Published in:
Open Access
01-12-2010 | Oral presentation
0311. Hepatitis C new drugs
Author:
H Wedemeyer
Published in:
Journal of the International AIDS Society
|
Special Issue 4/2010
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Excerpt
Hepatitis C virus infection remains a significant global health problem with more than 130 Million individuals being chronically infected world-wide. Since 2001, the standard therapy of chronic hepatitis has been PEG-IFNa + ribavirin. A large number of new direct acting antiviral agents is currently explored in clinical trials. Different viral proteins are targeted by these novel agents. The first HCV protease inhibitors telaprevir and boceprevir are expected to be approved in 2011 as phase III trials have been completed in summer 2010. At this stage, Direct Acting Anti-Viral agents will only be used in combination with PEG-IFNa and ribavirin. Triple therapy will increase sustained virological response rates by 25-30% for treatment naïve patients infected with HCV genotype 1 to 70-80% and previous nonresponder patients may now have chance of 30-50% to cure the infection. Moreover, treatment will be “response guided” meaning that patients who are already HCV RNA negative by week 4 can be treated shorter for only 24-28 weeks while slow responder still have to treated for 48 weeks. Resistance will be a problem for first generation HCV protease inhibitors, in particular if only suboptimal doses of PEG-IFNa and ribavirin can be administered. Finally, the new drugs will add additional side effects as telaprevir may cause rashes in 5-10% of patients and boceprevir can induce nausea. Both drugs can induce anaemia which may be more pronounced for boceprevir. …