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NCT07624357
Clinical Trial
Bioequivalence Study of Vortioxetine in 20 mg Coated Tablets in Healthy Subjects Under Fasting Conditions
Study acronym:
ACL24-PC031
Completed
Phase 1
View on ClinicalTrials.gov →
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