Finding studies
Finding studies
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Lead
Takeda
This is a randomized, double-blind, placebo-controlled, parallel-group, phase III study to assess the efficacy and safety of 8-week treatment of two fixed doses of Vortioxetine (Lu AA21004; 10 or 20 mg/day) in Japanese participants with major depressive disorder (MDD).
Age
20–75
Sex
ALL
Healthy volunteers
Not accepted