Placebo Controlled Trial of Bosentan in Scleroderma Patients

PHASE2TerminatedINTERVENTIONAL
Enrollment

5

Participants

Timeline

Start Date

September 30, 2006

Primary Completion Date

September 30, 2009

Study Completion Date

March 31, 2010

Conditions
Systemic SclerodermaPulmonary Hypertension
Interventions
DRUG

Bosentan

62.5 mg by mouth (PO) twice daily (Bid) for 1 month, followed by 125 mg PO Bid thereafter, for a total of 16 weeks

DRUG

Placebo

62.5 mg PO Bid for 1 month, followed by 125 mg PO Bid thereafter, for a total of 16 weeks

Trial Locations (2)

20007

Georgetown University Medical Center, Washington D.C.

06030

University of Connecticut, Farmington

Sponsors

Collaborators (1)

All Listed Sponsors
collaborator

Actelion

INDUSTRY

lead

Georgetown University

OTHER