4.6 Article

Lurasidone as Adjunctive Therapy With Lithium or Valproate for the Treatment of Bipolar I Depression: A Randomized, Double-Blind, Placebo-Controlled Study

期刊

AMERICAN JOURNAL OF PSYCHIATRY
卷 171, 期 2, 页码 169-177

出版社

AMER PSYCHIATRIC PUBLISHING, INC
DOI: 10.1176/appi.ajp.2013.13070985

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资金

  1. Cephalon
  2. Elan
  3. NARSAD
  4. Sunovion
  5. Takeda
  6. American Foundation for Suicide Prevention
  7. AstraZeneca
  8. Benecke
  9. Cortex Congress
  10. GlaxoSmithKline
  11. Lundbeck
  12. Medwiz Healthcare
  13. Merck
  14. Pfizer
  15. Promedica
  16. Ohio Psychiatry Association
  17. Ohio State University
  18. University of Cincinnati
  19. University of Toronto
  20. Sunovion Pharmaceuticals, Inc.

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Objective: Few studies have been reported that support the efficacy of adjunctive therapy for patients with bipolar I depression who have had an insufficient response to monotherapy with mood-stabilizing agents. The authors investigated the efficacy of lurasidone, a novel anti psychotic agent, as adjunctive therapy with lithium or valproate for the treatment of bipolar I depression. Method: Patients were randomly assigned to receive 6 weeks of double-blind adjunctive treatment with lurasidone (N=183) or placebo (N=165), added to therapeutic levels of either lithium or valproate. Primary and key secondary endpoints were change from baseline to week 6 on the Montgomery-Asberg Depression Rating Scale (MADRS) and depression severity score on the Clinical Global Impressions scale for use in bipolar illness (CGI-BP), respectively. Results: Lurasidone treatment significantly reduced mean MADRS total score at week 6 compared with the placebo group (-17.1 versus -13.5; effect size=0.34). Similarly, lurasidone treatment resulted in significantly greater endpoint reduction in CGI-BP depression severity scores compared with placebo (-1.96 versus -1.51; effect size=0.36) as well as significantly greater improvement in anxiety symptoms and in patient-reported measures of quality of life and functional impairment. Discontinuation rates due to adverse events were 6.0% and 7.9% in the lurasidone and placebo groups, respectively. Adverse events most frequently reported for lurasidone were nausea, somnolence, tremor, akathisia, and insomnia. Minimal changes in weight, lipids, and measures of glycemic control were observed during treatment with lurasidone. Conclusions: In patients with bipolar I depression, treatment with lurasidone adjunctive to lithium or valproate significantly improved depressive symptoms and was generally well tolerated.

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