CI

At a glance

ClinicalIndex Comparison Record
Phase 3Completed· 266 enrolled
Drug / intervention
LCZ696 +2 moredrug
Likely dose
LCZ696 200mgfrom record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT01663233
NCT01663233Phase 3Completed

A Randomized, 8-week, Double-blind, Parallel-group, Active-controlled, Multicenter Study to Evaluate the Efficacy and Safety of the Combination of LCZ696 200 mg + Amlodipine 5 mg in Comparison With Amlodipine 5 mg in Patients With Essential Hypertension Not Adequately Responsive to Amlodipine 5 mg Monotherapy Treatment

Novartis Pharmaceuticals·interventional·Posted Aug 13, 2012·Updated Oct 23, 2015

In Brief

A Phase 3 clinical trial evaluating LCZ696, Amlodipine, and 1 other intervention for Essential Hypertension. Completed, enrolled 266 participants across 28 sites in 6 countries.

Detailed Summary

This study will assess whether LCZ696 when used in combination with amlodipine will provide greater BP lowering benefit compared to amlodipine alone in Asian hypertensive patients not adequately responsive to amlodipine therapy.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesChina, Japan, Malaysia, Philippines, South Korea, Taiwan
Collaborators--

Timeline

Phase 3CompletedFinished
20132014201520162017201820192020202120222023202420252026
First PostedAug 13, 2012
Enrollment StartAug 1, 2012
Primary CompletionMay 1, 2013
TodayJul 2, 2026
Enrollment to primary: 9 monthsPosted 13.9 years ago

Interventions

LCZ696drug

LCZ696 will use tablets available at a strength of 200mg. Patients will be instructed to take the prescribed medication once a day.

Amlodipinedrug

Amlodipine will use tablets available at a strength of 5 mg. Patients will be instructed to take the prescribed medication once a day.

Placebodrug

Matching placebo to LCZ696