drugset / Trial / NCT00458042

Transitioning To IV Remodulin From Ventavis in Patients With PAH: Safety, Efficacy and Treatment Satisfaction

NCT00458042

Phase 4 Terminated 10 enrolled United Therapeutics
Non-randomizedSingle-groupOpen-labelTreatment

Summary

The purpose of this study is to compare the effects of switching from inhaled Ventavis to intravenous Remodulin in PAH patients who are considered to be failing inhaled Ventavis therapy. This study is intended to provide information on the safe transition from Ventavis to Remodulin as well as the impact intravenous Remodulin may have on overall quality of life and treatment satisfaction compared to Ventavis.

Timeline

Start
2007-03
Primary completion
Completion
2007-11

Drugs

EvaluationDrugModalityDoseRoute
Subject Treprostinil Other / unclassified Intravenous