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Research ArticleArticle

Application of static models to predict midazolam clinical interactions in the presence of single or multiple HCV drugs

Yaofeng Cheng, Li Ma, Shu-Ying Chang, Griffith Humphreys and Wenying Li
Drug Metabolism and Disposition May 25, 2016, dmd.116.070409; DOI: https://doi.org/10.1124/dmd.116.070409
Yaofeng Cheng
1 Bristol-Myers Squibb;
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Li Ma
1 Bristol-Myers Squibb;
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Shu-Ying Chang
1 Bristol-Myers Squibb;
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Griffith Humphreys
2 Bristol-Myers Squibb PRI
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Wenying Li
1 Bristol-Myers Squibb;
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  • For correspondence: wenying.li@bms.com

Data Supplement

Files in this Data Supplement:

  • Supplemental Data -

    Methods

    Supplement Figure 1 - Inhibition of CYP3A4 catalyzed midazolam 1'-hydroxylation by HCV compounds

    Supplement Figure 2 - Time dependent inhibition of CYP3A4 catalyzed midazolam 1'-hydroxylation by ASV (each point represents mean of triplicate, error bar represents standard deviation)

    Supplement Table 1 - Kinetic parameters of CYP3A4 inhibition and TDI by ASV, DCV, BCV and BCV-M1 in human liver microsomes

    Supplement Table 2 - Fitting outcomes for the CYP3A4 induction data

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