Trial Profile

A Single-center, Open-label, Randomized, Two-period, Two-treatment, Crossover Study in Healthy Male Subjects to Demonstrate Bioequivalence of 1600 μg Selexipag Administered as Eight Tablets of 200 μg (Reference Drug) or as Single Tablet of 1600 μg (Test Drug)

Status: Completed

Phase of Trial: Phase I

Latest Information Update: 06 Feb 2025

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At a glance

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

08 Jul 2015 Results published in the International Journal of Clinical Pharmacology and Therapeutics.
05 Aug 2014 New trial record

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