drugset / Trial / NCT06017609

Evaluate Efficacy, Safety and Tolerability of JTT-861 in Subjects With Heart Failure With Reduced Ejection Fraction

NCT06017609 ↗

Phase 2 Completed 314 enrolled Akros Pharma Inc. ICON Clinical Research · collab
RandomizedParallel-groupQuadruple-blindTreatment

Summary

This study will evaluate the efficacy, safety, tolerability and pharmacokinetics of JTT-861 administered once daily for 12 weeks in subjects with heart failure with reduced ejection fraction (HFrEF) who are on a stable, guideline-directed medical therapy for heart failure.

Timeline

Start
2023-12-20
Primary completion
2026-05-18
Completion
2026-05-18

Drugs

EvaluationDrugModalityDoseRoute
Subject JTT-861 Unknown — Oral

Indications