Pulmonary Arterial Hypertension Clinical Trial
Official title:
A Phase 2a, Double-Blind, Placebo-Controlled Multicenter Study to Assess the Safety, Tolerability, Pharmacokinetics and Pharmacodynamic Effects of RVT-1201 in Patients With Pulmonary Arterial Hypertension
This is an exploratory Phase 2a, randomized, double-blind, placebo-controlled, parallel-group, multicenter study to evaluate the safety, tolerability, pharmacokinetics, and pharmacodynamic effects of RVT-1201 in patients with pulmonary arterial hypertension (PAH).
This is an exploratory Phase 2a, randomized, double-blind, placebo-controlled,
parallel-group, multicenter study to evaluate the safety, tolerability, pharmacokinetics, and
pharmacodynamic effects of RVT-1201 in patients with pulmonary arterial hypertension (PAH).
Study participation for each patient will last approximately 3 months and will consist of a
screening period (up to 28 days in duration), a baseline period (day 1, pre-dose), a 6-week
treatment period, and a 2-week follow-up period.
The study will enroll approximately 36 patients at approximately 20 centers across the United
States and Canada.
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