The effect of itraconazole, a strong CYP3A4 inhibitor, on the pharmacokinetics of the first‐in‐class ACKR3/CXCR7 antagonist, ACT‐1004‐1239

Cytochrome P450 (CYP) 3A4 is an enzyme involved in the metabolism of many drugs that are currently on the market and is therefore a key player in drug–drug interactions (DDIs). ACT‐1004‐1239 is a potent and selective, first‐in‐class ACKR3/CXRC7 antagonist being developed as a treatment for demyelina...

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Vydané v:	Clinical and translational science Ročník 17; číslo 7; s. e13883 - n/a
Hlavní autori:	Huynh, Christine, Dingemanse, Jasper, Meyer zu Schwabedissen, Henriette E., Fonseca, Marlene, Sidharta, Patricia N.
Médium:	Journal Article
Jazyk:	English
Vydavateľské údaje:	United States John Wiley & Sons, Inc 01.07.2024 John Wiley and Sons Inc Wiley
Predmet:	Adult Antifungal agents Area Under Curve Blood pressure Chemokines Cytochrome Cytochrome P-450 CYP3A - metabolism Cytochrome P-450 CYP3A Inhibitors - administration & dosage Cytochrome P-450 CYP3A Inhibitors - pharmacokinetics Cytochrome P-450 CYP3A Inhibitors - pharmacology Cytochrome P450 Demyelinating diseases Demyelination Drug dosages Drug interaction Drug Interactions Drug metabolism Enzymes Healthy Volunteers Humans Itraconazole Itraconazole - administration & dosage Itraconazole - pharmacokinetics Itraconazole - pharmacology Ligands Male Metabolism Metabolites Middle Aged Multiple sclerosis Pharmaceuticals Pharmacokinetics Young Adult Portugal
ISSN:	1752-8054, 1752-8062, 1752-8062
On-line prístup:	Získať plný text
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