drugset / Trial / NCT02919501

Study of the Efficacy and Safety of Initial Administration of 17 mg Vortioxetine Intravenously With 10 mg/Day Vortioxetine Orally in Patients With Major Depressive Disorder

NCT02919501

Phase 2 Completed 55 enrolled H. Lundbeck A/S Takeda · collab
RandomizedParallel-groupDouble-blindTreatment

Summary

To evaluate the early onset of efficacy of vortioxetine 17 mg intravenously (IV) and vortioxetine 10 mg/day oral dose regimen versus placebo IV and vortioxetine 10 mg/day oral dose regimen on depressive symptoms

Timeline

Start
2016-09-27
Primary completion
2017-04-27
Completion
2017-04-27

Drugs

EvaluationDrugModalityDoseRoute
Subject Vortioxetine Unknown 10 mg Intravenous
Subject Vortioxetine Unknown 17 mg Intravenous