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Who needs individual bioequivalence studies for narrow therapeutic index drugs? A case for warfarin

  • Avraham Yacobi
  • , Eric Masson
  • , Daniel Moros
  • , Derek Ganes
  • , Claude Lapointe
  • , Zohreh Abolfathi
  • , Marc LeBel
  • , Yechiel Golander
  • , Darlene Doepner
  • , Tamar Blumberg
  • , Yoram Cohen
  • , Barrie Levitt

Research output: Contribution to journalArticlepeer-review

23 Scopus citations

Abstract

Warfarin is, among drugs, considered to have a narrow therapeutic index for which individual bioequivalence has been suggested. To establish the propriety of 'switching, ' an individual bioequivalence study involving a replicate-design study and three 'switchings' in healthy subjects was undertaken using the U.S.-brand warfarin sodium tablet and a generic product. A randomized, single-center, open-label, single-dose, four-way crossover replicate bioequivalence study was performed in 24 healthy male volunteers in which each subject received the same 5 mg warfarin test and reference tablets twice on different occasions under fasting conditions. Concentrations of warfarin in plasma were measured by a validated specific HPLC method. The individual pharmacokinetic parameters obtained with test and reference products were compared using pooled data and Liu's method. Bioequivalence was shown with both average and individual bioequivalence methods. The individual bioequivalence assessment did not show a subject-by-formulation interaction, nor did it add value to the bioequivalence assessment of warfarin. (C) 2000 the American College of Clinical Pharmacology.

Original languageEnglish
Pages (from-to)826-835
Number of pages10
JournalJournal of Clinical Pharmacology
Volume40
Issue number8
DOIs
StatePublished - 2000

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