A Novel Treatment Option for Schizophrenia

Jeffrey Rado, P. Janicak
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引用次数: 4

Abstract

of schizophrenia, many patients do not benefit from or tolerate currently available antipsychotics. Two emerging agents recently received FDA approval: asenapine (reviewed in our last issue) and iloperidone, the focus of this article. Iloperidone (Fanapt, Vanda Pharmaceuticals, Inc.) is a novel mixed 5-HT2a/D2 antagonist, similar to other second-generation antipsychotics (SGAs). After initially being turned down by the FDAin July 2008 because of concerns about its efficacy compared with risperidone, it was approved in May 2009 for the acute treatment of schizophrenia. The recommended dose range is 12–24 mg/d titrated over the first week to minimize the risk of orthostatic hypotension. A six-marker genotype is also provided to aid in predicting clinical response. This article reviews the mechanism of action of iloperidone, data supporting its use in schizophrenia, and its safety profile.
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一种治疗精神分裂症的新方法
对于精神分裂症,许多患者不能从目前可用的抗精神病药物中获益或耐受。两种新兴药物最近获得了FDA的批准:阿塞那平(在我们的上一期中回顾过)和伊哌啶酮,这是本文的重点。Iloperidone (Fanapt, Vanda Pharmaceuticals, Inc.)是一种新型混合5-HT2a/D2拮抗剂,类似于其他第二代抗精神病药物(SGAs)。2008年7月,由于担心其与利培酮相比的疗效,该药物最初被fda拒绝,但在2009年5月被批准用于精神分裂症的急性治疗。推荐剂量范围为12 - 24mg /d,在第一周内逐渐滴定,以尽量减少直立性低血压的风险。六标记基因型也提供了帮助预测临床反应。本文综述了伊哌啶酮的作用机制,支持其在精神分裂症中的应用的数据,以及它的安全性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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