Yee Anne
a Department of Psychological Medicine, University of Malaya Center for Addiction Sciences (UMCAS), Faculty of Medicine , University of Malaya , Kuala Lumpur , Malaysia.
Expert Rev Neurother. 2016;16(2):109-22. doi: 10.1586/14737175.2016.1129901. Epub 2016 Jan 20.
Brexpiprazole (OPC-34712) is a novel serotonin-dopamine activity modulator, which has recently been approved by the U.S Food and Drug Administration for the treatment of schizophrenia. The aim of this paper is to systematically synthesize all data of the efficacy, safety and tolerability of Brexpiprazole in treating schizophrenia. The terms 'Brexpiprazole', 'OPC-34712' and 'schizophrenia' were searched. A total of 12 clinical trials with 7 available data records were found. The pooled effect size of Brexpiprazole 1 mg, 2 mg and 4 mg were all superior to placebo in terms of the change from baseline in positive and negative syndrome scale (PANSS) total score at week 6 (weighted mean difference = -3.74, p = 0.044; weighted mean difference = -5.76, p < 0.01 and weighted mean difference = -7.03, p < 0.01, respectively) when compared to that of the placebo in treating acute schizophrenia. Brexpiprazole displays a good safety and tolerability profile. The incidence of akathisia, headache, insomnia, sedation, agitation, diarrhea, weight gained, nausea, and dyspepsia are comparable to placebo.
布雷哌唑(OPC - 34712)是一种新型的5-羟色胺-多巴胺活性调节剂,最近已获美国食品药品监督管理局批准用于治疗精神分裂症。本文旨在系统综合布雷哌唑治疗精神分裂症的疗效、安全性和耐受性的所有数据。检索了“布雷哌唑”“OPC - 34712”和“精神分裂症”等术语。共找到12项临床试验,有7条可用数据记录。在治疗急性精神分裂症时,与安慰剂相比,布雷哌唑1毫克、2毫克和4毫克剂量在第6周时阳性和阴性症状量表(PANSS)总分较基线的变化方面均优于安慰剂(加权平均差分别为-3.74,p = 0.044;加权平均差为-5.76,p < 0.01;加权平均差为-7.03,p < 0.01)。布雷哌唑显示出良好的安全性和耐受性。静坐不能、头痛、失眠、镇静、激越、腹泻、体重增加、恶心和消化不良的发生率与安慰剂相当。