Gefitinib, also known as Iressa

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Better Known as: Iressa

  • Marketed By: AstraZeneca & Teva
  • Major Indication: Pancreatic & Small Cel Lung Cancer
  • Drug Class: EGFR Inhibitor
  • Date of FDA Approval (Expiration): 2003 (2013)
  • 2009 Sales: $268 Million
  • Importance: It is the first selective inhibitor of Epidermal Growth Factor Receptors approved by the FDA
  • The following is a list of Pharmacokinetic Parameters. See: Pharmaceutical Drugs for more information

Pharmacokinetics

EGFR Inhibitor Pharmacokinetics Comparison at Equivalent Dosages [1][2][3]
Parameter Erlotinib (Tarceva) Gefitinib (Iressa) Lapatinib (Tykerb)
Tmax (hr) 2.0 5.4 4
Cmax (ng/ml) 69.6 130 115
Bioavailability (%) 99 59 Lapatinib (Tykerb)
Protein Binding (%) 93 90 99
T1/2 (hr) 9.4 26.9 9.6
AUC (ng/ml/hr) 20577 3850 1429
Typical Dosage (mg) 150 250 100
Metabolism Hepatic - (CYP3A4, CYP3A5, CYP2D6, CYP1A1) Hepatic - (CYP3A4, CYP3A5, CYP2D6, CYP1A1, CYP1A2) Hepatic (CYP3A4)

References

  1. Hamilton M, Wolf JL, Rusk J, Beard SE, Clark GM, Witt K, Cagnoni PJ. Effects of smoking on the pharmacokinetics of erlotinib. Clin Cancer Res. 2006 Apr 1;12(7 Pt 1):2166-71. PMID:16609030 doi:10.1158/1078-0432.CCR-05-2235
  2. Bergman E, Forsell P, Persson EM, Knutson L, Dickinson P, Smith R, Swaisland H, Farmer MR, Cantarini MV, Lennernas H. Pharmacokinetics of gefitinib in humans: the influence of gastrointestinal factors. Int J Pharm. 2007 Aug 16;341(1-2):134-42. Epub 2007 Apr 6. PMID:17482782 doi:10.1016/j.ijpharm.2007.04.002
  3. D. Smith et al. Br J Clin Pharmacol. 2009 April; 67(4): 421–426.


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