Trials / Completed
CompletedNCT01573598
Safety and Efficacy of Vilazodone in Major Depressive Disorder
A Multicenter, Randomized, Double-Blind, Placebo-Controlled, Relapse Prevention Study With Vilazodone in Patients With Major Depressive Disorder
- Status
- Completed
- Phase
- Phase 4
- Study type
- Interventional
- Enrollment
- 1,219 (actual)
- Sponsor
- Forest Laboratories · Industry
- Sex
- All
- Age
- 18 Years – 70 Years
- Healthy volunteers
- Not accepted
Summary
Safety and Efficacy of Vilazodone in Major Depressive Disorder
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Placebo | Matching placebo given orally, once per day |
| DRUG | Vilazodone | Vilazodone, 20 mg per day, oral administration |
| DRUG | Vilazodone | Vilazodone, 40 mg once per day, oral administration |
Timeline
- Start date
- 2012-04-01
- Primary completion
- 2014-10-01
- Completion
- 2015-01-01
- First posted
- 2012-04-09
- Last updated
- 2015-05-18
Locations
75 sites across 8 countries: United States, Bulgaria, Finland, Germany, Romania, Russia, Serbia, Ukraine
Source: ClinicalTrials.gov record NCT01573598. Inclusion in this directory is not an endorsement.