drugset / Trial / NCT01370499
A Study of LY2216684 in Participants With Major Depression Disorder
NaSingle-groupOpen-labelTreatment
Summary
The primary objective of this study is to evaluate the long-term safety and tolerability of LY2216684 administered once daily in the adjunctive treatment with an Selective Serotonin Reuptake Inhibitors (SSRI) for up to approximately 1 year in participants with Major Depressive Disorder (MDD) who were partial responders to their SSRI treatment.
Timeline
- Start
- 2011-08
- Primary completion
- 2014-01
- Completion
- 2014-01
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | edivoxetine | Small molecule | 12 mg | Oral |
| Subject | edivoxetine | Small molecule | 18 mg | Oral |