drugset / Trial / NCT01193101

Efficacy and Safety of LCZ696 Compared to Placebo in Patients With Essential Hypertension

NCT01193101 ↗

Phase 2 Completed 389 enrolled Novartis Pharmaceuticals
RandomizedParallel-groupDouble-blindTreatment

Summary

This study is a phase 2 study in patients with essential hypertension.

Timeline

Start
2010-08
Primary completion
2011-04
Completion
2011-04

Outcome

Met primary endpoint

paper Reductions in clinic systolic BP, diastolic BP (P<0.0001), and pulse pressure (P<0.001) were significantly greater with all doses of LCZ696 than with placebo. PMID 24446062 ↗

Drugs

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