Clinical trial

Inhaled Iloprost in Adults With Abnormal Pulmonary Pressure and Associated With…

NCT00109681 · Actelion, Industry · Completed

Key facts

NCT number NCT00109681
Title Inhaled Iloprost in Adults With Abnormal Pulmonary Pressure and Associated With Idiopathic Pulmonary Fibrosis
Official title A Randomized, Double-blind, Placebo-Controlled Phase II Study to Evaluate the Safety and Pilot Efficacy of Iloprost Inhalation Solution in Adults With Abnormal Pulmonary Arterial Pressure and Exercise Limitation Associated With Idiopathic Pulmonary Fibrosis (IPF)
Lead sponsor Actelion, Industry
Status Completed
Phase Phase 2
Study type Interventional
Conditions Pulmonary Fibrosis, Pulmonary Hypertension
Intervention type Drug
Interventions Iloprost Inhalation Solution (Ventavis)
Enrollment 50
Start date Apr 1, 2005
Primary completion Oct 1, 2006
Completion Oct 1, 2006
First posted May 3, 2005
Last update posted Feb 15, 2010
Countries United States

At a glance

  • 10–99 Study sites
  • No Results posted
  • None Linked FDA submissions

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

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Source: U.S. National Library of Medicine (NLM), ClinicalTrials.gov · Source date:

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