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对 ABP 798(一种利妥昔单抗生物类似药)开发过程中所有证据的回顾。

A review of the totality of evidence in the development of ABP 798, a rituximab biosimilar.

机构信息

St Vincent Frontier Cancer Center, Billings, MT 59102, USA.

Division of Hematology and Oncology, University of Leipzig, Leipzig, Liebigstr. 19, 04106, Germany.

出版信息

Immunotherapy. 2022 Jun;14(9):727-740. doi: 10.2217/imt-2022-0024. Epub 2022 May 11.

Abstract

ABP 798 (RIABNI™) is a biosimilar to rituximab reference product (RP), a monoclonal antibody that targets CD20. Approval of ABP 798 was based on the totality of evidence generated using a stepwise approach which began by showing that it is structurally and functionally similar to rituximab RP. This analytical assessment was followed by a demonstration of pharmacokinetic/pharmacodynamic similarity in patients with rheumatoid arthritis. Comparative clinical efficacy and safety of ABP 798 with rituximab RP was demonstrated as a final step in patients with non-Hodgkin lymphoma and in those with rheumatoid arthritis. Overall, the totality of evidence supported the conclusion that ABP 798 is highly similar to rituximab RP and provided scientific justification for extrapolation to other approved indications of rituximab RP.

摘要

ABP798(RIABNI™)是一种利妥昔单抗参照产品(RP)的生物类似药,该产品是一种针对 CD20 的单克隆抗体。ABP798 的批准基于使用逐步方法产生的整体证据,该方法首先表明它在结构和功能上与利妥昔单抗 RP 相似。在类风湿关节炎患者中进行了药代动力学/药效学相似性的证明后,接着进行了比较。在非霍奇金淋巴瘤和类风湿关节炎患者中,最后一步证明了 ABP798 与利妥昔单抗 RP 的临床疗效和安全性相当。总的来说,整体证据支持 ABP798 与利妥昔单抗 RP 高度相似的结论,并为将其推广到利妥昔单抗 RP 的其他已批准适应症提供了科学依据。

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