Effects of Ventavis in Patients With Pulmonary Hypertension (PH) Secondary to Chronic Obstructive Pulmonary Disease (COPD)

PHASE2TerminatedINTERVENTIONAL
Enrollment

2

Participants

Timeline

Start Date

March 31, 2012

Primary Completion Date

November 30, 2012

Study Completion Date

November 30, 2012

Conditions
Chronic Obstructive Pulmonary DiseasePulmonary Hypertension
Interventions
DRUG

Iloprost

5ug dose of inhaled iloprost (20ug/mL solution) administered 6 to 9 times per day for 4 weeks

DRUG

Placebo

matching placebo

Trial Locations (11)

15213

University of Pittsburgh Medical Center, Pittsburgh

19140

Temple University Hospital, Philadelphia

32224

Mayo Clinic Jacksonville, Jacksonville

44195

Cleveland Clinic, Cleveland

54500

Hopital d'adultes de Brabois, Vandœuvre-lès-Nancy

60611

Northwestern University, Chicago

70112

Ochsner Clinic Foundation, New Orleans

73104

University of Oklahoma Health Sciences Center, Oklahoma City

90502

Los Angeles Biomedical Research Institute, Torrance

02114

Massachusetts General Hospital, Boston

08036

Hospital Clinic i Provincial, Barcelona

Sponsors

Lead Sponsor

All Listed Sponsors
lead

Actelion

INDUSTRY

NCT01437878 - Effects of Ventavis in Patients With Pulmonary Hypertension (PH) Secondary to Chronic Obstructive Pulmonary Disease (COPD) | Biotech Hunter | Biotech Hunter