drugset / Trial / NCT02862600

Open-Label Study of Perhexiline in Patients With Hypertrophic Cardiomyopathy and Moderate to Severe Heart Failure

NCT02862600 ↗

Phase 2 Terminated 35 enrolled Heart Metabolics Limited
NaSingle-groupOpen-labelTreatment

Summary

The purpose of this study is to evaluate the effect of perhexiline on exercise performance (efficacy) and safety in patients with hypertrophic cardiomyopathy and moderate-to-severe heart failure following dosing for 16 weeks.

Timeline

Start
2016-08-01
Primary completion
2017-04-28
Completion
2017-05-22

Outcome

Outcome not reported

Stopped: “Lack of Efficacy”

Drugs

EvaluationDrugModalityDoseRoute
Subject Perhexiline Small molecule — Oral