Loebel Antony, Xu Jane, Hsu Jay, Cucchiaro Josephine, Pikalov Andrei
Sunovion Pharmaceuticals Inc., Fort Lee, New Jersey, and Marlborough, Massachusetts.
Ann N Y Acad Sci. 2015 Nov;1358:95-104. doi: 10.1111/nyas.12965.
Bipolar disorder is a chronic, recurrent illness that ranks among the top 10 causes of disability in the developed world. As the illness progresses, major depressive episodes increasingly predominate. However, few treatment options are available that have demonstrated efficacy in the treatment of bipolar depression, either as monotherapy or adjunctive therapy in combination with mood stabilizers. Lurasidone is an atypical antipsychotic drug that was initially developed for the treatment of schizophrenia. Since no previous atypical antipsychotic development program had proceeded directly from work on schizophrenia to bipolar depression, the decision to focus on this indication represented an innovation in central nervous system drug development and was designed to address a clinically significant unmet need. The current review summarizes key results of a clinical development program undertaken to characterize the efficacy and safety of lurasidone in patients diagnosed with bipolar depression. Lurasidone is currently the only treatment for bipolar depression approved in the United States as both a monotherapy and an adjunctive therapy with lithium or valproate. The approval of lurasidone expands available treatment options for patients with bipolar depression and provides a therapy with an overall favorable risk-benefit profile.
双相情感障碍是一种慢性复发性疾病,在发达国家位列致残的十大主要病因之中。随着病情发展,重度抑郁发作越来越占主导地位。然而,无论是作为单一疗法还是与心境稳定剂联合使用的辅助疗法,在双相抑郁治疗中已证明有效的治疗选择都很少。鲁拉西酮是一种非典型抗精神病药物,最初开发用于治疗精神分裂症。由于此前没有非典型抗精神病药物研发项目直接从精神分裂症研究转向双相抑郁治疗,因此专注于这一适应症的决定代表了中枢神经系统药物研发的一项创新,旨在满足临床上一项重大的未被满足的需求。本综述总结了一项临床研发项目的关键结果,该项目旨在确定鲁拉西酮在双相抑郁患者中的疗效和安全性。鲁拉西酮目前是美国唯一获批用于双相抑郁单一疗法以及与锂盐或丙戊酸盐联合使用的辅助疗法的药物。鲁拉西酮的获批为双相抑郁患者扩大了可用的治疗选择,并提供了一种总体风险效益比良好的疗法。