Major Depressive Disorder (MDD Clinical Trial
Official title:
Single Dose Study to Evaluate Dose-proportionality of Vortioxetine Hemihydrobromide Orally Disintegrating Tablets (5 mg, 10 mg and 20 mg) in Healthy Adult Human Subjects Under Fasting Conditions
An open label, randomized, three-period, three-treatment, six-sequence, crossover, balanced, single dose, dose proportionality study.
Single dose study to evaluate dose-proportionality of Vortioxetine Hemihydrobromide Orally Disintegrating Tablets (5 mg, 10 mg and 20 mg) in healthy adult human subjects under fasting conditions. - To evaluate dose proportionality of Vortioxetine Hemihydrobromide Orally Disintegrating Tablets (5 mg, 10 mg and 20 mg) in healthy, adult, human subjects under fasting conditions. - To monitor the safety and tolerability of the subjects. An open label, randomized, three-period, three-treatment, six-sequence, crossover, balanced, single dose, dose proportionality study. ;