Clinical Investigation Into Inhaled Treprostinil Sodium in Patients With Severe Pulmonary Arterial Hypertension (PAH)
Completed
United Therapeutics
Phase 3
2005-06-01
This is a double-blind placebo-controlled clinical investigation into the efficacy and
tolerability of inhaled treprostinil in patients with severe pulmonary arterial hypertension.
The primary outcome is the change in 6-minute walk distance from baseline to week 12.
Safety Evaluation of Inhaled Treprostinil Administration Following Transition From Inhaled Ventavis in Pulmonary Arterial Hypertension (PAH) Subjects
Completed
United Therapeutics
Phase 4
2008-09-01
This is a 24-month, multi-center, prospective, open-label, safety evaluation in PAH subjects
following transition from a stable dose of inhaled iloprost (Ventavis).
Subjects are to be evaluated for safety throughout the course of the study while secondary
assessments will be conducted at Baseline, Week 6, Week 12, and Months 6, 12, 18 and 24
following initiation of treprostinil sodium.
Study of Incidence of Respiratory Tract AEs in Patients Treated With Tyvaso® Compared to Other FDA Approved PAH Therapies
Completed
United Therapeutics
2010-12-01
A surveillance of respiratory tract related adverse events in patients treated with
Tyvaso®(treprostinil) Inhalation Solution versus other FDA approved therapies
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