drugset / Trial / NCT00696241

Efficacy and Safety of Azilsartan Medoxomil in Participants With Essential Hypertension

NCT00696241

Phase 3 Completed 1275 enrolled Takeda
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The purpose of this study is to determine the safety and efficacy of azilsartan medoxomil, once daily (QD), compared to placebo and olmesartan in participants with essential hypertension.

Timeline

Start
2007-06
Primary completion
2008-10
Completion
2008-10

Drugs

EvaluationDrugModalityDoseRoute
Subject Azilsartan medoxomil Other / unclassified 20 mg Oral
Subject Azilsartan medoxomil Other / unclassified 40 mg Oral
Subject Azilsartan medoxomil Other / unclassified 80 mg Oral
Subject Olmesartan Other / unclassified 40 mg Oral