Tyrosine Kinase Inhibitor Pharmacokinetics
From Proteopedia
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| ! Variable | ! Variable | ||
| ! 98 | ! 98 | ||
| - | ! | + | ! 30 | 
| |- | |- | ||
| ! [[Pharmacokinetics#Protein_Binding|Protein Binding]] (%) | ! [[Pharmacokinetics#Protein_Binding|Protein Binding]] (%) | ||
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| ! 99 | ! 99 | ||
| ! 95 | ! 95 | ||
| - | ! | + | ! 98 | 
| |- | |- | ||
| ! [[Pharmacokinetics#Half_Life_.28T1.2F2.29|T<sub>1/2</sub>]] (hr) | ! [[Pharmacokinetics#Half_Life_.28T1.2F2.29|T<sub>1/2</sub>]] (hr) | ||
| Line 81: | Line 81: | ||
| |- | |- | ||
| ! Metabolism | ! Metabolism | ||
| + | ! Hepatic (CYP3A4) | ||
| ! Hepatic (CYP3A4) | ! Hepatic (CYP3A4) | ||
| ! Hepatic (CYP3A4) | ! Hepatic (CYP3A4) | ||
Revision as of 08:13, 11 December 2010
| Tyrosine Kinase Inhibitor Pharmacokinetics | |||||||
|---|---|---|---|---|---|---|---|
| VEGFR & KIT Inhibitors | EGFR Inhibitors | BCR-Abl Inhibitor | |||||
| Parameter | Sunitinib (Sutent) | Sorafenib (Nexavar) | Erlotinib (Tarceva) | Gefitinib (Iressa) | Lapatinib (Tykerb) | Imatinib (Gleevec) | Nilotinib (Tasigna) | 
| Tmax (hr) | 8 | 8.3 | 2.0 | 5.4 | 4 | 3.7 | 3.0 | 
| Cmax (ng/ml) | 24.6 | 460 | 69.6 | 130 | 115 | 2070 | 411 | 
| Bioavailability (%) | Variable | 29-49 | 99 | 59 | Variable | 98 | 30 | 
| Protein Binding (%) | 95 | 99 | 93 | 90 | 99 | 95 | 98 | 
| T1/2 (hr) | 83 | 29 | 9.4 | 26.9 | 9.6 | 26.6 | 16.0 | 
| AUC (ng/ml/hr) | 1921 | 11040 | 20577 | 3850 | 1429 | 4760 | 10052 | 
| Dosage (mg) | 50 | 50 | 150 | 250 | 100 | 400 | 200 | 
| Metabolism | Hepatic (CYP3A4) | Hepatic (CYP3A4) | Hepatic (CYP3A4) | Hepatic (CYP3A4) | Hepatic (CYP3A4) | Hepatic (CYP3A4) | Hepatic (CYP3A4) | 
For Pharmacokinetic Data References, see: References
