United Therapeutics Corporation Completes Enrollment of FREEDOM-M Trial
FREEDOM-M is a 12-week, multi-center, international, double-blind, randomized, placebo-controlled study of a sustained release oral formulation of treprostinil diethanolamine in pulmonary arterial hypertension (PAH)patients not receiving any other approved PAH therapy.
The FREEDOM-M study enrolled 349 patients, compared to a target enrollment of 315 patients. The primary endpoint of the trial is change in six-minute walk distance at Week 12 in the treatment group compared to placebo.
"We are excited to achieve this important milestone," said
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Forward-looking Statements
Statements included in this press release that are not historical in nature are "forward-looking statements" within the meaning of the Private Securities Litigation Reform Act of 1995. Forward-looking statements include, among others, our expectations on the timing of unblinding of the FREEDOM-M study and our belief that the FREEDOM-M study unblinding will bring us closer to the goal of achieving an approved oral prostacyclin therapy for PAH. These forward-looking statements are subject to certain risks and uncertainties, such as those described in our periodic reports filed with the
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