Switch from enfuvirtide to raltegravir lowers plasma concentrations of darunavir and tipranavir: a pharmacokinetic substudy of the EASIER-ANRS 138 trial

Antimicrob Agents Chemother. 2011 Jul;55(7):3613-5. doi: 10.1128/AAC.01827-10. Epub 2011 May 16.

Abstract

We compared tipranavir and darunavir concentrations measured at steady state in 20 human immunodeficiency virus (HIV)-infected patients enrolled in the EASIER-ANRS 138 clinical trial who switched from enfuvirtide to raltegravir while maintaining the same background regimen. The geometric mean ratios of the observed predose concentration (C(trough)), maximum concentration of drug observed in plasma (C(max)), and area under the plasma concentration-time curve (AUC) before (day 0) and after (week 24) the switch were 0.49, 0.76, and 0.67 and 0.82, 0.68, and 0.64 for tipranavir and darunavir, respectively. The virologic consequences of these drug interactions have yet to be determined.

MeSH terms

  • Anti-HIV Agents / blood
  • Anti-HIV Agents / pharmacokinetics*
  • Anti-HIV Agents / therapeutic use
  • Darunavir
  • Enfuvirtide
  • Female
  • HIV Envelope Protein gp41 / blood
  • HIV Envelope Protein gp41 / pharmacokinetics*
  • HIV Envelope Protein gp41 / therapeutic use
  • HIV Infections / blood
  • HIV Infections / drug therapy*
  • Humans
  • Male
  • Middle Aged
  • Peptide Fragments / blood
  • Peptide Fragments / pharmacokinetics*
  • Peptide Fragments / therapeutic use
  • Pyridines / blood
  • Pyridines / pharmacokinetics*
  • Pyridines / therapeutic use
  • Pyrones / blood
  • Pyrones / pharmacokinetics*
  • Pyrones / therapeutic use
  • Ritonavir / blood
  • Ritonavir / pharmacokinetics*
  • Ritonavir / therapeutic use
  • Sulfonamides / blood
  • Sulfonamides / pharmacokinetics*
  • Sulfonamides / therapeutic use

Substances

  • Anti-HIV Agents
  • HIV Envelope Protein gp41
  • Peptide Fragments
  • Pyridines
  • Pyrones
  • Sulfonamides
  • Enfuvirtide
  • Ritonavir
  • Darunavir
  • tipranavir