Chen‐Hua LiuYu‐Lueng ShihSheng‐Shun YangChih‐Lin LinYu‐Jen FangPin‐Nan ChengChi‐Yi ChenCheng‐Yuan PengTsai‐Yuan HsiehYen‐Cheng ChiuTung‐Hung SuChun‐Jen LiuHung‐Chih YangPei‐Jer ChenDing‐Shinn ChenJia‐Horng Kao2026-01-302026-01-302019-05-2710.1111/jgh.14672https://scholars.csmu.edu.tw/handle/123456789/3909<jats:title>Abstract</jats:title><jats:sec><jats:title>Background and Aim</jats:title><jats:p>Data regarding the efficacy and safety of paritaprevir/ritonavir, ombitasvir plus dasabuvir (PrOD) for East Asian non‐cirrhotic hepatitis C virus genotype 1b (HCV GT1b) patients receiving hemodialysis were limited.</jats:p></jats:sec><jats:sec><jats:title>Methods</jats:title><jats:p>Forty‐six HCV GT1b non‐cirrhotic patients receiving hemodialysis who received PrOD for 12 weeks were prospectively enrolled in seven academic centers in Taiwan. The primary efficacy endpoint was sustained virologic response 12 weeks off‐therapy (SVR<jats:sub>12</jats:sub>). Patients' baseline characteristics, early virokinetics, and HCV resistance‐associated substitutions (RASs) potentially related to SVR<jats:sub>12</jats:sub> were analyzed. The safety profiles were also assessed.</jats:p></jats:sec><jats:sec><jats:title>Results</jats:title><jats:p>The SVR<jats:sub>12</jats:sub> rate was 100% (46 of 46 patients). Patients' baseline characteristics, on‐treatment viral decline, and baseline HCV resistance‐associated substitutions did not affect SVR<jats:sub>12</jats:sub>. All patients tolerated treatment well. One patient with folliculitis temporarily discontinued treatment, and another two patients had serious adverse events (SAEs), which were considered not related to PrOD treatment. The common adverse events were pruritus (19.6%), fatigue (15.2%), and upper respiratory tract infection (6.5%). Twelve (19.6%) and one (2.2%) patients had hemoglobin levels &lt; 10 and 8.5 g/dL, respectively, which were related to renal impairment. Five (10.9%) patients had on‐treatment total bilirubin level of 1.5–3.0 mg/dL, but none developed hepatic decompensation. The bilirubin levels peaked at week 1 of treatment and then declined with continuous treatment.</jats:p></jats:sec><jats:sec><jats:title>Conclusion</jats:title><jats:p>Treatment with PrOD for 12 weeks is efficacious and well‐tolerated for East Asian non‐cirrhotic HCV GT1b patients receiving hemodialysis.</jats:p></jats:sec>[SDGs]SDG3journal-article