Pharmacokinetic and pharmacodynamic evaluation of raltegravir and experience from clinical trials in HIV-positive patients

Expert Opin Drug Metab Toxicol. 2015 Jul;11(7):1167-76. doi: 10.1517/17425255.2015.1056732.

Abstract

Introduction: Raltegravir was the first available integrase inhibitor for treating HIV-positive patients. This review aims to provide an overview of its role in the management of HIV-1 infection, highlighting its key pharmacokinetic and pharmacodynamic properties.

Areas covered: This review covers material searched and obtained through Medline and PubMed up to April 2015.

Expert opinion: Raltegravir for its tolerability, efficacy, few drug-to-drug interactions and for the amount of available data in difficult subgroups of patients is a key drug in the antiretroviral armamentarium. For its weak genetic barrier to resistance and erratic pharmacokinetic profile, it should be administered twice daily and with fully active companion antiretrovirals.

Keywords: drug-to-drug interactions; pharmacodynamic; pharmacokinetic; raltegravir; resistance.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Drug Interactions
  • Drug Resistance, Viral
  • HIV Infections / drug therapy*
  • HIV Integrase Inhibitors / pharmacokinetics
  • HIV Integrase Inhibitors / pharmacology
  • HIV Integrase Inhibitors / therapeutic use*
  • HIV-1 / drug effects
  • Humans
  • Raltegravir Potassium / pharmacokinetics
  • Raltegravir Potassium / pharmacology
  • Raltegravir Potassium / therapeutic use*

Substances

  • HIV Integrase Inhibitors
  • Raltegravir Potassium