Table 5

Summary of the PBPK models published for transporter substrates, inhibitors and inducers

Compound Modeled (Relevant Transporter)ApplicationMinimal or FullOral or IVClearanceaSimulated genotype specified?Population matched?bVerificationcAcceptance CriteriadSoftwareCitation
Inducers
Rifampin (P-gP)TransportMinimalOralBCNoA,SA, E1Simcyp(Neuhoff et al., 2013b)
Inhibitors
Cyclosporine ( OATP1B1)TransportFullOralIn vivoYesN.S.A, E1Simcyp(Varma et al., 2012)
Cyclosporine (OATP1B1, OATP1B3 BCRP)TransportFullOralBCNoAge, sex, PGXB1Simcyp(Jamei et al., 2014)
Cyclosporine (OATP1B1, OATP1B3 BCRP)DDIFullBothPENoN.S.C, E5Matlab(Gertz et al., 2013)
Gemfibrozil ( OATP1B1)DDIMinimalOralPENoN.S.A, B, E1Napp(Kudo et al., 2013)
Gemfibrozil (OATP1B1)TransportFullOralBCYesN.S.E1Simcyp(Varma et al., 2015a)* updated Varma et al 2012
Probenecid (OAT1, OAT3)DDIFullBothBCNoN.S.C1Simcyp(Hsu et al., 2014)
Verapamil (P-gp)DDIFullOralBCNoAge, sexA, E1Simcyp(Neuhoff et al., 2013b)
Substrates
Atorvastatin (OATP1B1)AbsorptionFullOralIn vitroNoAge, sexD1Simcyp(Darwich et al., 2013)
Bosentan (OATP1B1)TransportFullIVIn vitro, SFNoN.S.None1Berkeley Madonna(Jones et al., 2012)
Dabigatran (P-gp)DDIFullBothIn vitroNoN.S.A, B, E1PK Sim(Zhao and Hu, 2014)
Digoxin (P-gp)TransportFullBothBCNoAge, sexA, B4Simcyp(Neuhoff et al., 2013b)
Fluvastatin (OATP1B1)TransportFullIVIn vitro, SFNoN.S.None1Berkeley Madonna(Jones et al., 2012)
Glyburide (OATP1B1)DDIFullBothIn vitroYesPDXB, C, E1Simcyp(Varma et al., 2014)
Glyburide (OATP1B1)PregnancyFullOralBCNosexB, D, E2Simcyp, Matlab(Ke et al., 2013a)
Pravastatin (OATP1B1, OAT3)Clinical PKFullBothIn vitro, SFNoN.S.C1Matlab, PK Sim(Meyer et al., 2012)
Pravastatin (OATP1B1)TransportFullBothIn vitro, SFNoN.S.A, B, E1Simcyp(Varma et al., 2012)
Repaglinide (OATP1B1)TransportFullIVIn vitro, SFNoN.S.None1Berkeley Madonna(Jones et al., 2012)
Repaglinide (OATP1B1)RIFullOralBCYesN.S.D1Simcyp(Zhao et al., 2012a)
Repaglinide (OATP1B1)DDIMinimalOralIn vivoNoN.S.E1Napp(Kudo et al., 2013)
Repaglinide (OATP1B1)DDIFullBothBCNoN.S.C, E1Simcyp(Varma et al., 2013)
Rosuvastatin (BCRP OATP1B1, OATP1B3)TransportFullOralBC, PE, SANoAge, sexB, E1Simcyp(Jamei et al., 2014)
Rosuvastatin (OATP1B1, OATP1B3)TransportFullBothIn vitro, SFNoN.S.C1ASCLX(Bosgra et al., 2014)
Telmisartan (OATP1B3)TransportFullBothIn vitro, SFNoN.S.C1Matlab(Li et al., 2014c)
  • a BC = back calculated from in vivo data, PE = parameter estimation, SA= sensitivity analysis, SF = scaling factor.

  • b PGX = genotype, N.S. = not specified.

  • c Data sets used in model verification included: (A) Single dose PK, (B) alternative dosing regimen, (C) alternative formulation, (D) alternative population, (E) DDI.

  • d Acceptance criteria fell into 5 categories: (1) Not specified, (2) Ratio of PK parameter(s) must be within 30% of observed ratio, (3) Ratio of PK parameter(s) must be within 2 fold of observed ratio, (4) PK parameters must be within 30% of observed parameters, (5) PK parameters must be within 2 fold of observed parameters.