drugset / Trial / NCT01469169

Inhaled Iloprost (Ventavis): Efficacy, Safety, and Pharmacokinetics (PK) Confirmation Study

NCT01469169

Phase 3 Completed 27 enrolled Bayer
NaSingle-groupOpen-labelTreatment

Summary

This study is to investigate the efficacy, safety, and Pharmacokinetics (PK) of Inhaled Iloprost (Ventavis) therapy in Japanese pulmonary arterial hypertension (PAH) patients in Main Treatment Phase (12 weeks) and to investigate the safety, tolerability, and efficacy of longterm Inhaled Iloprost (Ventavis) therapy in Japanese PAH patients in Extension Phase.

Timeline

Start
2012-06-19
Primary completion
2014-12-26
Completion
2016-12-14

Drugs

EvaluationDrugModalityDoseRoute
Subject Iloprost Other / unclassified 2.5 ug Inhaled
Subject Iloprost Other / unclassified 5 ug Inhaled