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抗体药物偶联物的药代动力学分析:ado-曲妥珠单抗恩美曲妥珠单抗的案例研究

PK assays for antibody-drug conjugates: case study with ado-trastuzumab emtansine.

作者信息

Dere Randall, Yi Joo-Hee, Lei Corinna, Saad Ola M, Huang Catherine, Li Yanhong, Baudys Jakub, Kaur Surinder

机构信息

Department of Bioanalytical Sciences, Genentech, 1 DNA Way, South San Francisco, CA 94080-4990, USA.

出版信息

Bioanalysis. 2013 May;5(9):1025-40. doi: 10.4155/bio.13.72.

Abstract

BACKGROUND

Antibody-drug conjugates (ADCs) combine the characteristics of large-molecule biologics and small-molecule drugs and are heterogeneous mixtures that can biotransform in vivo, resulting in additional complexity. ADC bioanalytical strategies require novel analytical methods, as well as existing large- and small-molecule methods. Because ADCs in late-stage clinical development are relatively new, regulatory guidelines and standard industry best practices for developing strategies for bioanalytical PK assays are still being established.

RESULTS

A PK assay strategy was developed that included comprehensive novel reagent and assay characterization approaches for the ADC ado-trastuzumab emtansine (T-DM1).

CONCLUSION

The bioanalytical strategy was successfully applied to the drug development of T-DM1 and ensured that key analytes were accurately measured in support of nonclinical and clinical development.

摘要

背景

抗体药物偶联物(ADC)兼具大分子生物制剂和小分子药物的特性,是一种可在体内发生生物转化的异质混合物,这导致其更加复杂。ADC生物分析策略既需要新颖的分析方法,也需要现有的大分子和小分子分析方法。由于处于临床开发后期的ADC相对较新,用于生物分析PK测定策略开发的监管指南和标准行业最佳实践仍在制定中。

结果

开发了一种PK测定策略,其中包括针对ADCado曲妥珠单抗(ado-trastuzumab emtansine,T-DM1)的全面新颖的试剂和测定表征方法。

结论

该生物分析策略成功应用于T-DM1的药物开发,并确保了关键分析物的准确测量,以支持非临床和临床开发。

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