Bartoli Francesco, Cavaleri Daniele, Riboldi Ilaria, Capogrosso Chiara Alessandra, Carrà Giuseppe
School of Medicine and Surgery, University of Milano-Bicocca, Monza, 20900, Italy.
Psychol Res Behav Manag. 2025 Jun 17;18:1455-1469. doi: 10.2147/PRBM.S474513. eCollection 2025.
Risperidone was the first second-generation antipsychotic to be developed as a long-acting injectable (LAI). In the early 2000s, a risperidone microsphere formulation, intramuscularly administered every 2 weeks (BW-RLAI), was introduced. To date, five different risperidone LAI formulations have been marketed - including a second biweekly microsphere injection (LY03004), a newer monthly intramuscular formulation using in situ microparticles (ISM) technology that does not require an oral risperidone run-in, and two subcutaneous formulations (RBP-7000 and TV-46000). Understanding the advantages and limitations of each option is essential for tailoring treatment regimens based on clinical needs and patient preferences. In this review, with the aim of offering insights for clinical practice and future research, we provide a comprehensive synthesis of the currently available risperidone LAI formulations, examining their efficacy and safety for the treatment of schizophrenia and bipolar I disorder. While evidence supporting the efficacy, tolerability, and safety of risperidone LAI for schizophrenia is available for all marketed formulations to date, advantages for newer formulations, such as longer dosing intervals without oral supplementation, are also reviewed. In addition, although the Food and Drug Administration approved the biweekly LAIs for bipolar I disorder, there is no data on effectiveness of the other risperidone LAI formulations for this indication so far. The variety of the available risperidone LAI options is likely to enable a more personalized treatment approach. To facilitate this, healthcare providers should develop a comprehensive understanding of these formulations to select the most suitable option. While risperidone ISM, RBP-7000, and TV-46000 may enhance treatment feasibility and adherence, further research is needed to build an evidence base comparable to that available for BW-RLAI, particularly in the treatment of BD.
利培酮是首个被开发成长效注射剂(LAI)的第二代抗精神病药物。在21世纪初,一种每2周肌肉注射一次的利培酮微球制剂(BW-RLAI)问世。迄今为止,已有五种不同的利培酮长效注射剂制剂上市,包括第二种每两周一次的微球注射剂(LY03004)、一种使用原位微粒(ISM)技术的新型每月一次肌肉注射制剂,该技术无需口服利培酮导入期,以及两种皮下注射制剂(RBP-7000和TV-46000)。了解每种选择的优缺点对于根据临床需求和患者偏好制定治疗方案至关重要。在本综述中,为了为临床实践和未来研究提供见解,我们对目前可用的利培酮长效注射剂制剂进行了全面综述,考察了它们治疗精神分裂症和双相I型障碍的疗效和安全性。虽然迄今为止所有上市制剂都有证据支持利培酮长效注射剂治疗精神分裂症的疗效、耐受性和安全性,但也对新型制剂的优势进行了综述,如无需口服补充剂即可延长给药间隔。此外,尽管美国食品药品监督管理局批准了每两周一次的长效注射剂用于双相I型障碍,但目前尚无其他利培酮长效注射剂制剂用于该适应症有效性的数据。现有多种利培酮长效注射剂选择可能会促成更个性化的治疗方法。为便于实现这一点,医疗保健提供者应全面了解这些制剂,以选择最合适的选项。虽然利培酮原位微粒制剂、RBP-7000和TV-46000可能会提高治疗的可行性和依从性,但还需要进一步研究以建立与BW-RLAI相当的证据基础,尤其是在双相障碍的治疗方面。