Nirmatrelvir and COVID-19: development, pharmacokinetics, clinical efficacy, resistance, relapse, and pharmacoeconomics

Int J Antimicrob Agents. 2023 Feb;61(2):106708. doi: 10.1016/j.ijantimicag.2022.106708. Epub 2023 Jan 2.

Abstract

Nirmatrelvir/ritonavir (N/R) is one of the most effective antiviral drugs against SARS-CoV-2. The preclinical development, pharmacodynamics and pharmacokinetics of N/R are reviewed herein. Randomized clinical trials have been conducted exclusively with pre-Omicron variants of concern, but in vitro studies show that efficacy against all Omicron sublineages is preserved, as confirmed by post-marketing observational studies. Nevertheless, investigations of large viral genome repositories have shown that mutation in the main protease causing resistance to N/R are increasingly frequent. In addition, virological and clinical rebounds after N/R discontinuation have been reported in immunocompetent patients. This finding is of concern when translated to immunocompromised patients, in whom N/R efficacy has not been formally investigated in clinical trials. Economical sustainability and perspectives for this therapeutic arena are discussed.

Keywords: Bexovid®; COVID-19; PF-00835231; PF-07321332; Paxlovid®; main protease; nirmatrelvir; protease inhibitors; ritonavir; small-chemical antivirals.

Publication types

  • Review

MeSH terms

  • Antiviral Agents / pharmacology
  • Antiviral Agents / therapeutic use
  • COVID-19 Drug Treatment
  • COVID-19*
  • Chronic Disease
  • Economics, Pharmaceutical
  • Humans
  • Recurrence
  • Ritonavir / therapeutic use
  • SARS-CoV-2
  • Treatment Outcome

Substances

  • Antiviral Agents
  • Ritonavir

Supplementary concepts

  • SARS-CoV-2 variants