典型文献
Itraconazole and rifampicin,as CYP3A modulators but not P-gp modulators,affect the pharmacokinetics of almonertinib and active metabolite HAS-719 in healthy volunteers
文献摘要:
Almonertinib is a novel third-generation EGFR tyrosine kinase inhibitor.It is mainly metabolized by CYP3A in vitro,and N-desmethylated almonertinib(HAS-719)is the major active metabolite in human plasma.In this study,we investigated the effects of CYP3A inhibitor itraconazole and CYP3A inducer rifampicin on the pharmacokinetics of almonertinib and HAS-719 in 64 healthy volunteers.We found that when co-administered with itraconazole,the maximal plasma concentration(Cmax)and the plasma exposure(AUC0-t)of almonertinib were increased by 56.3%and 2.38-fold,respectively,whereas the Cmax and AUC0-t of HAS-719 were reduced by 86.8%and 71.8%,respectively.Co-administration with rifampicin reduced the Cmax and AUC0-t of almonertinib by 79.3%and 92.6%,but the AUC0-t of HAS-719 was unexpectedly decreased by 72.5%.In vitro assays showed that both almonertinib and HAS-719 were substrates of CYP3A and P-gp.Co-administration of rifampicin in Beagle dogs reduced the fecal recovery of almonertinib and HAS-719,and markedly increased the levels of metabolites derived from further metabolism of HAS-719,which was consistent with human plasma data,suggesting that although rifampicin was also a potent inducer of P-gp,the pharmacokinetic alternation of HAS-719 was mainly due to its further metabolism but not excretion changes.Moreover,we revealed that almonertinib was a moderately sensitive substrate of CYP3A in vivo.Special attention should be paid to the interaction between almonertinib and drugs or food affecting CYP3A activity in the clinical application of almonertinib.
文献关键词:
中图分类号:
作者姓名:
Lu Liu;Wei Li;Le Yang;Zi-tao Guo;Hao Xue;Ning-jie Xie;Xiao-yan Chen
作者机构:
Shanghai Institute of Materia Medica,Chinese Academy of Sciences,Shanghai 201203,China;University of Chinese Academy of Sciences,Beijing 100049,China
文献出处:
引用格式:
[1]Lu Liu;Wei Li;Le Yang;Zi-tao Guo;Hao Xue;Ning-jie Xie;Xiao-yan Chen-.Itraconazole and rifampicin,as CYP3A modulators but not P-gp modulators,affect the pharmacokinetics of almonertinib and active metabolite HAS-719 in healthy volunteers)[J].中国药理学报(英文版),2022(04):1082-1090
A类:
Itraconazole,almonertinib,Almonertinib,desmethylated,itraconazole
B类:
rifampicin,CYP3A,modulators,but,not,gp,pharmacokinetics,active,HAS,healthy,volunteers,novel,third,generation,EGFR,tyrosine,kinase,inhibitor,mainly,metabolized,by,vitro,major,human,plasma,In,this,study,investigated,effects,inducer,We,found,that,when,administered,maximal,concentration,Cmax,exposure,AUC0,were,increased,fold,respectively,whereas,reduced,Co,administration,was,unexpectedly,decreased,assays,showed,both,substrates,Beagle,dogs,fecal,recovery,markedly,levels,metabolites,derived,from,further,metabolism,which,consistent,data,suggesting,although,also,potent,alternation,due,its,excretion,changes,Moreover,revealed,moderately,sensitive,vivo,Special,attention,should,paid,interaction,between,drugs,food,affecting,activity,clinical,application
AB值:
0.408218
相似文献
机标中图分类号,由域田数据科技根据网络公开资料自动分析生成,仅供学习研究参考。