drugset / Trial / NCT06793371

AMBER-HFpEF: Assessment of CK-4021586 in a Multi-Center, Blinded Evaluation of Safety and Tolerability Results in HFpEF

NCT06793371 ↗

Phase 2 Recruiting 60 enrolled Cytokinetics
RandomizedParallel-groupTriple-blindTreatment

Summary

This is a Phase 2 dose-finding study in adult participants with symptomatic HFpEF.

Timeline

Start
2025-02-06
Primary completion
2026-09
Completion
2026-09

Drugs

EvaluationDrugModalityDoseRoute
Subject CK-4021586 Unknown 150 mg Oral
Subject CK-4021586 Unknown 300 mg Oral
Subject CK-4021586 Unknown 450 mg Oral
Subject CK-4021586 Unknown 600 mg Oral