drugset / Trial / NCT01085812

Relapse-Prevention Study With Levomilnacipran ER (F2695 SR) in Patients With Major Depressive Disorder

NCT01085812

Phase 3 Completed 734 enrolled Forest Laboratories
RandomizedParallel-groupTriple-blindTreatment

Summary

The purpose of this study is to evaluate the safety and efficacy of Levomilnacipran ER relative to placebo in the prevention of depression relapse in patients with major depressive disorder (MDD).

Timeline

Start
2010-03
Primary completion
2011-10
Completion
2011-10

Drugs

EvaluationDrugModalityDoseRoute
Subject Levomilnacipran Small molecule 40 mg Oral
Subject Levomilnacipran Small molecule 80 mg Oral
Subject Levomilnacipran Small molecule 120 mg Oral