Tyrosine Kinase Inhibitor Pharmacokinetics
From Proteopedia
| Tyrosine Kinase Inhibitor Pharmacokinetics [1][2][3][4][5][6][7][8] | |||||
|---|---|---|---|---|---|
| VEGFR Inhibitor Pharmacokinetics [9][10][11][12][13][14][15][16] | EGFR Inhibitor Pharmacokinetics [17][18][19][20][21][22][23][24] | ||||
| Parameter | Sunitinib (Sutent) | Sorafenib (Nexavar) | Erlotinib (Tarceva) | Gefitinib (Iressa) | Lapatinib (Tykerb) |
| Tmax (hr) | 8 | 8.3 | 2.0 | 5.4 | 4 |
| Cmax (ng/ml) | 24.6 | 460 | 69.6 | 130 | 115 |
| Bioavailability (%) | Variable | 29-49 | 99 | 59 | Variable |
| Protein Binding (%) | 95 | 99 | 93 | 90 | 99 |
| T1/2 (hr) | 83 | 29 | 9.4 | 26.9 | 9.6 |
| AUC (ng/ml/hr) | 1921 | 11040 | 20577 | 3850 | 1429 |
| Dosage (mg) | 50 | 50 | 150 | 250 | 100 |
| Metabolism | Hepatic (CYP3A4) | Hepatic (CYP3A4) | Hepatic - (CYP3A4) | Hepatic - (CYP3A4) | Hepatic - (CYP3A4) |
