Safety and Efficacy of Levomilnacipran ER (F2695 SR) in Major Depressive Disorder
Completed
Forest Laboratories
Phase 3
2009-09-01
The purpose of this study is to evaluate the efficacy, safety, and tolerability of
Levomilnacipran ER versus placebo in the treatment of outpatients with major depressive
disorder.
Safety and Efficacy of Levomilnacipran ER (F2695 SR) in Major Depressive Disorder
Completed
Forest Laboratories
Phase 3
2009-09-01
The purpose of this study is to evaluate the efficacy, safety, and tolerability of
Levomilnacipran ER fixed doses versus placebo in the treatment of outpatients with major
depressive disorder.
Safety and Efficacy of Levomilnacipran ER (F2695 SR) in Major Depressive Disorder
Completed
Forest Laboratories
Phase 3
2009-12-01
The purpose of this study is to evaluate the efficacy, safety, and tolerability of
Levomilnacipran ER versus placebo in the treatment of outpatients with major depressive
disorder
Relapse-Prevention Study With Levomilnacipran ER (F2695 SR) in Patients With Major Depressive Disorder
Completed
Forest Laboratories
Phase 3
2010-03-01
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).
Safety and Efficacy of Levomilnacipran ER (F2695 SR) in Adults With Fatigue Associated With Major Depressive Disorder
Completed
Forest Laboratories
Phase 2
2011-04-01
The purpose of the study is to evaluate the efficacy, safety and tolerability of
Levomilnacipran ER for the treatment of fatigue associated with major depressive disorder
(MDD).
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