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. 2015 May 22;79(6):946–958. doi: 10.1111/bcp.12563

Figure 1.

Figure 1

Observed vs. predicted AUCR for oncology drugs as perpetrators of CYP3A DDI using the mechanistic static model for liver and intestine (A) and liver only (B). AUCR threshold of 0.8 and 1.25 shown as dotted lines as well as line of unity and 2-fold error lines