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Effectiveness and safety of 8-week glecaprevir/pibrentasvir in HCV treatment-naïve patients with compensated cirrhosis: real-world experience from Taiwan nationwide HCV registry.

Te-Sheng ChangChung-Feng HuangHsing-Tao KuoChing-Chu LoChien-Wei HuangLee-Won ChongPin-Nan ChengMing-Lun YehCheng-Yuan PengChien-Yu ChengJee-Fu HuangMing-Jong BairChih-Lang LinChi-Chieh YangSzu-Jen WangTsai-Yuan HsiehTzong-Hsi LeePei-Lun LeeWen-Chih WuChih-Lin LinWei-Wen SuSheng-Shun YangChia-Chi WangJui-Ting HuLein-Ray MoChun-Ting ChenYi-Hsiang HuangChun-Chao ChangChia-Sheng HuangGuei-Ying ChenChien-Neng KaoChi-Ming TaiChun-Jen LiuMei-Hsuan LeePei-Chien TsaiChia-Yen DaiJia-Horng KaoHan-Chieh LinWang-Long ChuangChi-Yi ChenKuo-Chih TsengChao-Hung HungMing-Lung Yu
Published in: Hepatology international (2023)
In this large-scale real-world Taiwanese cohort, 8-week GLE/PIB therapy was efficacious and well tolerated for treatment-naïve compensated cirrhosis patients. SVR12 rates were similarly high as in the clinical trials, including those with characteristics of advanced liver disease.
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