Pharmacokinetics of asundexian with combined CYP3A and P-gp inhibitors and an inducer: Target in vitro and in vivo studies.
Friederike KanefendtChristine BraseNatalia JungmannRobert FrickeAnna EngelenSebastian SchmitzPublished in: British journal of clinical pharmacology (2023)
The presented studies confirmed that CYP3A4 and P-gp contribute to asundexian metabolism and excretion. Observed effects were in line with data from a previous mass balance study.