Utility of Cytochrome P450 4F2 Genotyping to Assess Drug Interaction Risk for Brincidovovir, a Cytochrome P450 4F2 Substrate

• Published in: Clinical pharmacology in drug development Vol. 13; no. 3; pp. 288 - 296
• Main Authors: Tippin, Tim, Faison, Shamia, Schuck, Virna, Dunn, John, Naderer, Odin
• Format: Journal Article
• Language: English
• Published: United States Wiley Subscription Services, Inc 01.03.2024
• Subjects: brincidofovir; CMX001; Cytochrome; Cytochrome P-450 Enzyme System; cytochrome P450 4F2; Cytosine - analogs & derivatives; Drug Interactions; Genotype; Genotype & phenotype; Humans; Organophosphonates; rs2108622; single nucleotide polymorphisms; Smallpox; United States; United States; CMX001; rs2108622; single nucleotide polymorphisms; cytochrome P450 4F2; brincidofovir
• DOI: 10.1002/cpdd.1356
• ISSN: 2160-763X; 2160-7648

Smallpox was eradicated in 1980 but remains a biothreat due to the potential release of variola virus into the general population. Brincidofovir, the second medicine approved by the US Food and Drug Administration to treat smallpox, is metabolized by oxidative and hydrolytic pathways. The oxidative pathway is initiated by cytochrome P450 4F2 (CYP4F2), an enzyme lacking clinical probes for drug interaction studies. The aim of this work was to assess the impact of reduced activity CYP4F2 variants (rs2108622, C/T and T/T) on brincidofovir pharmacokinetics as a surrogate for drug inhibition. Genotyping was performed on blood from healthy participants receiving oral (n = 261) and intravenous (IV, n = 49) brincidofovir across 6 phase 1 trials. Plasma concentrations were measured by validated liquid chromatography tandem mass spectrometry methods. After oral administration, subjects with the lowest activity CYP4F2 genotype (T/T) had up to 36% higher AUCinf and 29% higher Cmax while subjects with the moderate activity CYP4F2 genotype (C/T) had similar Cmax and AUCinf compared to those with the wild‐type genotype. Little to no increase in brincidofovir exposure parameters was observed following IV administration. Based on the lack of significant increases in brincidofovir plasma concentrations in subjects with low activity CYP4F2, a clinically meaningful drug–drug interaction is not expected with CYP4F2 inhibitor and brincidofovir coadministration.