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RecruitingPhase 3

A Study to Investigate CV Outcomes With Elecoglipron Compared With Placebo in Adult Participants With HFpEF or HFmrEF

AstraZeneca · NCT07761117

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Key facts

Compensation
Not posted. Ask the study team before screening.
Who can join
Ages 18+ · All sexes
Healthy volunteers
Not accepted (a condition is required)
Study type
Interventional · Phase 3
Target enrollment
6950
US sites recruiting
9
Study start
August 24, 2026
Record last updated
September 28, 2026

Status re-checked against ClinicalTrials.gov within the last 12 hours.

What the study is about

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.

Being studied: Elecoglipron; Placebo

Conditions: Heart Failure With Preserved Ejection Fraction (HFpEF); Heart Failure With Mildly Reduced Ejection Fraction (HFmrEF)

Eligibility criteria

Copied from the official record. The study team makes the final decision at screening.

Show full criteria

Inclusion Criteria

  • Left ventricular ejection fraction (LVEF) of > 40% within 12 months prior to screening.
  • Structural heart disease evidence.
  • HF diagnosed with New York Heart Association (NYHA) Class II-IV at the time of screening.

Exclusion Criteria

  • BMI \<25 kg/m² at screening.
  • Diabetes exclusions:
  • History of type 1 diabetes.
  • HbA1c ≥10% at screening.
  • Currently receiving or anticipated to receive therapeutic intervention for diabetic retinopathy and/or macular edema.
  • more than 1 episode of severe hypoglycemic event within 180 days prior to screening, or hypoglycemia unawareness/poor recognition.
  • Renal exclusions:
  • On a prespecified renal replacement therapy, or eGFR below a prespecified threshold at screening
  • Cardiovascular exclusions:
  • Major cardiac surgery, coronary revascularization, valvular repair/replacement, AF/AFL ablation, CRT implantation, or ICD without CRT within 90 days prior to screening, or planned after randomization.
  • Heart failure due to infiltrative cardiomyopathy, active myocarditis, constrictive pericarditis, cardiac tamponade, genetic hypertrophic cardiomyopathy (including obstructive), or arrhythmogenic right ventricular cardiomyopathy/dysplasia.
  • GI exclusions:
  • Clinically significant upper GI condition affecting gastric emptying, drug absorption, or safety/tolerability interpretation; chronic use of drugs directly affecting GI motility; severe disease or prior surgery.
  • History of acute or chronic pancreatitis.
  • Endocrine exclusions:
  • History/ family history of medullary thyroid carcinoma (MTC) or multiple endocrine neoplasia type 2, or basal calcitonin ≥35 ng/L at screening.

Recruiting US locations

Study contacts (from the official record)

  • AstraZeneca Clinical Study Information Center · 1-877-240-9479 · information.center@astrazeneca.com
A Study to Investigate CV Outcomes With Elecoglipron Compared With… (NCT07761117) | Bored Studies