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filingDate 2008-10-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 2011-01-06-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-2011500023-A
titleOfInvention Therapeutic siRNA molecules for reducing VEGFR1 expression in vitro and in vivo
abstract Improving the method for delivering RNAi-derived molecules in vivo is extremely important. It is also clear that delivering nucleic acid molecules that induce RNAi to the tissue as a target is crucial. It is also clear that the method of delivering nucleic acid molecules that induce RNAi selective for VEGF pathway genes is very beneficial for the treatment of NV disease. The compositions and methods of the present invention meet these needs. The present invention includes nucleic acid molecule compositions for use in modulating VEGF pathway gene expression and activity by RNA interference and reducing undesirable neovascularization, including tumor angiogenesis, and such nucleic acid molecules It relates to methods and compositions.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-2018225873-A1
priorityDate 2007-10-12-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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