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Pharmacokinetic Interactions between the Hepatitis C Virus Inhibitors Elbasvir and Grazoprevir and HIV Protease Inhibitors Ritonavir, Atazanavir, Lopinavir, and Darunavir in Healthy Volunteers.
Feng, Hwa-Ping; Caro, Luzelena; Fandozzi, Christine; Chu, Xiaoyan; Guo, Zifang; Talaty, Jennifer; Panebianco, Deborah; Dunnington, Katherine; Du, Lihong; Hanley, William D; Fraser, Iain P; Mitselos, Anna; Denef, Jean-Francois; De Lepeleire, Inge; de Hoon, Jan N; Vandermeulen, Corinne; Marshall, William L; Jumes, Patricia; Huang, Xiaobi; Martinho, Monika; Valesky, Robert; Butterton, Joan R; Iwamoto, Marian; Yeh, Wendy W.
Afiliación
  • Feng HP; Merck & Co., Inc., Kenilworth, New Jersey, USA hwa-ping.feng@merck.com.
  • Caro L; Merck & Co., Inc., Kenilworth, New Jersey, USA.
  • Fandozzi C; Merck & Co., Inc., Kenilworth, New Jersey, USA.
  • Chu X; Merck & Co., Inc., Kenilworth, New Jersey, USA.
  • Guo Z; Merck & Co., Inc., Kenilworth, New Jersey, USA.
  • Talaty J; Merck & Co., Inc., Kenilworth, New Jersey, USA.
  • Panebianco D; Merck & Co., Inc., Kenilworth, New Jersey, USA.
  • Dunnington K; Celerion, Inc., Lincoln, Nebraska, USA.
  • Du L; Merck & Co., Inc., Kenilworth, New Jersey, USA.
  • Hanley WD; Merck & Co., Inc., Kenilworth, New Jersey, USA.
  • Fraser IP; Merck & Co., Inc., Kenilworth, New Jersey, USA.
  • Mitselos A; MSD Europe, Brussels, Belgium.
  • Denef JF; MSD Europe, Brussels, Belgium.
  • De Lepeleire I; MSD Europe, Brussels, Belgium.
  • de Hoon JN; Center for Clinical Pharmacology, University Hospitals Leuven, Leuven, Belgium.
  • Vandermeulen C; Pharmaceutical and Pharmacological Sciences, KU Leuven, Leuven, Belgium.
  • Marshall WL; Pharmaceutical and Pharmacological Sciences, KU Leuven, Leuven, Belgium.
  • Jumes P; Merck & Co., Inc., Kenilworth, New Jersey, USA.
  • Huang X; Merck & Co., Inc., Kenilworth, New Jersey, USA.
  • Martinho M; Merck & Co., Inc., Kenilworth, New Jersey, USA.
  • Valesky R; Merck & Co., Inc., Kenilworth, New Jersey, USA.
  • Butterton JR; Merck & Co., Inc., Kenilworth, New Jersey, USA.
  • Iwamoto M; Merck & Co., Inc., Kenilworth, New Jersey, USA.
  • Yeh WW; Merck & Co., Inc., Kenilworth, New Jersey, USA.
Article en En | MEDLINE | ID: mdl-30745392
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.
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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Antivirales / Infecciones por VIH / Hepatitis C / Inhibidores de la Proteasa del VIH Idioma: En Revista: Antimicrob Agents Chemother Año: 2019 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Antivirales / Infecciones por VIH / Hepatitis C / Inhibidores de la Proteasa del VIH Idioma: En Revista: Antimicrob Agents Chemother Año: 2019 Tipo del documento: Article País de afiliación: Estados Unidos