once daily. |