Geneva, Oct. 21 -- International Clinical Trials Registry received information related to the study (NCT07204314) titled 'A Study of Vortioxetine in Japanese Pediatric Patients With Major Depressive Disorder' on Sept. 30.
Study Type: Interventional
Study Design:
Allocation: Randomized. Intervention model: Parallel Assignment. Primary purpose: Treatment. Masking: Triple (Participant, Care Provider, Investigator).
Primary Sponsor: Takeda
Condition:
Major Depressive Disorder
Intervention:
Drug: Vortioxetine tablets
Recruitment Status: Not recruiting
Phase: Phase 3
Date of First Enrollment: October 1, 2025
Target Sample Size: 180
To know more, visit https://clinicaltrials.gov/study/NCT07204314
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