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A multicenter, randomized, double-blind, placebo-controlled, parallelgroup, group-sequential, adaptive, Phase 3 study with open-label extension period to assess the efficacy and safety of selexipag as an addon to standard of care therapy in subjects with inoperable or persistent/recurrent after surgical and/or interventional treatment Chronic Thromboembolic Pulmonary Hypertension

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A multicenter, randomized, double-blind, placebo-controlled, parallelgroup, group-sequential, adaptive, Phase 3 study with open-label extension period to assess the efficacy and safety of selexipag as an addon to standard of care therapy in subjects with inoperable or persistent/recurrent after surgical and/or interventional treatment Chronic Thromboembolic Pulmonary Hypertension

Status: Discontinued
Phase of Trial: Phase III

Latest Information Update: 24 Jun 2024

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At a glance

  • Drugs Selexipag (Primary)
  • Indications Pulmonary hypertension
  • Focus Registrational; Therapeutic Use
  • Acronyms SELECT
  • Sponsors Actelion Pharmaceuticals

    • Most Recent Events

    • 24 May 2023 Results evaluating efficacy and safety of selexipag in chronic thromboembolic pulmonary hypertension patients were presented at the 119th International Conference of the American Thoracic Society
    • 07 Aug 2022 This trial has been competed in Netherland, according to European Clinical Trials Database record.
    • 05 Jul 2022 Status changed from recruiting to discontinued as the study did not demonstrate efficacy on the primary endpoint, PVR vs. placebo at week 20 at a planned interim analysis.

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