drugset / Trial / NCT07547540

A Study of LY3971297 in Participants With Heart Failure

NCT07547540 ↗

Phase 1 Not yet recruiting 90 enrolled Eli Lilly and Company
RandomizedParallel-groupSingle-blindTreatment

Summary

The main purpose of this study is to assess how well LY3971297 is tolerated and what side effects may occur in participants with heart failure with preserved ejection fraction (HFpEF) and participants with heart failure with reduced ejection fraction (HFrEF). Blood tests will be performed to investigate how the body processes the study drug and how the study drug affects the body. For each participant, the study will last about 2 months and will include 1 inpatient visit lasting approximately 4 days and 5 outpatient visits.

Timeline

Start
2026-08
Primary completion
2027-11
Completion
2027-11

Drugs

EvaluationDrugModalityDoseRoute
Subject LY3971297 Unknown — Subcutaneous