Elecoglipron
DrugElecoglipron tablet
NCT Number: NCT07761117
This is a Phase III, randomized, double-blind, parallel-group, placebo-controlled, multicenter study to investigate CV outcomes with elecoglipron compared with placebo, in adults with heart failure with preserved ejection fraction (HFpEF)/heart failure with mildly reduced ejection fraction (HFmrEF), irrespective of T2DM status, and who are on background dapagliflozin in addition to other background standard of care.
Trial opening soon.
Get Notified18 year and older
All sexes
Interventional
Phase 3
Research Site, Buenos Aires, Argentina
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Elecoglipron tablet
Placebo tablet
Time frame: Up to 42 months
Time to first event of the composite of:
CV death HHF Urgent HF visit
Time frame: Up to 42 months
Total occurrences (first and recurrent) of HF events HHF Urgent HF visit
Time frame: Baseline and 52 weeks
Change from baseline to Week 52
Time frame: Up to 42 months
Time to first event of the composite of All-cause death HHF MI Stroke
Contact information is provided by the study sponsor or research team.
AstraZeneca
Industry
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)
Acronym: Elevate-HF
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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