A Phase 2A, Double-blind, Randomized, Placebo-controlled, Multi-center Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of BMS-986435/MYK-224 in Participants With Heart Failure With Preserved Ejection Fraction (HFpEF)

Status: Recruiting

Phase of Trial: Phase II

Latest Information Update: 04 Apr 2025

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At a glance

Drugs MYK 224 (Primary)
Indications Heart failure
Focus Adverse reactions
Sponsors Bristol-Myers Squibb

Most Recent Events

10 Feb 2025 Planned number of patients changed from 48 to 198.
05 Dec 2024 Planned End Date changed from 22 Jan 2025 to 3 Jul 2026.
05 Dec 2024 Planned primary completion date changed from 22 Jan 2025 to 3 Jul 2026.

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