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在抗药物抗体检测中证明生物类似药与原研药抗药物抗体结合的可比性:一种实用方法。

Demonstrating biosimilar and originator antidrug antibody binding comparability in antidrug antibody assays: a practical approach.

作者信息

Ryding Janka, Stahl Michael, Ullmann Martin

机构信息

Fresenius-Kabi (SwissBiosim), Z.I. de l'Ouriettaz, 1170 Aubonne, Switzerland.

出版信息

Bioanalysis. 2017 Sep;9(18):1395-1406. doi: 10.4155/bio-2017-0111. Epub 2017 Sep 18.

Abstract

Biosimilar drug development has brought new challenges to bioanalytical ligand-binding assays used to determine drug concentration, antidrug antibodies and neutralizing antibodies. One particular challenge is how to demonstrate that the antidrug antibody assay can adequately detect antibodies against both biosimilar and originator. In this paper, we review the current guidelines and literature for practical recommendations and present a gap analysis. Case examples of antibody binding comparability testing are presented, and the challenges and implications are discussed. Based on the lessons learned from our biosimilar assay applications, we recommend a bioanalytical comparability testing approach that is outlined and discussed.

摘要

生物类似药的研发给用于测定药物浓度、抗药抗体和中和抗体的生物分析配体结合分析带来了新的挑战。一个特别的挑战是如何证明抗药抗体分析能够充分检测出针对生物类似药和原研药的抗体。在本文中,我们回顾了当前的指南和文献以获取实际建议,并进行了差距分析。文中给出了抗体结合可比性测试的案例,并讨论了挑战和影响。基于我们在生物类似药分析应用中吸取的经验教训,我们推荐了一种生物分析可比性测试方法并进行了概述和讨论。

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