The FDA should eliminate the ambiguities in the current BCS biowaiver guidance and make public the drugs for which BCS biowaivers have been granted

Clin Pharmacol Ther. 2010 Sep;88(3):405-7. doi: 10.1038/clpt.2010.149. Epub 2010 Jul 28.

Abstract

Although US Food and Drug Administration (FDA)-approved Biopharmaceutics Classification System (BCS) class 1 drugs are designated as high-permeability drugs, in fact, the criterion utilized is high extent of absorption. This ambiguity should be eliminated, and the FDA criterion should explicitly be stated as > or =90% absorption based on absolute bioavailability or mass balance. Maintaining confidentiality regarding the drugs for which the FDA has approved BCS waivers of in vivo bioequivalence studies is not good public policy and should be reversed.

MeSH terms

  • Animals
  • Biological Availability
  • Biopharmaceutics / classification*
  • Drug Approval*
  • Humans
  • Intestinal Absorption
  • Permeability
  • Pharmaceutical Preparations / classification*
  • Pharmaceutical Preparations / metabolism
  • Solubility
  • Therapeutic Equivalency
  • United States
  • United States Food and Drug Administration

Substances

  • Pharmaceutical Preparations