US2013177631A1PendingUtilityA1

Method and medicament for inhibiting the expression of a given gene

Assignee: ALNYLAM PHARMACEUTICALS INCPriority: Jan 30, 1999Filed: Jan 29, 2013Published: Jul 11, 2013
Est. expiryJan 30, 2019(expired)· nominal 20-yr term from priority
A61P 43/00C12N 2310/53C12N 15/113C12N 2310/111A61P 31/04A61P 31/10A61P 31/20A61P 31/00C12N 2310/14A61K 38/00A61P 35/00A61P 31/12C12N 2330/30C12N 15/111A61P 25/28A61K 31/713Y02A50/30
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Claims

Abstract

The invention relates to an oligoribonucleotide of double-stranded structure (dsRNA) for inhibiting the expression of a given target gene in mammalian cells and a method of mediating RNA interference of an mRNA of a gene in mammalian cells using the dsRNA.

Claims

exact text as granted — not AI-modified
1 . An oligoribonucleotide of double-stranded structure (dsRNA) for inhibiting the expression of a given target gene in mammalian cells, wherein the dsRNA has 15 to 49 base pairs and has a complementary region I that is incorporated in the dsRNA, and wherein the complementary region I has not more than 49 nucleotide pairs. 
     
     
         2 . The dsRNA of  claim 1 , wherein at least one of said strands comprises at least one chemically modified nucleotide. 
     
     
         3 . The dsRNA of  claim 2 , wherein said chemically modified nucleotide is a 2′-modified nucleotide. 
     
     
         4 . The dsRNA of  claim 3 , wherein said 2′-modified nucleotide is a 2′-methyl substituted nucleotide. 
     
     
         5 . The dsRNA of  claim 3 , wherein said 2′-modified nucleotide is a 2′-amino substituted nucleotide. 
     
     
         6 . The dsRNA of  claim 3 , wherein said chemically modified nucleotide is a locked nucleotide. 
     
     
         7 . The dsRNA of  claim 1 , wherein the target gene is a mammalian gene or a viral gene. 
     
     
         8 . The dsRNA of  claim 1 , wherein the target gene is selected from the group consisting of an oncogene, a cytokine gene, an Id protein gene, a developmental gene, a PKR gene and a prion gene. 
     
     
         9 . The dsRNA of  claim 1 , wherein inhibiting the expression of said target gene further comprises inhibiting expression at a concentration of the dsRNA that is lower by one order of magnitude than a concentration required for a corresponding single-stranded oligoribonucleotide to inhibit expression. 
     
     
         10 . The dsRNA of  claim 1 , wherein the dsRNA is enclosed by a micellar structure. 
     
     
         11 . The dsRNA of  claim 10 , wherein the micellar structure comprises a liposome. 
     
     
         12 . The dsRNA of  claim 1 , wherein the target gene is expressed in eukaryotic cells. 
     
     
         13 . The dsRNA of  claim 1 , wherein the ends of the dsRNA are modified in order for the double-stranded structure to counteract degradation. 
     
     
         14 . The dsRNA of  claim 1 , wherein at least two dsRNAs which differ from each other are introduced into the cell.

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