drugset / Trial / NCT01323478

Open-label Safety Extension Study of 15 and 20 mg of Vortioxetine (Lu AA21004) in Long-term Treatment of Major Depressive Disorder in Adults

NCT01323478

Phase 3 Completed 71 enrolled H. Lundbeck A/S
NaSingle-groupOpen-labelTreatment

Summary

To evaluate the long-term safety and tolerability of flexible doses, 15 and 20 mg/day, of Vortioxetine over a period of 52 weeks in patients with Major Depressive Disorder (MDD)

Timeline

Start
2011-04
Primary completion
2012-09
Completion
2012-10

Drugs

EvaluationDrugModalityDoseRoute
Subject Vortioxetine Unknown 15 mg Oral
Subject Vortioxetine Unknown 20 mg Oral