United Therapeutics Posts Data From Remodulin Induction Before Orenitram Therapy In High Blood Pressure Patients

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  • United Therapeutics Corp UTHR announced a preliminary analysis of the EXPEDITE Phase 4 16-week study of Remodulin induction followed by oral Orenitram optimization in patients with pulmonary arterial hypertension (PAH).
  • The data demonstrated that 79% of patients in the study reached the study's primary endpoint of a 12 mg total daily dose after an up to eight-week induction treatment period with Remodulin (treprostinil) injection.
  • Also See: United Therapeutics Stops Late-Stage Tyvaso Study In Lung Disease.
  • A short induction of Remodulin (treprostinil) injection allowed study subjects to reach double the typical doses of Orenitram (treprostinil) extended-release tablets than patients who did not have a Remodulin induction.
  • A previous real-world dosing analysis showed an average Orenitram dose of approximately 6 mg daily after 16 weeks without the induction protocol studied by the EXPEDITE study. 
  • In addition, scientific literature shows that higher doses of treprostinil have been associated with better outcomes for PAH patients.
  • Treatment with Orenitram, three times daily, was well tolerated, and the safety profile was consistent with previous Orenitram studies in PAH.
  • Price Action: UTHR shares traded lower by 1.37% at $228.98 on the last check Monday.
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