drugset / Trial / NCT01155661

A Safety Study in Participants With Major Depressive Disorder

NCT01155661

Phase 3 Completed 608 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 (QD) in the adjunctive treatment with a selective serotonin reuptake inhibitor (SSRI) for up to approximately 1 year in participants with major depressive disorder (MDD) who are partial responders to their SSRI treatment.

Timeline

Start
2010-10
Primary completion
2012-12
Completion
2012-12

Drugs

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