Lurasidone: An Atypical Antipsychotic for Schizophrenia

Author:

Risbood Vineeta1,Lee Jennifer R2,Roche-Desilets Jennifer3,Fuller Matthew A4

Affiliation:

1. Vineeta Risbood PharmD BCPP BCPS, Clinical Pharmacy Specialist, Department of Pharmacy, Kaiser Permanente of Ohio, Parma, OH. The opinions and assertions contained herein are the private views of the author and are not to be construed as reflecting the views of Ohio Permanente Medical Group or the Kaiser Foundation Health Plan.

2. Jennifer R Lee PharmD BCPP, Mental Health Clinical Pharmacy Specialist, Department of Pharmacy, Veterans Affairs Eastern Colorado Health Care System, Denver

3. Jennifer Roche-Desilets PharmD BCPP BCPS, Clinical Pharmacy Specialist, Department of Pharmacy, Louis Stokes Cleveland Veterans Affairs Medical Center, Cleveland, OH

4. Matthew A Fuller PharmD BCPP BCPS FASHP, Clinical Pharmacy Specialist, Psychiatry, Department of Pharmacy, Louis Stokes Cleveland Veterans Affairs Medical Center; Associate Clinical Professor of Psychiatry, Clinical Instructor of Psychology, Department of Medicine, Psychiatry Service, Case Western Reserve University, Cleveland; Adjunct Associate Professor of Clinical Pharmacy, University of Toledo, Toledo, OH

Abstract

OBJECTIVE: To provide a clinical overview of the antipsychotic lurasidone. DATA SOURCES: Articles were identified by searching the MEDLINE, PubMed, Cochrane Library, and EBSCO databases (through February 2012) using the key word lurasidone. The manufacturer provided information on unpublished Phase 2 and 3 trials. The Clinicaltrials.gov database was reviewed for the status of ongoing and upcoming trials. STUDY SELECTION AND DATA EXTRACTION: All clinical trials lasting longer than 3 weeks and published in the English language were selected for review. Additional documentation, including the product dossier, package insert, and poster presentations supplied by the publisher, was also evaluated. DATA SYNTHESIS: Lurasidone hydrochloride is an atypical antipsychotic that is approved for the treatment of schizophrenia. It is under investigation for treatment of bipolar I disorder. It should be administered with food, is pregnancy category B, is contraindicated for coadministration with strong CYP3A4 inducers and inhibitors, and requires dose adjustments with certain medications and in renal and hepatic impairment. Like other atypical antipsychotics, lurasidone possesses dopamine D2 and serotonin 5-HT2A antagonism but exhibits little affinity for histamine H1, α1-adrenergic, or cholinergic M1 receptors. Additionally, it is a potent 5-HT7 antagonist, which may impact depression and cognition. Phase 3 trial results revealed that 40-80 mg administered once daily resulted in statistically significant improvements in schizophrenia symptomatology compared with placebo. Lurasidone's rate of metabolic adverse events is low relative to other atypical antipsychotics; however, this is offset by dose-dependent increases in somnolence, akathisia, and parkinsonism. CONCLUSIONS: Lurasidone has shown efficacy when compared to placebo in acute schizophrenia. Full characterization of the adverse effect profile and cognitive and affective benefits requires publication of trials with longer durations.

Publisher

SAGE Publications

Subject

Pharmacology (medical)

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