Physiologically-Based Pharmacokinetic-Led Guidance for Patients With Cystic Fibrosis Taking Elexacaftor-Tezacaftor-Ivacaftor With Nirmatrelvir-Ritonavir for the Treatment of COVID-19

被引:17
|
作者
Hong, Eunjin [1 ]
Almond, Lisa M. [2 ]
Chung, Peter S. [3 ,4 ]
Rao, Adupa P. [3 ,4 ]
Beringer, Paul M. [1 ,4 ]
机构
[1] Univ Southern Calif, Sch Pharm, Dept Clin Pharm, Los Angeles, CA 90007 USA
[2] Certara UK Ltd, Simcyp Div, Sheffield, S Yorkshire, England
[3] Univ Southern Calif, Keck Sch Med, Dept Med, Div Pulm & Crit Care Med, Los Angeles, CA USA
[4] Univ Southern Calif, Anton Yelchin Cyst Fibrosis Clin, Los Angeles, CA 90007 USA
关键词
DRUG-DRUG INTERACTIONS; INHIBITION;
D O I
10.1002/cpt.2585
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Cystic fibrosis transmembrane conductance regulator (CFTR) modulating therapies, including elexacaftor-tezacaftor-ivacaftor, are primarily eliminated through cytochrome P450 (CYP) 3A-mediated metabolism. This creates a therapeutic challenge to the treatment of coronavirus disease 2019 (COVID-19) with nirmatrelvir-ritonavir in people with cystic fibrosis (CF) due to the potential for significant drug-drug interactions (DDIs). However, the population with CF is more at risk of serious illness following COVID-19 infection and hence it is important to manage the DDI risk and provide treatment options. CYP3A-mediated DDI of elexacaftor-tezacaftor-ivacaftor was evaluated using a physiologically-based pharmacokinetic modeling approach. Modeling was performed incorporating physiological information and drug-dependent parameters of elexacaftor-tezacaftor-ivacaftor to predict the effect of ritonavir (the CYP3A inhibiting component of the combination) on the pharmacokinetics of elexacaftor-tezacaftor-ivacaftor. The elexacaftor-tezacaftor-ivacaftor models were verified using independent clinical pharmacokinetic and DDI data of elexacaftor-tezacaftor-ivacaftor with a range of CYP3A modulators. When ritonavir was administered on Days 1 through 5, the predicted area under the curve (AUC) ratio of ivacaftor (the most sensitive CYP3A substrate) on Day 6 was 9.31, indicating that its metabolism was strongly inhibited. Based on the predicted DDI, the dose of elexacaftor-tezacaftor-ivacaftor should be reduced when coadministered with nirmatrelvir-ritonavir to elexacaftor 200 mg-tezacaftor 100 mg-ivacaftor 150 mg on Days 1 and 5, with delayed resumption of full-dose elexacaftor-tezacaftor-ivacaftor on Day 9, considering the residual inhibitory effect of ritonavir as a mechanism-based inhibitor. The simulation predicts a regimen of elexacaftor-tezacaftor-ivacaftor administered concomitantly with nirmatrelvir-ritonavir in people with CF that will likely decrease the impact of the drug interaction.
引用
收藏
页码:1324 / 1333
页数:10
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