drugset / Trial / NCT04288895

Open-label, Flexible-dose Study of Vortioxetine in Patients With Depression in India

NCT04288895

Phase 4 Completed 400 enrolled H. Lundbeck A/S
NaSingle-groupOpen-labelTreatment

Summary

The purpose of this study is to evaluate the safety and tolerability of flexible doses of vortioxetine (5 - 20 mg/day) over a period of 12 weeks in patients with depression in India

Timeline

Start
2020-02-20
Primary completion
2022-02-11
Completion
2022-03-12

Drugs

EvaluationDrugModalityDoseRoute
Subject Vortioxetine Unknown 5 mg Oral
Subject Vortioxetine Unknown 20 mg Oral