Clinical Trial

Bioequivalence Study of Vortioxetine in 20 mg Coated Tablets in Healthy Subjects Under Fasting Conditions

Study acronym: ACL24-PC031
Completed Phase 1
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Summary
Prospective, longitudinal, single-dose, randomized, open-label, crossover 2x2, two treatments, two periods, two sequences controlled clinical study
Trial Details
NCT Number NCT07624357
Lead Sponsor ADIUM
Conditions Bioequivalance
Enrollment 20 participants
Start Date 2025-03-18
Primary Completion 2025-05-05 (estimated)
Study Completion 2025-05-05 (estimated)
Updated on ClinicalTrials.gov 2026-06-03