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类风湿关节炎的生物治疗:迄今为止的进展。

Biological therapies for rheumatoid arthritis: progress to date.

机构信息

Department of Nuclear Medicine and Molecular Imaging, University Medical Centre Groningen, University of Groningen, The Netherlands.

出版信息

BioDrugs. 2013 Aug;27(4):329-45. doi: 10.1007/s40259-013-0021-x.

Abstract

Biologic drugs for the management of rheumatoid arthritis (RA) have revolutionized the therapeutic armamentarium with the development of several novel monoclonal antibodies, which include murine, chimeric, humanized, fully human antibodies and fusion proteins. These biologics bind to their targets with high affinity and specificity. Since 1998, nine different biologics have been approved by the US Food and Drug Administration (FDA) and European Medicines Agency (EMA) for the treatment of RA, and several others are in different stages of clinical trials. This field is in continuous evolution and new biologics are tested every year. Therefore a precise analysis is required in order to have a detailed and updated state of the art of this field. In this review, our main aim is to analyse all available biological therapies that are FDA and EMA approved for the treatment of RA and also those that are in clinical trials for the management of RA patients.

摘要

生物制剂在类风湿关节炎(RA)的治疗中具有变革性,随着几种新型单克隆抗体的发展,包括鼠源、嵌合、人源化、全人源抗体和融合蛋白。这些生物制剂与它们的靶标具有高亲和力和特异性。自 1998 年以来,美国食品和药物管理局(FDA)和欧洲药品管理局(EMA)已批准了 9 种不同的生物制剂用于治疗 RA,还有其他几种处于不同的临床试验阶段。这一领域正在不断发展,每年都有新的生物制剂进行测试。因此,需要进行精确的分析,以便对该领域的最新技术有一个详细的了解。在这篇综述中,我们的主要目的是分析所有已获得 FDA 和 EMA 批准用于治疗 RA 的生物治疗药物,以及那些正在临床试验中用于治疗 RA 患者的药物。

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