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Gilead announces 144-week data of Hepsera in patients co-infected with HIV and lamivudine-resistant HBV.

Asia Africa Intelligence Wire

| October 28, 2003 | COPYRIGHT 2003 Financial Times Ltd. (Hide copyright information)Copyright

(From Chemical Business NewsBase - Press Release)

Gilead Sciences announced that treatment with its once-daily, oral antiviral agent Hepsera (adefovir dipivoxil 10 mg) was associated with sustained reductions in levels of hepatitis B virus (HBV) DNA through 144 weeks among patients chronically infected with lamivudine-resistant HBV and co-infected with HIV. Data from the single-centre, open-label clinical trial (Study 460i) were presented at the 54th Annual Meeting of the American Association for the Study of Liver Diseases (AASLD) in Boston, MA. Study 460i is a single-centre, open-label study of Hepsera in chronic hepatitis B patients with lamivudine-resistant HBV and …

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