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阿立哌唑长循环混悬注射液:用于精神分裂症的评价。

Aripiprazole Lauroxil: A Review in Schizophrenia.

机构信息

Springer, Private Bag 65901, Mairangi Bay, Auckland, 0754, New Zealand.

出版信息

Drugs. 2017 Dec;77(18):2049-2056. doi: 10.1007/s40265-017-0848-4.

Abstract

Aripiprazole lauroxil long-acting injectable (LAI) [Aristada] is an intramuscularly administered, extended-release prodrug of aripiprazole, an established atypical antipsychotic agent that, in terms of its relative position within the class, is at the low end of the risk spectrum for metabolic side effects. In the USA, aripiprazole lauroxil LAI is indicated for the treatment of schizophrenia; approved doses of the drug can be injected once-monthly (q4w), every 6 weeks (q6w) or every 2 months (q8w). The efficacy of the 441 and 882 mg q4w dosages in the treatment of acute exacerbations of schizophrenia and as long-term maintenance therapy in stable schizophrenia has been directly demonstrated in a phase III clinical trial and extension, while the efficacy of the 662 mg q4w, 882 mg q6w and 1064 mg q8w dosing regimens has been established on the basis of pharmacokinetic bridging studies. Aripiprazole lauroxil LAI therapy was generally well tolerated, with an adverse event profile consistent with that of oral aripiprazole (with the exception of injection-site reactions), including a low propensity to cause metabolic disturbances. Thus, aripiprazole lauroxil LAI extends the treatment regimen options for patients with schizophrenia; as with other LAI formulations of antipsychotic agents, it can be particularly recommended for patients with recurrent relapses related to nonadherence to oral preparations and for those who prefer this mode of administration. Moreover, unlike aripiprazole monohydrate LAI, the only other commercially available long-acting formulation of aripiprazole, aripiprazole lauroxil LAI offers more than one dosing interval option, which may be a potential advantage in terms of tailoring therapy to the needs of individual patients.

摘要

阿立哌唑癸酸酯长效肌内注射剂(LAI)[Aristada] 是一种肌肉内给予的、延长释放的阿立哌唑前体药物,阿立哌唑是一种已确立的非典型抗精神病药物,就其在该类别中的相对位置而言,它处于代谢副作用风险谱的低端。在美国,阿立哌唑癸酸酯 LAI 被批准用于治疗精神分裂症;该药物的批准剂量可每月(q4w)、每 6 周(q6w)或每 2 个月(q8w)注射一次。在一项 III 期临床试验和扩展研究中,直接证明了 441 和 882mg q4w 剂量在治疗精神分裂症急性加重和稳定精神分裂症的长期维持治疗中的疗效,而 662mg q4w、882mg q6w 和 1064mg q8w 给药方案的疗效则基于药代动力学桥接研究得到证实。阿立哌唑癸酸酯 LAI 治疗通常具有良好的耐受性,其不良事件谱与口服阿立哌唑一致(注射部位反应除外),包括导致代谢紊乱的倾向较低。因此,阿立哌唑癸酸酯 LAI 扩展了精神分裂症患者的治疗方案选择;与其他抗精神病药物的 LAI 制剂一样,它特别推荐用于因不依从口服制剂而反复发作的患者,以及偏好这种给药方式的患者。此外,与唯一另一种市售的阿立哌唑长效制剂阿立哌唑一水合物 LAI 不同,阿立哌唑癸酸酯 LAI 提供了超过一种的给药间隔选择,这可能在根据患者的需求定制治疗方面具有潜在优势。

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