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NCT06122779
Study to Evaluate Safety, Tolerability and Drug Levels of BMS-986435/MYK-224 in Participants With Heart Failure With Preserved Ejection Fraction (HFpEF)
Conditions: Heart Failure
Sex: All
Ages: 40 Years – 85 Years
Healthy volunteers: No
Phase: PHASE2
Enrollment: 208
Sponsor: Bristol-Myers Squibb
Location: University of Alabama at Birmingham Birmingham Alabama
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).
Eligibility Criteria
Inclusion Criteria
\- Adult participants with stable, symptomatic HFpEF with a normal heart pumping ability.
Exclusion Criteria
* Participants must not have a known diagnosis of obstructive or genetic hypertrophic cardiomyopathy or infiltrative/storage disorder such as cardiac amyloidosis, or any other acute or serious condition that could interfere with assessments during the study or may pose a risk to the participant.
* Other protocol-defined Inclusion/Exclusion criteria apply.
Source: ClinicalTrials.gov (NCT06122779). StuddyBuddy aggregates publicly available trial information.