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

Heart Failure

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).

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Conditions de participation

  • Sexe:

    ALL
  • Âges admissibles:

    40 to 90

Critères de participation

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.

Lieu de l'étude

Hamilton General Hospital
Hamilton General Hospital
Hamilton, Ontario
Canada

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Primary Contact

Catherine Demers, Site 0007

Local Institution - 0011
Local Institution - 0011
Montreal, Quebec
Canada

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Local Institution - 0040
Local Institution - 0040
Toronto, Ontario
Canada

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Local Institution - 0035
Local Institution - 0035
Trois-Rivieres, Quebec
Canada

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Local Institution - 0037
Local Institution - 0037
Toronto, Ontario
Canada

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Local Institution - 0030
Local Institution - 0030
Toronto, Ontario
Canada

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Étude parrainée par
Bristol-Myers Squibb
Participants recherchés
Plus d'informations
ID de l'étude: NCT06122779