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Author Notes:

Correspondence: Raymond F. Schinazi, Veterans Affairs Medical Center, Medical Research 151H, 1670 Clairmont Road, Decatur, GA 30033, USA; Email: rschina@emory.edu

Dr. Schinazi is a founder and a major shareholder of Pharmasset Inc., Idenix Pharmaceuticals Inc, and RFS Pharma LLC.


Research Funding:

This work was supported in part by NIH Grant 5R37-AI-041980, 4R37-AI-025899, R01-AI-076535, 5P30-AI- 50409 (CFAR), and by the Department of Veterans Affairs.


  • antiviral
  • drug
  • HCV
  • hepatitis C
  • inhibitors
  • therapy

HCV drug discovery aimed at viral eradication


Journal Title:

Journal of Viral Hepatitis


Volume 17, Number 2


, Pages 77-90

Type of Work:

Article | Post-print: After Peer Review


SUMMARY Hepatitis C virus (HCV) causes significant morbidity and mortality worldwide with nearly 3% of the world population infected by this virus. Fortunately, this virus does not establish latency, and hence it may be possible to eradicate it. HCV is strongly associated with liver cirrhosis and hepatocellular carcinoma and is currently treated with pegylated interferon-α (peg-IFN-α) and ribavirin. Unfortunately, these limited treatment options often produce significant side effects, and currently, complete eradication of virus with combined drug modalities has not yet been achieved for the majority of chronically HCV-infected individuals. Restricted treatment options, lack of a universal cure for HCV and the link between chronic infection, liver cirrhosis and hepatocellular carcinoma necessitate design of novel drugs and treatment options. Understanding the relationship between the immune response, viral clearance and inhibition of viral replication with pharmacology-based design can ultimately allow for complete eradication of HCV. This review focuses upon significant novel preclinical and clinical specifically targeted antiviral therapy (STAT-C) drugs under development, highlights their mechanism of action, and discusses their impact on systemic viral loads and permanent clearance of infection.

Copyright information:

© 2009 Blackwell Publishing Ltd

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