OBJECTIVES: I. Determine the safety and efficacy of UT-15 in patients with severe symptomatic primary pulmonary hypertension.
PROTOCOL OUTLINE: This is a randomized, double blind, placebo controlled, multicenter study. Patients are stratified according to center and etiology of disease. Patients receive conventional oral therapy plus a continuous subcutaneous infusion of either UT-15 or placebo for 12 weeks. After completing 12 weeks of treatment, patients may continue therapy with open label UT-15. Patients who received placebo cross over to receive UT-15. Completion date provided represents the completion date of the grant per OOPD records
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Los Angeles County Harbor-UCLA Medical Center
Torrance, California, United States
Rush-Presbyterian-St. Luke's Medical Center
Chicago, Illinois, United States
University of Maryland Medical System
Baltimore, Maryland, United States
Mayo Clinic
Rochester, Minnesota, United States
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Columbia University College of Physicians and Surgeons
New York, New York, United States
United Therapeutics Corporation
Research Triangle Park, North Carolina, United States
Vanderbilt University Medical Center
Nashville, Tennessee, United States