Clinical Probes and Endogenous Biomarkers as Substrates for Transporter Drug‐Drug Interaction Evaluation: Perspectives From the International Transporter Consortium
Year: 2018
Type: article
Abstract: Drug transporters can govern the absorption, distribution, metabolism, and excretion of substrate drugs and endogenous substances. Investigations to examine their potential impact to pharmacokinetic (PK) drug-drug interactions (DDIs) are an integral part of the risk assessment in drug development. To evaluate a new molecular entity as a potential perpetrator of transporters, use of well characterized and/or clinically relevant probe substrates with good selectivity and sensitivity are critical for robust clinical DDI assessment that could inform DDI management strategy in the product labeling. The availability of endogenous biomarkers to monitor transporter-mediated DDIs in early phases of clinical investigations would greatly benefit downstream clinical plans. This article reviews the state-of-the-art in transporter clinical probe drugs and emerging biomarkers, including current challenges and limitations, delineates methods and workflows to identify and validate novel endogenous biomarkers to support clinical DDI evaluations, and proposes how these probe drugs or biomarkers could be used in drug development.
DOI: 10.1002/cpt.1216
Institutions: Merck & Co., Inc., Rahway, NJ, USA (United States), Clovis Oncology (United States), Bristol-Myers Squibb (United States), Genentech, BioLineRx Ltd. (Israel), United States Food and Drug Administration, Center for Drug Evaluation and Research, University of Manchester, University of California, San Francisco, The University of Tokyo, Gilead Sciences (United States), Pfizer (United States), RIKEN Center for Sustainable Resource Science, RIKEN, GlaxoSmithKline (United States)
Language: English
Subfield: Oncology
Field: Medicine
Domain: Health Sciences
Open Access status: green
OpenAlex ID: W2896835015
