Clinical trial
Randomized, Single Oral Dose, Two-period, Two-treatment, Two-sequence Open-label, Crossover, Bioequivalence Study to Compare Selexipag 400mcg Film Coated Tablets (400 mcg Selexipag) Versus Uptravi® 400mcg Film Coated Tablets (400 mcg Selexipag), in Healthy Subjects Under Fed Conditions
NCT06932198 is registered in ClinicalTrials.gov with Humanis Saglık Anonim Sirketi as lead sponsor.
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Registry record
As filed in ClinicalTrials.gov.
- Title
- Randomized, Single Oral Dose, Two-period, Two-treatment, Two-sequence Open-label, Crossover, Bioequivalence Study to Compare Selexipag 400mcg Film Coated Tablets (400 mcg Selexipag) Versus Uptravi® 400mcg Film Coated Tablets (400 mcg Selexipag), in Healthy Subjects Under Fed Conditions
- Lead sponsor
- Humanis Saglık Anonim Sirketi
- Phase
- Phase 1
- Overall status
- Completed
- Start date
- January 9, 2025
- Completion date
- March 25, 2025
- Enrollment
- 14 (actual)
- Sites
- 1
Conditions
As the registry lists them; a condition with its own page is linked.
pulmonary arterial hypertension (pah)