drugset / Trial / NCT00810693

A Study to Evaluate Efficacy and Safety of Oral BAY63-2521 in Patients With Pulmonary Arterial Hypertension (PAH)

NCT00810693 ↗

Phase 3 Completed 445 enrolled Bayer
RandomizedParallel-groupTriple-blindTreatment

Summary

The aim of the study is to assess the efficacy and safety of different doses of BAY63-2521 given orally for 12 weeks, in patients with symptomatic Pulmonary Arterial Hypertension (PAH).

Timeline

Start
2008-12-17
Primary completion
2012-05-14
Completion
2012-05-14

Outcome

Met primary endpoint

paper 6-minute walk distance had increased by a mean of 30 m in the 2.5 mg-maximum group and had decreased by a mean of 6 m PMID 23883378 ↗

paper (least-squares mean difference, 36 m; 95% confidence interval, 20 to 52; P<0.001). PMID 23883378 ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Riociguat Other / unclassified 1.5 mg Oral
Subject Riociguat Other / unclassified 2.5 mg Oral