drugset / Trial / NCT00578786

A Long Term Study of Ambrisentan in Pulmonary Arterial Hypertension Subjects Having Completed AMB-320 (NCT00423748) or AMB-321 (NCT00423202)

NCT00578786

Phase 3 Completed 383 enrolled Gilead Sciences
RandomizedParallel-groupTriple-blindTreatment

Summary

AMB-320/321-E was designed to provide long-term, controlled monitoring of pulmonary arterial hypertension (PAH) patients treated with ambrisentan (AMB) in order to properly define the adverse event profile associated with this endothelin receptor antagonist (ERA), including the incidence and severity of elevated serum liver function tests (LFTs). In addition, this study continued the efficacy assessments of the previous studies, examined long-term AMB treatment success, and compared long-term survival of subjects treated with AMB to the NIH registry of patients with PAH.

Timeline

Start
2004-02
Primary completion
2010-03
Completion
2010-03

Drugs

EvaluationDrugModalityDoseRoute
Subject Ambrisentan Small molecule 2.5 mg Oral
Subject Ambrisentan Small molecule 5 mg Oral
Subject Ambrisentan Small molecule 10 mg Oral