drugset / Trial / NCT00940680

Efficacy/Safety of Amlodipine Plus Losartan Versus Losartan in Patients With Essential Hypertension

NCT00940680 ↗

Phase 3 Completed 142 enrolled Hanmi Pharmaceutical Company Limited
RandomizedParallel-groupDouble-blindTreatment

Summary

The purpose of this study is to evaluate of efficacy and safety of amlodipine plus losartan and losartan alone in patients with essential hypertension inadequately controlled on losartan monotherapy.

Timeline

Start
2008-04
Primary completion
2008-11
Completion
2008-11

Outcome

Met primary endpoint

paper the amlodipine/losartan 5 mg/100 mg combination group achieved significantly greater reductions in SBP at week 8 PMID 22462558 ↗

paper Response rates were significantly higher in the amlodipine/losartan 5 mg/100 mg group versus the losartan 100 mg group PMID 22462558 ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject Amlodipine Other / unclassified 5 mg —
Comparator Losartan Other / unclassified 100 mg —