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Lurasidone in Schizophrenia: New Information About Dosage and Place in Therapy

机译:精神分裂症中的卢拉西酮:有关剂量和治疗位置的新信息

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Lurasidone is a newer “atypical” or “secondgeneration” antipsychotic that has received regulatory approval in the US and Canada for the treatment of schizophrenia. Recent changes in lurasidone product labeling include an expansion of the recommended dose range from 40–80 mg/day to 40–160 mg/day, administered once-daily with food. The recommended starting dose is 40 mg/day. Initial dose titration is not required. Efficacy for the treatment of acute episodes of schizophrenia was established in five, 6-week, fixed-dose, randomized, placebo-controlled trials. Additional short-term studies in patients with schizophrenia include a 3-week, randomized, double-blind trial comparing lurasidone with ziprasidone on safety and tolerability outcomes, and a 6-week, randomized, open-label switch study. Available long-term data includes a 12-month, doubleblind safety and tolerability study comparing lurasidone with risperidone; a 6-month, openlabel extension study for one of the shortterm registration studies where patients were initially randomized to receive lurasidone, olanzapine, or placebo; and a 12-month, doubleblind extension study comparing lurasidone with quetiapine extended-release after having received lurasidone, quetiapine extendedrelease, or placebo for 6 weeks. The totality of the evidence supports the overall tolerability of lurasidone, with minimal weight gain and no clinically-meaningful alterations in glucose, lipids, or the electrocardiogram corrected QT (ECG QTc) interval. The most commonly encountered adverse events that can be observed with lurasidone are somnolence, akathisia, nausea, and parkinsonism. Additional clinical trials are underway for the use of lurasidone in patients with bipolar disorder, including major depressive episodes in patients with bipolar I disorder, and in bipolar and schizophrenia maintenance. Principal advantages over some other second-generation antipsychotics are lurasidone’s highly favorable metabolic profile and once-daily dosing regimen. Additional studies are desirable to directly compare and contrast lurasidone’s efficacy with other antipsychotic agents.
机译:卢拉西酮是一种较新的“非典型”或“第二代”抗精神病药,已在美国和加拿大获得监管部门的批准,用于治疗精神分裂症。卢拉西酮产品标签的最新变化包括建议的剂量范围从每天40–80 mg /天增加到每天40–160 mg /天,与食物一起给药。推荐的起始剂量为40毫克/天。不需要初始剂量滴定。在五,六周,固定剂量,随机,安慰剂对照试验中确定了治疗精神分裂症急性发作的疗效。在精神分裂症患者中进行的其他短期研究包括一项为期3周的随机双盲试验,该研究比较了卢拉西酮和齐拉西酮的安全性和耐受性结果,以及一项为期6周的随机开放标签转换研究。可获得的长期数据包括为期12个月的双盲安全性和耐受性研究,比较了卢拉西酮和利培酮。一项为期6个月的开放标签扩展研究,用于一项短期注册研究,在该研究中,患者最初被随机分配接受卢拉西酮,奥氮平或安慰剂;以及一项为期12个月的双盲扩展研究,在接受卢拉西酮,喹硫平缓释剂或安慰剂治疗6周后,将卢拉西酮与喹硫平缓释剂进行了比较。证据的全部支持卢拉西酮的总体耐受性,体重增加最小,并且葡萄糖,脂质或经心电图校正的QT(ECG QTc)间隔无临床意义的改变。卢拉西酮最常见的不良反应是嗜睡,静坐不全,恶心和帕金森综合症。目前正在开展其他临床试验,以在双相情感障碍患者中使用Lurasidone,包括双相I型障碍患者的严重抑郁发作以及双相情感障碍和精神分裂症的维持。与其他第二代抗精神病药相比,主要优点是卢拉西酮的代谢特性良好,并且每天一次给药方案。需要进行其他研究来直接比较和对比卢拉西酮与其他抗精神病药的疗效。

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