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US Patent 10167471 Inhibition of PCSK9 through RNAI

Patent 10167471 was granted and assigned to Rxi Pharmaceuticals Corporation on January, 2019 by the United States Patent and Trademark Office.

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Is a
Patent
Patent
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Patent attributes

Patent Applicant
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Rxi Pharmaceuticals Corporation
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Current Assignee
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Rxi Pharmaceuticals Corporation
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Patent Jurisdiction
United States Patent and Trademark Office
United States Patent and Trademark Office
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Patent Number
101674710
Patent Inventor Names
Anastasia Khvorova0
Joanne Kamens0
Date of Patent
January 1, 2019
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Patent Application Number
152869480
Date Filed
October 6, 2016
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Patent Citations Received
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US Patent 11926828 Methods for treating aging and skin disorders using nucleic acids targeting TYR or MMP1
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US Patent 11021707 Reduced size self-delivering nucleic acid compounds targeting long non-coding RNA
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US Patent 11254940 Inhibition of MAP4K4 through RNAi
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US Patent 11279934 Methods for treating cancer using nucleic acids targeting MDM2 or MYCN
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US Patent 11667915 RNA duplexes with single stranded phosphorothioate nucleotide regions for additional functionality
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US Patent 11396654 Neutral nanotransporters
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US Patent 10479992 RNA duplexes with single stranded phosphorothioate nucleotide regions for additional functionality
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US Patent 10633654 Modified RNAi polynucleotides and uses thereof
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Patent Primary Examiner
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Amy H Bowman
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Patent abstract

The invention relates to various PCSK9 RNAi constructs with gene silencing activities, and uses thereof. The construct has a double-stranded region of 19-49 nucleotides, preferably 25, 26, or 27 nucleotides, and preferably blunt-ended. The construct has selective minimal modifications to confer an optimal balance of biological activity, toxicity, stability, and target gene specificity. The sense strand may be modified such that the construct is not cleaved by Dicer or other RNAse III, and the entire length of the antisense strand is loaded into RISC In addition, the antisense strand may also be modified by 2′-O-methyl groups at the 2nd 5′-end nucleotide to greatly reduce off-target silencing. The constructs of the invention largely avoid the interferon response and sequence-independent apoptosis in mammalian cells, exhibits better serum stability, and enhanced target specificity.

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