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


Journal

Antimicrobial agents and chemotherapy
ISSN: 1098-6596
Titre abrégé: Antimicrob Agents Chemother
Pays: United States
ID NLM: 0315061

Informations de publication

Date de publication:
04 2019
Historique:
received: 10 10 2018
accepted: 11 01 2019
pubmed: 13 2 2019
medline: 13 3 2020
entrez: 13 2 2019
Statut: epublish

Résumé

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 (

Identifiants

pubmed: 30745392
pii: AAC.02142-18
doi: 10.1128/AAC.02142-18
pmc: PMC6437487
pii:
doi:

Substances chimiques

Amides 0
Antiviral Agents 0
Benzofurans 0
Carbamates 0
Cyclopropanes 0
HIV Protease Inhibitors 0
Imidazoles 0
Intracellular Signaling Peptides and Proteins 0
NS3 protein, hepatitis C virus 0
NS4A cofactor peptide, Hepatitis C virus 0
Quinoxalines 0
Sulfonamides 0
Viral Nonstructural Proteins 0
Lopinavir 2494G1JF75
Atazanavir Sulfate 4MT4VIE29P
grazoprevir 4O2AB118LA
elbasvir 632L571YDK
NS-5 protein, hepatitis C virus EC 2.7.7.48
Ritonavir O3J8G9O825
Darunavir YO603Y8113

Types de publication

Clinical Trial, Phase I Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

Copyright © 2019 American Society for Microbiology.

Références

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Auteurs

Hwa-Ping Feng (HP)

Merck & Co., Inc., Kenilworth, New Jersey, USA hwa-ping.feng@merck.com.

Luzelena Caro (L)

Merck & Co., Inc., Kenilworth, New Jersey, USA.

Christine Fandozzi (C)

Merck & Co., Inc., Kenilworth, New Jersey, USA.

Xiaoyan Chu (X)

Merck & Co., Inc., Kenilworth, New Jersey, USA.

Zifang Guo (Z)

Merck & Co., Inc., Kenilworth, New Jersey, USA.

Jennifer Talaty (J)

Merck & Co., Inc., Kenilworth, New Jersey, USA.

Deborah Panebianco (D)

Merck & Co., Inc., Kenilworth, New Jersey, USA.

Katherine Dunnington (K)

Celerion, Inc., Lincoln, Nebraska, USA.

Lihong Du (L)

Merck & Co., Inc., Kenilworth, New Jersey, USA.

William D Hanley (WD)

Merck & Co., Inc., Kenilworth, New Jersey, USA.

Iain P Fraser (IP)

Merck & Co., Inc., Kenilworth, New Jersey, USA.

Anna Mitselos (A)

MSD Europe, Brussels, Belgium.

Jean-Francois Denef (JF)

MSD Europe, Brussels, Belgium.

Inge De Lepeleire (I)

MSD Europe, Brussels, Belgium.

Jan N de Hoon (JN)

Center for Clinical Pharmacology, University Hospitals Leuven, Leuven, Belgium.
Pharmaceutical and Pharmacological Sciences, KU Leuven, Leuven, Belgium.

Corinne Vandermeulen (C)

Pharmaceutical and Pharmacological Sciences, KU Leuven, Leuven, Belgium.

William L Marshall (WL)

Merck & Co., Inc., Kenilworth, New Jersey, USA.

Patricia Jumes (P)

Merck & Co., Inc., Kenilworth, New Jersey, USA.

Xiaobi Huang (X)

Merck & Co., Inc., Kenilworth, New Jersey, USA.

Monika Martinho (M)

Merck & Co., Inc., Kenilworth, New Jersey, USA.

Robert Valesky (R)

Merck & Co., Inc., Kenilworth, New Jersey, USA.

Joan R Butterton (JR)

Merck & Co., Inc., Kenilworth, New Jersey, USA.

Marian Iwamoto (M)

Merck & Co., Inc., Kenilworth, New Jersey, USA.

Wendy W Yeh (WW)

Merck & Co., Inc., Kenilworth, New Jersey, USA.

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Classifications MeSH