Efficacy and Safety of Glecaprevir/Pibrentasvir in Patients with Chronic HCV Infection.
Xiaoqing LiuPeng HuPublished in: Journal of clinical and translational hepatology (2021)
Hepatitis C virus (HCV) infection is a major cause of end-stage liver disease, including decompensated cirrhosis and hepatocellular carcinoma. Over 95% of patients with HCV infection have achieved sustained virologic response at 12 weeks under the treatment of several pan-genotypic regimens approved for patients with HCV infection. The glecaprevir/pibrentasvir (G/P) regimen has some features that distinguish it from others and is the only 8-week regimen approved for treatment-naive patients and patients experienced in regimens containing (peg)interferon, ribavirin, and/or sofosbuvir, without an HCV NS3/4A protease inhibitor or NS5A inhibitor (except those with genotype 3). This review aims to summarize the efficacy and safety of G/P in HCV-infected patients from clinic trials and real-world studies, including those who have historically been considered difficult to cure.
Keyphrases
- hepatitis c virus
- human immunodeficiency virus
- end stage renal disease
- ejection fraction
- newly diagnosed
- chronic kidney disease
- heart failure
- peritoneal dialysis
- prognostic factors
- hiv infected
- patient reported outcomes
- clinical trial
- hepatitis b virus
- drug administration
- immune response
- smoking cessation
- combination therapy
- atrial fibrillation
- gestational age
- double blind
- preterm birth