Sorafenib: Difference between revisions

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===Pharmacokinetics===
===Pharmacokinetics===
 
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!  colspan="6" align="center"| VEGFR Inhibitor [[Pharmacokinetics]] <ref>D. Smith et al. Br J Clin Pharmacol. 2009 April; 67(4): 421–426.</ref><ref>R. Khosravan, et al. General Poster Session, Developmental Therapeutics: Cytotoxic Chemotherapy, J Clin Oncol 26: 2008 (May 20 suppl; abstr 2578)</ref><ref>PMID:16133532</ref><ref>PMID:20821331</ref><ref>PMID:20717111</ref>
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{{:Tyrosine Kinase Inhibitor Pharmacokinetics}}
! Parameter
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! [[Sunitinib]] (Sutent)
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! [[Sorafenib]] (Nexavar)
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! [[Pharmacokinetics#Tmax|T<sub>max</sub>]] (hr)
! 8
! 8.3
|-
! [[Pharmacokinetics#Cmax|C<sub>max</sub>]] (ng/ml)
! 24.6
! 460
|-
! [[Pharmacokinetics#Bioavailability_.28F.29|Bioavailability]] (%)
! Variable
! 29-49
|-
! [[Pharmacokinetics#Protein_Binding|Protein Binding]] (%)
! 95
! 99
|-
! [[Pharmacokinetics#Half_Life_.28T1.2F2.29|T<sub>1/2</sub>]] (hr)
! 83
! 29
|-
! [[Pharmacokinetics#Area_Under_the_Curve_.28AUC.29|AUC]] (ng/ml/hr)
! 1921
! 11040
|-
! Dosage (mg)
! 50
! 50
|-
! Metabolism
! Hepatic (CYP3A4)
! Hepatic (CYP3A4)
|}