Bioanalysis of antibody–drug conjugates: American Association of Pharmaceutical Scientists Antibody–Drug Conjugate Working Group position paper

Author:

Gorovits Boris1,Alley Stephen C2,Bilic Sanela3,Booth Brian4,Kaur Surinder5,Oldfield Phillip6,Purushothama Shobha7,Rao Chetana8,Shord Stacy4,Siguenza Patricia5

Affiliation:

1. Pfizer, 1 Burtt Road, Andover, MA 01810, USA.

2. Seattle Genetics Inc, Bothell, WA, USA

3. Novartis, NJ, USA

4. US FDA, Center for Drug Evaluation & Research, MD, USA

5. Genentech, CA, USA

6. 400 Bellerive, Quebec, Canada

7. Biogen Idec Inc., MA, USA

8. Bristol-Myers Squibb, CA, USA

Abstract

Antibody–drug conjugates (ADCs) typically consist of a cytotoxic drug covalently bound to an antibody by a linker. These conjugates have the potential to substantially improve efficacy and reduce toxicity compared with cytotoxic small-molecule drugs. Since ADCs are generally complex heterogeneous mixtures of multiple species, these novel therapeutic products present unique bioanalytical challenges. The growing number of ADCs being developed across the industry suggests the need for alignment of the bioanalytical methods or approaches used to assess the multiple species and facilitate consistent interpretation of the bioanalytical data. With limited clinical data, the current strategies that can be used to provide insight into the relationship between the multiple species and the observed clinical safety and efficacy are still evolving. Considerations of the bioanalytical strategies for ADCs based on the current industry practices that take into account the complexity and heterogeneity of ADCs are discussed.

Publisher

Future Science Ltd

Subject

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

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