Evaluation of functional health and well-being in patients receiving levomilnacipran ER for the treatment of major depressive disorder

J Affect Disord. 2015 Jan 1:170:230-6. doi: 10.1016/j.jad.2014.09.005. Epub 2014 Sep 10.

Abstract

Introduction: Levomilnacipran extended-release (ER) is an FDA-approved serotonin norepinephrine reuptake inhibitor (SNRI) for treating major depressive disorder (MDD). SF-36v2 Health Survey outcomes from a Phase III, randomized, double-blind, placebo-controlled study (NCT00969709) were evaluated.

Methods: Prospective and post hoc analyses of SF-36 Mental and Physical Component Summaries (MCS, PCS), and individual domains compared pooled levomilnacipran ER doses (40, 80, 120 mg/day) with placebo. Patients (18-65 years) had MDD, depressive episode ≥ 8 weeks, and Montgomery-Åsberg Depression Rating Scale total score ≥ 30. SF-36 score changes from baseline to Week 8 were analyzed using ANCOVA and the observed cases approach (Intent-to-Treat [ITT] Population). Minimally important differences (MID) evaluated clinical relevance.

Results: Baseline MCS scores reflected marked mental deficits in the ITT Population (levomilnacipran ER = 529; placebo = 175). MCS change at Week 8 was significantly greater for levomilnacipran ER than placebo (LSMD [SE] = 4.8 [1.5]; P = 0.0011); MID exceeded the 3-point threshold. Baseline PCS scores suggested minimal physical deficits; no between-group difference at Week 8 was noted. LSMD was nominally statistically significant (P < 0.05) for levomilnacipran ER versus placebo in 5 domains (General Health [2.44; P = 0.0010], Vitality [2.48; P = 0.0307], Social Functioning [3.25; P = 0.0097], Role-Emotional [3.38; P = 0.0078], Mental Health [4.34; P = 0.0005]); changes in Vitality, Social Functioning, and Mental Health exceeded MID.

Limitations: The trial was limited by short duration; analyses were post hoc and adjustments were not made for multiplicity.

Conclusion: Statistically significant and clinically meaningful improvement on the MCS and several individual domains suggest overall and dimensional improvement in health-related functioning for patients with MDD treated with levomilnacipran ER versus placebo.

Keywords: Health outcomes; Levomilnacipran ER; Major depressive disorder; SF-36; Serotonin and norepinephrine reuptake inhibitor.

Publication types

  • Clinical Trial, Phase III
  • Randomized Controlled Trial
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Adult
  • Aged
  • Antidepressive Agents / administration & dosage
  • Antidepressive Agents / adverse effects*
  • Antidepressive Agents / therapeutic use*
  • Cyclopropanes / administration & dosage
  • Cyclopropanes / adverse effects*
  • Cyclopropanes / therapeutic use*
  • Delayed-Action Preparations
  • Depressive Disorder, Major / drug therapy*
  • Depressive Disorder, Major / psychology*
  • Double-Blind Method
  • Female
  • Health Status*
  • Humans
  • Male
  • Mental Health
  • Middle Aged
  • Milnacipran
  • Prospective Studies
  • Psychiatric Status Rating Scales
  • Social Behavior
  • Treatment Outcome
  • Young Adult

Substances

  • Antidepressive Agents
  • Cyclopropanes
  • Delayed-Action Preparations
  • Milnacipran

Associated data

  • ClinicalTrials.gov/NCT00969709