drugset / Trial / NCT01370499

A Study of LY2216684 in Participants With Major Depression Disorder

NCT01370499

Phase 3 Completed 288 enrolled Eli Lilly and Company
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

EvaluationDrugModalityDoseRoute
Subject edivoxetine Small molecule 12 mg Oral
Subject edivoxetine Small molecule 18 mg Oral