Hepatitis C virus drug resistance–associated substitutions: State of the art summary

Author:

Lontok Erik1,Harrington Patrick2,Howe Anita3,Kieffer Tara4,Lennerstrand Johan5,Lenz Oliver6,McPhee Fiona7,Mo Hongmei8,Parkin Neil9,Pilot‐Matias Tami10,Miller Veronica1

Affiliation:

1. Forum for Collaborative HIV Research, University of California at Berkeley,Washington,DC

2. Center for Drug Evaluation and Research, Office of Antimicrobial Products, Division of Antiviral Products, US Food and Drug Administration,Silver Spring,MD

3. Merck Research Laboratories,West Point,PA

4. Vertex Pharmaceuticals, Inc.,Boston,MA

5. Department of Medical Sciences,Uppsala University,Uppsala,Sweden

6. Janssen Infectious Diseases,Beerse,Belgium

7. Bristol‐Myers Squibb Research and Development,Wallingford,CT

8. Gilead Sciences, Inc.,Foster City,CA

9. Data First Consulting, Inc.,Belmont,CA

10. AbbVie, Inc.,Chicago,IL

Abstract

Hepatitis C virus (HCV) drug development has resulted in treatment regimens composed of interferon‐free, all‐oral combinations of direct‐acting antivirals. While the new regimens are potent and highly efficacious, the full clinical impact of HCV drug resistance, its implications for retreatment, and the potential role of baseline resistance testing remain critical research and clinical questions. In this report, we discuss the viral proteins targeted by HCV direct‐acting antivirals and summarize clinically relevant resistance data for compounds that have been approved or are currently in phase 3 clinical trials. Conclusion: This report provides a comprehensive, systematic review of all resistance information available from sponsors’ trials as a tool to inform the HCV drug development field. (Hepatology 2015;62:1623–1632)

Publisher

Ovid Technologies (Wolters Kluwer Health)

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