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Thursday, July 19, 2007 2:32:10 PM
I’ve posted at length about the randomized head-to-head data showing Tyzeka superiority to Hepsera (#msg-21365649), which is the leading HBV drug in terms of sales.
The two-year resistance profile of Tyzeka in patients where the drug works is excellent—see #msg-14377860:
>>
“For telbivudine-treated patients who achieved PCR negativity at week 24, the per-protocol rates of resistance at two years were 4 percent in HBeAg-positive patients and 2 percent in HBeAg-negative patients. Per GLOBE study protocol, resistance was defined as HBV DNA return to >5 log, or to within 1 log of baseline.”
<<
The higher resistance figures in the references you cited are ITT figures, which are irrelevant for the reason mentioned in #msg-14403420: in patients where Tyzeka never works in the first place, it’s immaterial whether it induces strains that are resistant to Tyzeka because these patients will be switched to another therapy. There is no preclinical or clinical evidence I’m aware of that a short regimen of Tyzeka induces resistance to Baraclude or Hepsera.
Regarding HBV/HIV co-infected patients, this is a clear differentiating factor for Tyzeka because it has zero efficacy against HIV in animal models and thus it can’t cause premature resistance to HAART cocktails as Lamivudine, Baraclude, Hepsera, and Viread can. (The interferon drugs have this benefit too, but they are rarely used in HBV due to their poor therapeutic index.)
Lamivudine and Viread are approved drugs for HIV, Hepsera is a close chemical cousin of Viread, and Baraclude recently received a warning for its activity against HIV (#msg-17360663). With a modicum of marketing, Tyzeka should clearly become the HBV drug of choice in HBV/HIV co-infected patients.
All told, it’s clear that the AASLD guidelines you referenced either are obsolete (i.e. a googling error) or they should be obsolete. I will find out which.
“The efficient-market hypothesis may be
the foremost piece of B.S. ever promulgated
in any area of human knowledge!”
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