United Therapeutics Reports the First Patient Enrollment in P-III TETON Study of Tyvaso for Idiopathic Pulmonary Fibrosis

Shots:

• The first patient has enrolled in P-III TETON study to evaluate the safety and efficacy of treprostinil (Inhalation Solution) or PBO in a ratio (1:1) in 396 adult patients with IPF
• The 1EPs of the study is the change in FVC from baseline@ 52 wks. and 2EPs include time to clinical worsening, time to first acute exacerbation, OS @ 52wks., change in percent predicted FVC from baseline & change in KBILD
• The study is designed to validate the antifibrotic effects of treprostinil in IPF patients while FDA has approved Tyvaso for both pulmonary AH & PH-ILD and has granted OD designation for IPF

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