ADME and DMPK considerations for the discovery and development of antibody drug conjugates (ADCs)
Author:
Affiliation:
1. Drug Metabolism and Pharmacokinetics, Early Oncology Research and Development, Cambridge, UK
2. Drug Metabolism and Pharmacokinetics, Early Oncology Research and Development, AstraZeneca, Boston, MA, USA
Publisher
Informa UK Limited
Subject
Health, Toxicology and Mutagenesis,Pharmacology,Toxicology,Biochemistry,General Medicine
Link
https://www.tandfonline.com/doi/pdf/10.1080/00498254.2022.2141667
Reference92 articles.
1. A Mechanistic Pharmacokinetic Model Elucidating the Disposition of Trastuzumab Emtansine (T-DM1), an Antibody–Drug Conjugate (ADC) for Treatment of Metastatic Breast Cancer
2. Conjugation site modulates the in vivo stability and therapeutic activity of antibody-drug conjugates
3. Use of translational modeling and simulation for quantitative comparison of PF-06804103, a new generation HER2 ADC, with Trastuzumab-DM1
4. Current possibilities of liquid chromatography for the characterization of antibody-drug conjugates
5. Sacituzumab Govitecan (IMMU-132), an Anti-Trop-2/SN-38 Antibody–Drug Conjugate: Characterization and Efficacy in Pancreatic, Gastric, and Other Cancers
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2. Bioanalytical Approaches to Support the Development of Antibody-Oligonucleotide Conjugate (AOC) Therapeutic Proteins;Xenobiotica;2024-04-12
3. Towards a platform quantitative systems pharmacology (QSP) model for preclinical to clinical translation of antibody drug conjugates (ADCs);Journal of Pharmacokinetics and Pharmacodynamics;2023-10-03
4. Antibody-drug conjugates in breast cancer: overcoming resistance and boosting immune response;Journal of Clinical Investigation;2023-09-15
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