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
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Vortioxetine | Unknown | 10 mg | Intravenous |
| Subject | Vortioxetine | Unknown | 17 mg | Intravenous |