Article
Pharmacogenomic, pharmacokinetic, and safety analysis of CYP3A4/CYP3A5 polymorphisms of midostaurin in patients with acute myeloid leukemia.
European journal of clinical pharmacology - 23 Dec 2025
Sechaud Romain, Peters Thomas, Gu Helen, Rahmanzadeh Gholamreza, Sharma Gopal Krishna, Guichard Nathalie, Menssen Hans D
Abstract excerpt
PURPOSE: Midostaurin is predominantly metabolized by cytochrome P450 (CYP) 3A4 to form two active metabolites, CGP62221 and CGP52421. The current analysis from UNIFY, a randomized, double-blind, phase 3 study, investigated the impact of genetic polymorphism of CYP3A4/CYP3A5 on the exposure of midostaurin and its active metabolites, and on treatment-related toxicity in patients with FLT3-mutation-negative acute...
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