Study identifier:D7266C00001
ClinicalTrials.gov identifier:NCT07761117
EudraCT identifier:N/A
CTIS identifier:N/A
A Phase III, Randomized, Double-blind, Parallel-group, Placebo-controlled, Multicenter Study to Evaluate the Effect of Elecoglipron in Reducing Cardiovascular Outcomes in Participants with HFpEF and HFmrEF (Elevate-HF)
Heart Failure with Preserved Ejection Fraction (HFpEF), Heart failure with mildly reduced ejection fraction (HFmrEF)
Phase 3
no
Elecoglipron, Placebo
All
6950
Interventional
18 Years +
Allocation: Randomized
Endpoint Classification: -
Intervention Model: Parallel
Masking: -
Primary Purpose: Treatment
Verified 01 Jun 2026 by AstraZeneca
AstraZeneca
-
No locations available
| Arms | Assigned Interventions |
|---|---|
| Experimental: Elecoglipron Elecoglipron tablet once daily | Drug: Elecoglipron Elecoglipron tablet |
| Active Comparator: Placebo Placebo matching Elecoglipron tablet once daily | Drug: Placebo Placebo tablet |