drugset / Trial / NCT00389779

DORADO-AC - Optimized Doses of Darusentan as Compared to an Active Control in Resistant Hypertension

NCT00389779

Phase 3 Completed 849 enrolled Gilead Sciences
RandomizedParallel-groupQuadruple-blindTreatment

Summary

This is a randomized, double-blind, placebo- and active-controlled study of a new experimental drug called darusentan. Darusentan is not currently approved by the United States Food and Drug Administration (FDA), which means that a doctor cannot prescribe this drug. The purpose of this study is to determine if darusentan is effective in reducing systolic and diastolic hypertension despite treatment with full doses of three or more antihypertensive drugs, including a diuretic. Subjects will be randomized to darusentan (optimized dose), an active comparator, or placebo, administered orally. The treatment period for this trial is 14 weeks.

Timeline

Start
2006-09
Primary completion
2009-08
Completion
2009-08

Drugs

EvaluationDrugModalityDoseRoute
Subject Darusentan Other / unclassified 50 mg Oral
Subject Darusentan Other / unclassified 100 mg Oral
Subject Darusentan Other / unclassified 300 mg Oral
Comparator Guanfacine Small molecule 1 mg Oral

Indications