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Study to Evaluate Effects of INL1 in Patients With Heart Failure and Reduced Ejection Fraction — TRACER-HF  

Heart Failure Clinical Trial

Official title:
A Randomized, Double-Blind, Placebo-Controlled Study to Evaluate the Effects of INL1 in Patients With Heart Failure and Reduced Ejection Fraction

Clinical Trial Summary

This is a multicenter, randomized, double-blind, placebo-controlled, dose-response trial in patients with chronic stable Heart Failure (HF) and reduced Left Ventricular Ejection Fraction (LVEF) to evaluate the efficacy and safety of three INL1 doses compared with placebo. Patients will be treated for approximately 12 weeks with one of three INL1 doses: 50 mg, 150 mg, 300 mg, or, placebo capsules, taken twice daily (BID).

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT03875183
Study type Interventional
Source Innolife Co., Ltd.
Contact Study Director
Phone 862-259-4382
Email daniel.qi@vita-spes.com
Status Recruiting
Phase Phase 2
Start date January 20, 2020
Completion date January 2023
View Details
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