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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
Author(s) -
Hwa-ping Feng,
Luzelena Caro,
Christine Fandozzi,
Xiaoyan Chu,
Zifang Guo,
Jennifer Talaty,
Deborah Panebianco,
Katherine Dunnington,
Lihong Du,
William D. Hanley,
Iain P. Fraser,
Anna Mitselos,
JeanFrançois Denef,
Inge De Lepeleire,
Jan de Hoon,
Corinne Vandermeulen,
William L. Marshall,
Patricia Jumes,
Xiaobi Huang,
Monika Martinho,
Robert Valesky,
Joan R. Butterton,
Marian Iwamoto,
Wendy W. Yeh
Publication year - 2019
Publication title -
antimicrobial agents and chemotherapy
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.07
H-Index - 259
eISSN - 1070-6283
pISSN - 0066-4804
DOI - 10.1128/aac.02142-18
Subject(s) - ritonavir , darunavir , atazanavir , lopinavir , medicine , pharmacology , protease inhibitor (pharmacology) , virology , hepatitis c virus , pharmacokinetics , human immunodeficiency virus (hiv) , viral load , virus , antiretroviral therapy
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.

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