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Clinical Trial Summary

The purpose of this multi-center international trial is to evaluate the safety and effectiveness of adding iloprost or placebo (an inactive substance that contains no active study drug) to sildenafil therapy for pulmonary arterial hypertension (PAH). The study will also examine whether patients on sildenafil can reduce the number of iloprost inhalations from the approved 6 doses per day to 4 doses per day.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT00302211
Study type Interventional
Source Actelion
Contact
Status Terminated
Phase Phase 3
Start date February 1, 2006
Completion date July 1, 2008

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