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- W2014202267 endingPage "598" @default.
- W2014202267 startingPage "588" @default.
- W2014202267 abstract "The inclusion of NS3 protease inhibitors to the interferon-containing standard of care improved sustained viral response rates in hepatitis C virus (HCV) infected patients. However, there is still an unmet medical need as this drug regimen is poorly tolerated and lacks efficacy, especially in difficult-to-treat patients. Intense drug discovery and development efforts have focused on direct-acting antivirals (DAA) that target NS3 protease, NS5B polymerase and the NS5A protein. DAA combinations are currently assessed in clinical trials. Alternative antivirals have emerged that target host machineries co-opted by HCV. Finally, continuous and better understanding of HCV biology allows speculating on the value of novel classes of DAA required in future personalized all-oral interferon-free combination therapy and for supporting global disease eradication." @default.
- W2014202267 created "2016-06-24" @default.
- W2014202267 creator A5003624511 @default.
- W2014202267 creator A5046764938 @default.
- W2014202267 creator A5049894159 @default.
- W2014202267 creator A5073065189 @default.
- W2014202267 date "2012-10-01" @default.
- W2014202267 modified "2023-10-13" @default.
- W2014202267 title "Direct-acting and host-targeting HCV inhibitors: current and future directions" @default.
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