Abstract
No new therapy has been approved for the treatment of chronic hepatitis C in the last 5 years in the USA since the approval of pegylated interferon (IFN)-α2a and ribavirin. Multiple new drugs are currently in development and are expected to be approved for use in the USA and/or the EU by 2011–2013. Although the mechanism of action of pegylated IFN and ribavirin are not completely known, it is likely that they will continue to be used in combination regimens for a number of years. Direct antivirals are likely to be the first new drugs to be used in combination with pegylated IFN and ribavirin. Viral resistance will prove to be a significant barrier and require that consolidation therapy with at least 24 weeks of pegylated IFN and ribavirin be used to successfully prevent the selection or emergence of resistant variants. Numerous other compounds, such as ribavirin analogs, long-acting IFNs, hepatoprotectants and immunomodulators, are in development and may replace the drugs that are used currently. The combination of direct antivirals, such as protease and polymerase inhibitors, may rapidly follow in development, as has occurred in HIV drug therapy.
Financial & competing interests disclosure
The author has received research grants from Human Genome Sciences, Novartis, Valeant, Intermune, Sciclone, Vernalis, Schering–Plough, Roche, Idenix, Wyeth, Debio, Idun, Migenix, Glaxo Smith Kline, Isis and Ribozyme. He has also acted as a consultant for Novartis, Valeant, Intermune, Sciclone, Vernalis, Schering–Plough, Roche, Idenix, Wyeth, Idun, Migenix and Tacere. The author is a speaker for Novartis, Valeant, Schering-Plough, Roche and Idenix. CME grants have been received from Human Genome Sciences, Novartis, Valeant, Schering–Plough, Roche and Idenix. The authors have no other relevant affiliations or financial involvement with any organization or entity with a financial interest in or financial conflict with the subject matter or materials discussed in the manuscript apart from those disclosed.
No writing assistance was utilized in the production of this manuscript.