drugset / Trial / NCT01593787

Safety and Tolerability and Efficacy of LCZ696 in Japanese Hypertensive Patients With Renal Dysfunction

NCT01593787

Phase 3 Completed 32 enrolled Novartis Pharmaceuticals
Non-randomizedSingle-groupOpen-labelTreatment

Summary

This study assessed the safety, tolerability, and efficacy of LCZ696 in hypertensive patients with renal dysfunction.

Timeline

Start
2012-05
Primary completion
2013-03
Completion
2013-03

Drugs

EvaluationDrugModalityDoseRoute
Subject LCZ696 Unknown 100 mg
Subject LCZ696 Unknown 200 mg
Subject LCZ696 Unknown 400 mg