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Revision as of 16:29, 9 December 2010 by
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Pharmacokinetics
Pharmacokinetics
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)
Dasatinib
(Sprycel)
T
max
(hr)
8
8.3
2.0
5.4
4
3.7
3.0
1.0
C
max
(ng/ml)
24.6
460
69.6
130
115
2070
411
124
Bioavailability
(%)
Variable
29-49
99
59
Variable
98
30
20
Protein Binding
(%)
95
99
93
90
99
95
98
96
T
1/2
(hr)
83
29
9.4
26.9
9.6
26.6
16.0
3.3
AUC
(ng/ml/hr)
1921
11040
20577
3850
1429
4760
10052
461
Dosage (mg)
50
50
150
250
100
400
200
200
Metabolism
Hepatic (CYP3A4)
Hepatic (CYP3A4)
Hepatic (CYP3A4)
Hepatic (CYP3A4)
Hepatic (CYP3A4)
Hepatic (CYP3A4)
Hepatic (CYP3A4)
Hepatic (CYP3A4)
For Pharmacokinetic Data References, see:
References
Proteopedia Page Contributors and Editors
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Proteopedia Page Contributors and Editors (what is this?)
David Canner
,
Joel L. Sussman
,
Alexander Berchansky
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