Interspecies and in vitro‐in vivo scaling for quantitative modeling of whole‐body drug pharmacokinetics in patients: Application to the anticancer drug oxaliplatin

Author:

Catozzi Simona1ORCID,Hill Roger2,Li Xiao‐Mei3,Dulong Sandrine13,Collard Elodie4,Ballesta Annabelle1

Affiliation:

1. Institut Curie, Inserm U900, MINES ParisTech, CBIO ‐ Centre for Computational Biology PSL Research University Saint‐Cloud France

2. EPSRC and MRC Centre for Doctoral Training in Mathematics for Real‐World Systems University of Warwick Coventry UK

3. UPR “Chronotherapy, Cancers and Transplantation,” Faculty of Medicine Université Paris‐Saclay Villejuif France

4. CEA, CNRS, NIMBE Université Paris‐Saclay Gif‐sur‐Yvette France

Publisher

Wiley

Subject

Pharmacology (medical),Modeling and Simulation

Reference54 articles.

1. Basic Concepts in Physiologically Based Pharmacokinetic Modeling in Drug Discovery and Development

2. Impact of Physiologically Based Pharmacokinetic Models on Regulatory Reviews and Product Labels: Frequent Utilization in the Field of Oncology

3. Scientific and regulatory evaluation of mechanistic in silico drug and disease models in drug development: Building model credibility

4. Us Food and Drug Administration (FDA).The Use of Physiologically Based Pharmacokinetic Analyses – Biopharmaceutics Applications for Oral Drug Product Development Manufacturing Changes and Controls. Tech. rep. 2020.https://www.fda.gov/regulatory‐information/search‐fda‐guidance‐documents/use‐physiologically‐based‐pharmacokinetic‐analyses‐biopharmaceutics‐applications‐oral‐drug‐product

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