drugset / Trial / NCT02226120

Safety and Tolerability During Open-label Treatment With LCZ696 in Patients With CHF and Reduced Ejection Fraction

NCT02226120

Phase 3 Completed 1980 enrolled Novartis Pharmaceuticals
NaSingle-groupOpen-labelTreatment

Summary

The purpose of this study was to collect safety and tolerability data on LCZ696 in eligible PARADIGM-HF patients who received open-label investigational drug. The parent PARADIGM-HF (NCT01035255) trial was terminated early due to compelling efficacy of LCZ696 in patients with heart failure with reduced ejection fraction (HFrEF) after the final pre-specified interim analysis in March 2014.

Timeline

Start
2014-10-16
Primary completion
2017-12-28
Completion
2017-12-28

Drugs

EvaluationDrugModalityDoseRoute
Subject LCZ696 Unknown 200 mg