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Research ArticleArticle

Risk of Clinically Relevant Pharmacokinetic-based Drug-drug Interactions with Drugs Approved by the U.S. Food and Drug Administration Between 2013 and 2016

Jingjing Yu, Zhu Zhou, Jessica Tay-Sontheimer, Rene H. Levy and Isabelle Ragueneau-Majlessi
Drug Metabolism and Disposition March 23, 2018, dmd.117.078691; DOI: https://doi.org/10.1124/dmd.117.078691
Jingjing Yu
1 University of Washington;
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  • For correspondence: imaj@uw.edu jingyu@uw.edu
Zhu Zhou
2 University of the Pacific
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Jessica Tay-Sontheimer
1 University of Washington;
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Rene H. Levy
1 University of Washington;
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Isabelle Ragueneau-Majlessi
1 University of Washington;
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  • For correspondence: imaj@uw.edu jingyu@uw.edu

Data Supplement

  • Supplemental Data -

    Supplemental Table 1 - NDAs approved by the U.S. FDA from 2013 to 2016
    Supplemental Table 2 - Chemical structures of compounds within the NDAs approved in 2016 (ordered by approval date)
    Supplemental Table 3 -  Inhibition DDIs, NME as substrate
    Supplemental Table 4 - Induction DDIs, NME as substrate
    Supplemental Table 5 - Inhibition DDIs, NME as inhibitor
    Supplemental Table 6 - Induction DDIs, NMEs as inducers
    Supplemental Figure 1A - Therapeutic classes for inhibition DDIs with AUC ratios ≥ 5, NME as substrate (N = 14)
    Supplemental Figure 2A - Therapeutic classes for induction DDIs with AUC ratios ≤ 0.2, NME as substrate (N = 14)
    Supplemental Figure 3A - Therapeutic classes for inhibition DDIs with 2 ≤ AUC ratios < 5, NME as inhibitor (N = 11)

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