An overview of in vitro, ex vivo and in vivo models for studying the transport of drugs across intestinal barriers

Y Xu, N Shrestha, V Préat, A Beloqui - Advanced Drug Delivery Reviews, 2021 - Elsevier
Oral administration is the most commonly used route for drug delivery owing to its cost-
effectiveness, ease of administration, and high patient compliance. However, the absorption …

Clinical probes and endogenous biomarkers as substrates for transporter drug‐drug interaction evaluation: perspectives from the international transporter consortium

X Chu, M Liao, H Shen, K Yoshida… - Clinical …, 2018 - Wiley Online Library
Drug transporters can govern the absorption, distribution, metabolism, and excretion of
substrate drugs and endogenous substances. Investigations to examine their potential …

Clinical studies on drug–drug interactions involving metabolism and transport: methodology, pitfalls, and interpretation

A Tornio, AM Filppula, M Niemi… - Clinical Pharmacology …, 2019 - Wiley Online Library
Many drug–drug interactions (DDI s) are based on alterations of the plasma concentrations
of a victim drug due to another drug causing inhibition and/or induction of the metabolism or …

Phase 0/microdosing approaches: time for mainstream application in drug development?

T Burt, G Young, W Lee, H Kusuhara… - Nature Reviews Drug …, 2020 - nature.com
Phase 0 approaches—which include microdosing—evaluate subtherapeutic exposures of
new drugs in first-in-human studies known as exploratory clinical trials. Recent progress …

Drug–drug interactions with direct oral anticoagulants

KI Foerster, S Hermann, G Mikus, WE Haefeli - Clinical Pharmacokinetics, 2020 - Springer
A large body of evidence suggests that not only direct anticoagulant effects but also major
bleeding events and stroke prevention depend on plasma concentrations of direct oral …

Antifungal drugs TDM: trends and update

B Kably, M Launay, A Derobertmasure… - Therapeutic Drug …, 2022 - journals.lww.com
Purpose: The increasing burden of invasive fungal infections results in growing challenges
to antifungal (AF) therapeutic drug monitoring (TDM). This review aims to provide an …

Drug-drug interactions that alter the exposure of glucuronidated drugs: Scope, UDP-glucuronosyltransferase (UGT) enzyme selectivity, mechanisms (inhibition and …

JO Miners, TM Polasek, JA Hulin, A Rowland… - Pharmacology & …, 2023 - Elsevier
Drug-drug interactions (DDIs) arising from the perturbation of drug metabolising enzyme
activities represent both a clinical problem and a potential economic loss for the …

Drug–drug interaction potential of darolutamide: in vitro and clinical studies

C Zurth, M Koskinen, R Fricke, O Prien… - European Journal of …, 2019 - Springer
Abstract Background and Objectives Darolutamide is a novel androgen receptor (AR)
antagonist approved for the treatment of nonmetastatic castration-resistant prostate cancer …

Disease‐associated changes in drug transporters may impact the pharmacokinetics and/or toxicity of drugs: a white paper from the International Transporter …

R Evers, M Piquette‐Miller, JW Polli… - Clinical …, 2018 - Wiley Online Library
Drug transporters are critically important for the absorption, distribution, metabolism, and
excretion (ADME) of many drugs and endogenous compounds. Therefore, disruption of …

In vitro and in vivo methods to assess pharmacokinetic drug– drug interactions in drug discovery and development

C Lu, L Di - Biopharmaceutics & drug disposition, 2020 - Wiley Online Library
Drug–drug interactions (DDIs) caused by the co‐administration of multiple drugs are major
safety concerns in the clinic. Several drugs have been withdrawn from the market due to …