{"title":"Telaprevir: new specific protease inhibitor for chronic hepatitis C","authors":"Geoffrey Dusheiko MB BCh FCP(SA) FRCP FRCP (edin)","doi":"10.1002/fps.83","DOIUrl":null,"url":null,"abstract":"<p><b>Current treatment for hepatitis C virus (HCV) genotype 1 infection with pegylated interferon (PEG-IFN) and ribavirin (RBV) is effective in less than 50% of patients. Retreatment with the same regimen is poorly effective. The advent of direct-acting antiviral agents that target replication of HCV promises to improve therapy for the disease. Telaprevir is a new protease inhibitor that specifically targets the NS3/4A serine protease, rapidly reducing HCV ribonucleic acid (RNA) levels. Several phase 2 and phase 3 studies have assessed the efficacy and safety of telaprevir. The author discusses the results of these studies, which suggest that the addition of this specific protease inhibitor to PEG-IFN-alpha2 and RBV can signifi cantly improve the results of treatment in patients affected with chronic HCV infection with genotype 1, compared with the standard treatment.</b> Copyright © 2011 John Wiley & Sons, Ltd.</p>","PeriodicalId":100566,"journal":{"name":"Future Prescriber","volume":"12 3","pages":"19-23"},"PeriodicalIF":0.0000,"publicationDate":"2011-10-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1002/fps.83","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Future Prescriber","FirstCategoryId":"1085","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/fps.83","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Current treatment for hepatitis C virus (HCV) genotype 1 infection with pegylated interferon (PEG-IFN) and ribavirin (RBV) is effective in less than 50% of patients. Retreatment with the same regimen is poorly effective. The advent of direct-acting antiviral agents that target replication of HCV promises to improve therapy for the disease. Telaprevir is a new protease inhibitor that specifically targets the NS3/4A serine protease, rapidly reducing HCV ribonucleic acid (RNA) levels. Several phase 2 and phase 3 studies have assessed the efficacy and safety of telaprevir. The author discusses the results of these studies, which suggest that the addition of this specific protease inhibitor to PEG-IFN-alpha2 and RBV can signifi cantly improve the results of treatment in patients affected with chronic HCV infection with genotype 1, compared with the standard treatment. Copyright © 2011 John Wiley & Sons, Ltd.
特拉匹韦:治疗慢性丙型肝炎的新型特异性蛋白酶抑制剂
目前,聚乙二醇化干扰素(PEG-IFN)和利巴韦林(RBV)治疗丙型肝炎病毒(HCV)基因1型感染的有效性不足50%。用同样的治疗方案再治疗效果很差。针对丙型肝炎病毒复制的直接抗病毒药物的出现有望改善该疾病的治疗。Telaprevir是一种新的蛋白酶抑制剂,专门针对NS3/4A丝氨酸蛋白酶,快速降低HCV核糖核酸(RNA)水平。几项2期和3期研究已经评估了telaprevir的有效性和安全性。作者对这些研究结果进行了讨论,结果表明,与标准治疗相比,在PEG-IFN-alpha2和RBV中加入这种特异性蛋白酶抑制剂可显著改善基因1型慢性HCV感染患者的治疗效果。版权所有©2011 John Wiley &儿子,有限公司
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