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Friday December 05 2008 | Biotechnology feed | All feeds
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In
the study, treatment with stabilized siRNA molecules (atuRNAi) through
clinically-relevant i .v . infusion
led to downregulation of a target which plays a significant role in regulating
glucose metabolism in vivo. Compared
to the control group, atuRNAi produced lower peak glucose levels with a return
to near normal levels after two hours. In
contrast, in animals treated with inactivated siRNA molecules, glucose levels
rose to very high levels and failed to revert to normal within two hours.
The
preclinical in vivo studies utilised a type II diabetes disease model in
which an insulin-independent signalling pathway was turned on.
Said Dr. Klaus Giese, “In this series of studies we have demonstrated
robust and very reproducible tissue
uptake and function of atugen’s proprietary siRNA therapeutic molecules. We
are now moving on to animal studies in various cancer models.” atugen’s
patent
application EP1389637 was published on atugen
AG,
(www.atugen.com) the Gene Silencing Company™,
is a biopharmaceutical company with core competence in functional gene
silencing. The company is based in GeneBloc®
and SignaLink™ are trademarks of atugen
AG.
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