Tecarfarin, a novel vitamin K reductase antagonist, is not affected by CYP2C9 and CYP3A4 inhibition following concomitant administration of fluconazole in healthy participants

J Clin Pharmacol. 2011 Apr;51(4):561-74. doi: 10.1177/0091270010370588. Epub 2010 Jul 9.

Abstract

Comparative pharmacokinetics of vitamin K epoxide reductase antagonists tecarfarin and warfarin were assessed before and after coadministration for 21 days of the CYP450 inhibitor fluconazole in a randomized, open-label, single-center drug interaction study. Twenty healthy adult participants were randomized 1:1 to receive approximately equipotent single oral doses of tecarfarin (50 mg) or warfarin (17.5 mg). Following 7 days of baseline serial blood level collections, each participant received oral fluconazole 400 mg daily for 21 days. A second identical single oral dose of tecarfarin or warfarin was given 14 days after starting fluconazole with serial pharmacokinetic sampling. Key pharmacokinetic parameters C(max), t(max), AUC(0-168), apparent clearance, and t(1/2) demonstrated no tecarfarin-fluconazole interaction but a strong warfarin-fluconazole interaction. The ratio of log-transformed mean AUC(0-168) with versus without fluconazole for tecarfarin was 91.2% (90% confidence interval [CI]: 83.3-99.8) and for racemic warfarin was 213% (90% CI: 202-226). The 90% CI was entirely within the standard 80% to 125% bioequivalence interval for tecarfarin but well outside the bioequivalence interval for warfarin, confirming a clinically significant pharmacokinetic interaction between warfarin and fluconazole. In contrast, tecarfarin pharmacokinetics were apparently unchanged by fluconazole.

Publication types

  • Randomized Controlled Trial
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Administration, Oral
  • Adult
  • Aryl Hydrocarbon Hydroxylases / antagonists & inhibitors*
  • Benzoates / administration & dosage
  • Benzoates / pharmacokinetics*
  • Coumarins / administration & dosage
  • Coumarins / pharmacokinetics*
  • Cytochrome P-450 CYP2C9
  • Cytochrome P-450 CYP3A
  • Cytochrome P-450 CYP3A Inhibitors*
  • Drug Interactions
  • Enzyme Inhibitors / pharmacology
  • Female
  • Fluconazole / pharmacology*
  • Humans
  • Male
  • NAD(P)H Dehydrogenase (Quinone) / antagonists & inhibitors
  • Warfarin / administration & dosage
  • Warfarin / pharmacokinetics

Substances

  • Benzoates
  • Coumarins
  • Cytochrome P-450 CYP3A Inhibitors
  • Enzyme Inhibitors
  • Warfarin
  • Fluconazole
  • CYP2C9 protein, human
  • Cytochrome P-450 CYP2C9
  • Aryl Hydrocarbon Hydroxylases
  • Cytochrome P-450 CYP3A
  • CYP3A4 protein, human
  • NAD(P)H Dehydrogenase (Quinone)
  • tecarfarin