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Single-center, Open-label, Phase 1 Study Consisting of a Single-dose Pilot Phase and a Randomized, Two-way Crossover, Single-dose Main Phase to Investigate the Absolute Bioavailability of a Single Oral Dose of Selexipag in Healthy Male Subjects

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Trial Profile

Single-center, Open-label, Phase 1 Study Consisting of a Single-dose Pilot Phase and a Randomized, Two-way Crossover, Single-dose Main Phase to Investigate the Absolute Bioavailability of a Single Oral Dose of Selexipag in Healthy Male Subjects

Status: Completed
Phase of Trial: Phase I

Latest Information Update: 17 Feb 2017

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At a glance

  • Drugs Selexipag (Primary) ; Selexipag (Primary)
  • Indications Arteriosclerosis obliterans; Pulmonary arterial hypertension; Pulmonary hypertension; Raynaud's disease
  • Focus Pharmacokinetics
  • Sponsors Actelion Pharmaceuticals

    • Most Recent Events

    • 24 Nov 2016 Results assessing bioavailability of oral (tablet) versus intravenous (i.v.) formulation of selexipag in healthy subjects published in the European Journal of Clinical Pharmacology.
    • 12 Sep 2016 New trial record

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