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NCT06122779 · ClinicalTrials.gov registry record · Phase 2

Study to Evaluate Safety, Tolerability and Drug Levels of BMS-986435/MYK-224 in Participants With Heart Failure With Preserved Ejection Fraction (HFpEF)

A Phase 2 study of Heart Failure, sponsored by Bristol-Myers Squibb.

Recruiting
Registry status
Phase 2
Development phase
208
Enrollment target
20
Study locations

NCT06122779: Recruiting Phase 2 study of Heart Failure, sponsored by Bristol-Myers Squibb.

NCT06122779 is a Phase 2 study of Heart Failure that is actively recruiting participants, run by Bristol-Myers Squibb. The registered enrollment target is 208 participants, below the 2,049-participant average among 397 other Heart Failure trials with a reported enrollment target (90% lower). The trial reports 20 study locations across 9 states. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT06122779, a Phase 2 study of Heart Failure, is actively recruiting participants, sponsored by Bristol-Myers Squibb.

RECRUITING
Registry status
Phase 2
Development phase
208 participants
Enrollment target
20
Study locations

Study Summary

The purpose of this study is to evaluate the safety, tolerability, and exposure-response (E-R) of BMS-986435/MYK-224 in participants with symptomatic Heart Failure with Preserved Ejection Fraction (HFpEF).

Conditions Studied

Interventions

  • OTHER Placebo
  • DRUG BMS-986435

Study Locations (20)

New York

  • Capital Cardiology Associates - Albany
  • Local Institution - 0105 - Brooklyn
  • Weill Cornell Medicine - New York
  • University of Rochester Medical Center - PPDS - Rochester
  • Rochester General Hospital Center for Clinical Research - Rochester
  • Laurelton Heart Specialist PC - MyClinical - PPDS - Rosedale

Florida

  • Ascension St. Vincent's Riverside Hospital - PPDS - Jacksonville
  • Local Institution - 0003 - Miami
  • University of Miami FL Miller School of Medicine -1120 NW 14th St - Miami

Georgia

  • Local Institution - 0014 - Atlanta
  • Local Institution - 0048 - Atlanta

Illinois

  • Bluhm Cardiovascular Institute of Northwestern - Chicago
  • Chicago Medical Research, LLC - Hazel Crest - Hazel Crest

Indiana

  • Ascension Medical Group St. Vincent - Indianapolis Heart Care - Indianapolis
  • Local Institution - 0045 - Indianapolis

Missouri

  • St. Louis Heart and Vascular - St Louis
  • Local Institution - 0043 - St Louis

Alabama

  • University of Alabama at Birmingham - Birmingham

Colorado

  • Colorado Heart and Vascular - Lakewood - Lakewood

Trial Details

FieldValue
Enrollment Target 208 participants
Start Date 2023-11-07
Est. Completion 2026-07-03
Phase Phase 2
Bristol-Myers Squibb

1,025 total trials

What NCT06122779 shows while recruiting

NCT06122779 is an interventional study that assigns participants to a tested intervention. The registered 208 participants enrollment target is mid-sized for trials with a published cap, below the 2,049-participant average among 397 other Heart Failure trials with a reported enrollment target (90% lower).

The record links to 1 condition, with Heart Failure appearing as the primary indexed condition, and to 2 interventions - of which Placebo is the first listed.

NCT06122779 names 20 study sites across 9 states, led by New York, Florida, Georgia.

Frequently Asked Questions

What is clinical trial NCT06122779 about?

NCT06122779 is a clinical study titled "Study to Evaluate Safety, Tolerability and Drug Levels of BMS-986435/MYK-224 in Participants With Heart Failure With Preserved Ejection Fraction (HFpEF)". The purpose of this study is to evaluate the safety, tolerability, and exposure-response (E-R) of BMS-986435/MYK-224 in participants with symptomatic Heart Failure with Preserved Ejection Fraction (HFpEF).

What is the current status of trial NCT06122779?

This trial is currently recruiting. It is a Phase 2 study. The enrollment target is 208 participants. The study started on 2023-11-07. Estimated completion is 2026-07-03.

What conditions does trial NCT06122779 study?

This clinical trial studies the following conditions: Heart Failure.

What interventions are being tested in trial NCT06122779?

The interventions under investigation include: Placebo (OTHER), BMS-986435 (DRUG).

Who is sponsoring clinical trial NCT06122779?

This trial is sponsored by Bristol-Myers Squibb, which has 1,025 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT06122779 being conducted?

This trial has 20 study locations across Alabama, Colorado, Florida, Georgia, Illinois. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Heart Failure

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Where NCT06122779's enrollment target sits among peer trials

208 161st of 397 higher than 236 of 397 other Heart Failure trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Heart Failure trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT06122779, the US trial registry maintained by the National Library of Medicine. NCT06122779 (mid enrollment · wide site footprint · recruiting) retrieved and formatted by PlainTrial, see methodology.