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Friday, May 18, 2007 6:06:09 PM
I hadn't heard the news. Based on the statement below from a 10/06 review by Pawlotsky , I assumed entecavir was seeing some usage in lam-resistant patients :
http://clinicaloptions.com/Hepatitis/Treatment%20Updates/New%20Paradigm%20for%20HBV.aspx
Management of Resistance: Implications for Treatment Choice
Source: Focus on the Virus: A New Paradigm for the Management and Treatment of HBV
By: Jean-Michel Pawlotsky, MD, PhD
"One option for patients who develop resistance to lamivudine would be to switch to entecavir, which potently suppresses lamivudine-sensitive variants and also retains activity, albeit reduced, against lamivudine-resistant variants. However, given the risk of selecting additional “secondary” entecavir resistance mutations in lamivudine-resistant strains—which would lead to the loss of benefit from the switch—an alternative strategy is to continue lamivudine and add adefovir as a second drug or to switch to the combination of adefovir plus entecavir. If approved for the treatment of HBV, tenofovir will likely offer a good alternative to adefovir, since it exerts more potent antiviral activity than the 10 mg/day dose of adefovir."
To the extent that the battle is now between Hepsera and Tyzeka ( if it is , in fact ), I maintain that the victor is currently Hepsera based on scientific principles, until IDIX presents data to the contrary.
JMHO.
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