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Drug Evaluation

Brexpiprazole for the treatment of schizophrenia

, &
Pages 217-223 | Received 27 Aug 2016, Accepted 16 Dec 2016, Published online: 16 Jan 2017
 

ABSTRACT

Introduction: Limited efficacy on negative and cognitive symptoms and adverse effects of current antipsychotics raise the need of developing new antipsychotics. Brexpiprazole, a new antipsychotic drug approved by the U.S. Food and Drug Administration in July 2015 for the treatment of schizophrenia, is a novel serotonin-dopamine receptor modulator with partial agonist activity at serotonin 1A (5-HT1A) and D2/3 receptors.

Areas covered: We reviewed brexpiprazole related in vitro and in vivo studies, including phase II and phase III clinical trials in this article. Brexpiprazole showed significant improvement of psychotic symptoms for patients with schizophrenia in clinical trials. Most of the clinical trials demonstrated the antipsychotic effect of brexpiprazole using Positive and Negative Syndrome Scale (PANSS) in acute schizophrenia patients, and found that higher doses (2–4 mg daily) of brexpiprazole had better outcomes. In short-term trials, brexpiprazole did not show benefit for cognitive function in 6 weeks. Insomnia, akathisia, headache, and agitation were the most frequently recorded adverse events.

Expert commentary: Brexpiprazole showed better efficacy than placebo in acute phase of schizophrenia. Long-term studies are needed to investigate the efficacy of brexpiprazole for cognitive function as well as the strength and weakness of brexpiprazole among current antipsychotic drugs.

Declaration of interest

WY Hsu received the speaker bureaus from Otsuka, Johnson & Johnson, and Astellas pharmaceutical companies. HY Lane received the speaker bureaus from Otsuka, Johnson & Johnson, Eli Lily, Servier and AstraZeneca pharmaceutical companies. CH Lin received the speaker bureaus from Otsuka, Johnson & Johnson, Eli Lily, Servier and AstraZeneca pharmaceutical companies. The authors have no other relevant affiliations or financial involvement with any organization or entity with a financial interest in or financial conflict with the subject matter or materials discussed in the manuscript apart from those disclosed.

Box 1. Drug summary box.

Additional information

Funding

This paper was not funded.

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