drugset / Trial / NCT03875183

Study to Evaluate Effects of INL1 in Patients With Heart Failure and Reduced Ejection Fraction

NCT03875183 ↗

Phase 2 Unknown 200 enrolled Innolife Co., Ltd.
RandomizedParallel-groupQuadruple-blindTreatment

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).

Timeline

Start
2020-01-20
Primary completion
2022-12
Completion
2023-01

Drugs

EvaluationDrugModalityDoseRoute
Subject INL1 Unknown 50 mg —
Subject INL1 Unknown 150 mg —
Subject INL1 Unknown 300 mg —

Indications