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Rechercher Study Connect
  • NCT06122779

Recruiting

Study to Evaluate Safety, Tolerability and Drug Levels of BMS-986435/MYK-224 in Participants With Heart Failure With Preserved Ejection Fraction (HFpEF) - CV029-1001

Mis à jour: 18 octobre, 2024   |   ClinicalTrials.gov

Résumé imprimable

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SÉLECTIONNER LA LANGUE

Détails de l’essai

  • Phase 2

    Phase

  • Sexe(s)

  • 40-90

    Tranche d’âge

  • 30

    Site(s)

  • Recruiting

Options de traitement

Bras de l’étude
INTERVENTION ASSIGNÉE
Experimental: BMS-986435
Drug: BMS-986435
Placebo Comparator: Placebo
Other: Placebo

Principaux critères d’éligibilité

Key Inclusion Criteria: - Adult participants with stable, symptomatic HFpEF with a normal heart pumping ability Key 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 Note: Other protocol-defined inclusion/exclusion criteria apply

Nous vous recommandons vivement de contacter BMS pour signaler les effets secondaires (événements indésirables)
Les effets secondaires (événements indésirables) et les autres événements à signaler sont définis ici
Signaler des plaintes concernant des effets indésirables (effets indésirables) ou des produits: Informations médicales