Pharmacokinetic Interactions between the Hepatitis C Virus Inhibitors Elbasvir and Grazoprevir and HIV Protease Inhibitors Ritonavir, Atazanavir, Lopinavir, and Darunavir in Healthy Volunteers

Antimicrob Agents Chemother. 2019 Mar 27;63(4):e02142-18. doi: 10.1128/AAC.02142-18. Print 2019 Apr.

Abstract

The combination of the hepatitis C virus (HCV) nonstructural protein 5A (NS5A) inhibitor elbasvir and the NS3/4A protease inhibitor grazoprevir is a potent, once-daily therapy indicated for the treatment of chronic HCV infection in individuals coinfected with human immunodeficiency virus (HIV). We explored the pharmacokinetic interactions of elbasvir and grazoprevir with ritonavir and ritonavir-boosted HIV protease inhibitors in three phase 1 trials. Drug-drug interaction trials with healthy participants were conducted to evaluate the effect of ritonavir on the pharmacokinetics of grazoprevir (n = 10) and the potential two-way pharmacokinetic interactions of elbasvir (n = 30) or grazoprevir (n = 39) when coadministered with ritonavir-boosted atazanavir, lopinavir, or darunavir. Coadministration of ritonavir with grazoprevir increased grazoprevir exposure; the geometric mean ratio (GMR) for grazoprevir plus ritonavir versus grazoprevir alone area under the concentration-time curve from 0 to 24 h (AUC0-24) was 1.91 (90% confidence interval [CI]; 1.31 to 2.79). Grazoprevir exposure was markedly increased with coadministration of atazanavir-ritonavir, lopinavir-ritonavir, and darunavir-ritonavir, with GMRs for grazoprevir AUC0-24 of 10.58 (90% CI, 7.78 to 14.39), 12.86 (90% CI, 10.25 to 16.13), and 7.50 (90% CI, 5.92 to 9.51), respectively. Elbasvir exposure was increased with coadministration of atazanavir-ritonavir, lopinavir-ritonavir, and darunavir-ritonavir, with GMRs for elbasvir AUC0-24 of 4.76 (90% CI, 4.07 to 5.56), 3.71 (90% CI, 3.05 to 4.53), and 1.66 (90% CI, 1.35 to 2.05), respectively. Grazoprevir and elbasvir had little effect on atazanavir, lopinavir, and darunavir pharmacokinetics. Coadministration of elbasvir-grazoprevir with atazanavir-ritonavir, lopinavir-ritonavir, or darunavir-ritonavir is contraindicated, owing to an increase in grazoprevir exposure. Therefore, HIV treatment regimens without HIV protease inhibitors should be considered for HCV/HIV-coinfected individuals who are being treated with elbasvir-grazoprevir.

Keywords: atazanavir; darunavir; elbasvir; grazoprevir; lopinavir; ritonavir; virology.

Publication types

  • Clinical Trial, Phase I

MeSH terms

  • Adult
  • Amides
  • Antiviral Agents / pharmacokinetics*
  • Antiviral Agents / pharmacology
  • Atazanavir Sulfate / pharmacokinetics
  • Atazanavir Sulfate / pharmacology
  • Benzofurans / pharmacokinetics
  • Benzofurans / pharmacology
  • Carbamates
  • Cyclopropanes
  • Darunavir / pharmacokinetics
  • Darunavir / pharmacology
  • Drug Interactions
  • Female
  • HIV Infections / drug therapy*
  • HIV Protease Inhibitors / pharmacokinetics*
  • HIV Protease Inhibitors / pharmacology
  • HIV-1 / drug effects
  • Healthy Volunteers
  • Hepacivirus / drug effects
  • Hepatitis C / drug therapy*
  • Humans
  • Imidazoles / pharmacokinetics
  • Imidazoles / pharmacology
  • Intracellular Signaling Peptides and Proteins / antagonists & inhibitors
  • Lopinavir / pharmacokinetics
  • Lopinavir / pharmacology
  • Male
  • Middle Aged
  • Quinoxalines / pharmacokinetics
  • Quinoxalines / pharmacology
  • Ritonavir / pharmacokinetics
  • Ritonavir / pharmacology
  • Sulfonamides
  • Viral Nonstructural Proteins / antagonists & inhibitors
  • Young Adult

Substances

  • Amides
  • Antiviral Agents
  • Benzofurans
  • Carbamates
  • Cyclopropanes
  • HIV Protease Inhibitors
  • Imidazoles
  • Intracellular Signaling Peptides and Proteins
  • NS3 protein, hepatitis C virus
  • NS4A cofactor peptide, Hepatitis C virus
  • Quinoxalines
  • Sulfonamides
  • Viral Nonstructural Proteins
  • Lopinavir
  • Atazanavir Sulfate
  • grazoprevir
  • elbasvir
  • NS-5 protein, hepatitis C virus
  • Ritonavir
  • Darunavir