Table 3.
PBPK models and model details for recognized P450 inhibitors
Enzyme Inhibited | Compound | Application | Minimal or Full PBPK | Oral or IV | Clearancea | Additional Inhibition Parameters | Simulated genotype specified? | Population matched?b | Verificationc | Acceptance Criteriad | Software | Citation |
---|---|---|---|---|---|---|---|---|---|---|---|---|
Strong Inhibitors | ||||||||||||
CYP2C8 | Gemfibrozil | DDI | Minimal | Oral | PE | CYP3A4 | No | N.S. | A, B, E | 1 | Napp | (Kudo et al., 2013) |
CYP2D6 | Paroxetine | Pregnancy | Full | Oral | In vitro | CYP3A4 | Yes | Sex, PGX | D, E | 2 | Simcyp, Matlab | (Ke et al., 2013b) |
Fluoxetine | DDI | Minimal | Oral | In vitro | CYP1A2 | Yes | N.S. | E | 1 | Simcyp | (Siccardi et al., 2013) | |
CYP2C9 | ||||||||||||
CYP2C19 | ||||||||||||
CYP3A4 | Clarithromycin | DDI | Minimal | Oral | In vivo | — | Yes | Age, Sex, PGX | A, B, E | 3 | Simcyp | (Wang, 2010) |
Clarithromycin | DDI | Minimal | Oral | In vivo | — | No | Age, Sex, PGX | B, E | 3 | Simcyp | (Xu et al., 2009) | |
Itraconazole | DDI | Minimal | Oral | PE | — | No | N.S. | A, B, E | 1 | Napp | (Kudo et al., 2013) | |
Ritonavir | DDI | Minimal | Oral | In vitro | CYP2C9 | Yes | N.S. | A, E | 1 | Simcyp | (Siccardi et al., 2013) | |
CYP2D6 | ||||||||||||
Ritonavir | Clinical PK | Minimal | Oral | In vitro | CYP3A5 | Yes | N.S. | D | 1 | Simcyp | (Kaspera et al., 2014) | |
CYP2D6 | ||||||||||||
CYP2J2 | ||||||||||||
Telithromycin | RI | Full | Oral | BC | P-gp | Yes | N.S. | D, E | 1 | Simcyp | (Zhao et al., 2012a) | |
Telithromycin | DDI | Full | Oral | BC | P-gp | No | N.S. | A, B, E | 1 | Simcyp | (Vieira et al., 2012) | |
CYP3A5 | ||||||||||||
Moderate Inhibitors | ||||||||||||
CYP2C9 | Amiodarone | DDI | Full | Both | BC | CYP2D6 | No | N.S. | A, E | 1 | Simcyp | (Chen et al., 2015) |
CYP3A4 | ||||||||||||
CYP2C19 | Omeprazole | Clinical PK | Minimal | Both | BC | — | Yes | PGX | B, D, E | 1 | Simcyp | (Wu et al., 2014) |
CYP3A4 | Diltiazem | DDI | Minimal | Oral | In vivo | — | No | Age, Sex, PGX | B, E | 3 | Simcyp | (Xu et al., 2009) |
Diltiazem | DDI | Minimal | Oral | In vitro | — | No | N.S. | A, B, E | 1 | WinNonlin | (Zhang et al., 2009) | |
Diltiazem | DDI | Minimal | Oral | In vivo | CYP2D6 | No | Age, Sex | B | 1 | Simcyp | (Friedman et al., 2011) | |
Erythromycin | DDI | Minimal | Oral | In vivo | CYP2C8 | No | Age, Sex, PGX | B, E | 3 | Simcyp | (Xu et al., 2009) | |
Verapamil | DDI | Minimal | Oral | In vitro | CYP2C8 | No | N.S. | A, B, C, E | 5 | WinNonlin | (Wang et al., 2013a) | |
OATP1B1 | ||||||||||||
Verapamil | DDI | Full | Oral | BC | — | No | Age, Sex | A, E | 1 | Simcyp | (Neuhoff et al., 2013a) | |
Verapamil | DDI | Minimal | Oral | In vivo | — | No | Age, Sex, PGX | B, E | 3 | Simcyp | (Xu et al., 2009) | |
Weak Inhibitors | ||||||||||||
CYP2C8 | Trimethoprim | DDI | Minimal | Oral | In vivo | — | Yes | N.S. | B, E | 1 | Simcyp | (Yeo et al., 2013) |
PE = parameter estimation from in vivo data, BC = back-calculated from in vivo data.
PGX = genotype, N.S. = not specified.
Data sets used in model verification included: (A) Single dose PK, (B) alternative dosing regimen, (C) alternative formulation, (D) alternative population, (E) DDI.
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.