drugset / Trial / NCT01646671

Safety and Tolerability and Efficacy of LCZ696 in Japanese Severe Hypertensive Patients

NCT01646671

Phase 3 Completed 35 enrolled Novartis Pharmaceuticals
Non-randomizedSingle-groupOpen-labelTreatment

Summary

This study assessed the safety, tolerability, and efficacy of LCZ696 in severe hypertensive Japanese patients

Timeline

Start
2012-07
Primary completion
2013-02
Completion
2013-02

Drugs

EvaluationDrugModalityDoseRoute
Subject LCZ696 Unknown 200 mg
Subject LCZ696 Unknown 400 mg

Indications