Efficacy and Safety of Glecaprevir/Pibrentasvir in Chronic Hepatitis C Patients: Real-World Data

Introduction: Glecaprevir/pibrentasvir (G/P) is a pan-genotypic direct-acting antiviral therapy approved for use in adults with chronic hepatitis C virus (HCV) infection. This study aimed to assess the real-world efficacy and safety profile of G/P in individuals with chronic HCV. Materials and Meth...

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Bibliographic Details
Main Authors: Muhammet Rıdvan Tayşi, Yakup Gezer
Format: Article
Language:English
Published: Galenos Publishing House 2025-07-01
Series:Mediterranean Journal of Infection, Microbes and Antimicrobials
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Online Access:https://mjima.org/articles/efficacy-and-safety-of-glecaprevirpibrentasvir-in-chronic-hepatitis-c-patients-real-world-data/doi/mjima.galenos.2025.25430.12
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Summary:Introduction: Glecaprevir/pibrentasvir (G/P) is a pan-genotypic direct-acting antiviral therapy approved for use in adults with chronic hepatitis C virus (HCV) infection. This study aimed to assess the real-world efficacy and safety profile of G/P in individuals with chronic HCV. Materials and Methods: The analysis included patients over 18 years with detectable HCV-RNA who began G/P treatment for chronic HCV between January 1, 2021, and March 1, 2024. The primary outcome measure was sustained virologic response (SVR), defined as undetectable HCV-RNA 12 weeks after therapy completion. Safety and tolerability of the regimen were also evaluated. Results: G/P was administered to 191 patients, of whom 85.5% were male. Among them, 124 patients (64.9%) reported intravenous drug use. The most frequently identified genotype was GT 3 (57.1%). At 12 weeks post-treatment, 105 patients returned for follow-up, and all achieved SVR12. Adverse events occurred in 12 patients (6.3%). One patient discontinued treatment at week 4 due to pruritus and rash. Conclusion: G/P demonstrates high effectiveness, good tolerability, and a favorable safety profile as a pan-genotypic therapeutic option for chronic HCV infection.
ISSN:2147-673X