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the enhancement of the apoptotic effect when added to either
vincristine or fludarabine. The other poster reported that in vivo
immunostimulatory responses to ANA773 can be effectively modified by
varying the schedule of dose administration, including every other day
dosing (QOD), and three consecutive days of dosing within each seven
day cycle (3-on, 4-off).
Program Updates and Revised Cash Outlook for 2008
-- ANA598 Development Activities. Based on promising results from the
preclinical evaluation of ANA598, Anadys has made the strategic
decision to accelerate certain non-clinical activities for this
program, including further manufacturing of drug substance and
conducting additional toxicology studies. These studies include a
combination toxicology study with ribavirin that will support the
clinical investigation of ANA598 in combination with interferon and
ribavirin, as well as studies extending the duration of dosing beyond
the recently completed 28 day toxicology study. If ANA598 is
successful in early stage clinical trials, it is anticipated that the
acceleration of these non-clinical activities into 2008 will enable a
more rapid and continuous development path into mid-stage clinical
trials during 2009.
-- ANA773 Development Activities. Anadys continues to explore the safety
and tolerability profile of ANA773 in the ongoing Phase I trial and
expects to identify pharmacologically active doses and establish the
profile of immune stimulation this year, which information will support
the future design of clinical trials of ANA773 (alone or in
combinations) in specific tumor types. While Anadys expects the rate
of enrollment in the ANA773 oncology trial to increase in the coming
quarters, the Company now expects the pac
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| SOURCE Anadys Pharmaceuticals, Inc. Copyright©2008 PR Newswire. All rights reserved |