Bioanalytical approaches for characterizing catabolism of antibody–drug conjugates

Author:

Saad Ola M1,Shen Ben-Quan2,Xu Keyang1,Khojasteh S Cyrus3,Girish Sandhya4,Kaur Surinder1

Affiliation:

1. Department of Bioanalytical Sciences, Assay Development and Technology, Genentech, Inc., 1 DNA Way, South San Francisco, CA 94080, USA

2. Department of Preclinical & Translational Pharmacokinetics & Pharmacodynamics, Genentech, Inc., 1 DNA Way, South San Francisco, CA 94080, USA

3. Department of Drug Metabolism and Pharmacokinetics, Genentech, Inc., 1 DNA Way, South San Francisco, CA 94080, USA

4. Department of Clinical Pharmacology, Genentech, Inc., Genentech, Inc., 1 DNA Way, South San Francisco, CA 94080, USA

Abstract

The in vivo stability and catabolism of antibody–drug conjugates (ADCs) directly impact their PK, efficacy and safety, and metabolites of the cytotoxic or small molecule drug component of an ADC can further complicate these factors. This perspective highlights the importance of understanding ADC catabolism and the associated bioanalytical challenges. We evaluated different bioanalytical approaches to qualitatively and quantitatively characterize ADC catabolites. Here we review and discuss the rationale and experimental strategies used to design bioanalytical assays for characterization of ADC catabolism and supporting ADME studies during ADC clinical development. This review covers both large and small molecule approaches, and uses examples from Kadcyla® (T-DM1) and a THIOMAB™ antibody–drug conjugate to illustrate the process.

Publisher

Future Science Ltd

Subject

Medical Laboratory Technology,Clinical Biochemistry,General Pharmacology, Toxicology and Pharmaceutics,General Medicine,Analytical Chemistry

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