Compositions and methods for inhibiting expression of RRM2 genes

US11920134B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-11920134-B2
Application numberUS-202016846535-A
CountryUS
Kind codeB2
Filing dateApr 13, 2020
Priority dateOct 18, 2010
Publication dateMar 5, 2024
Grant dateMar 5, 2024

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  1. Title

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  2. Abstract

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  5. First independent claim

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Abstract

Official abstract text for this publication.

The invention relates to a double-stranded ribonucleic acid (dsRNA) for inhibiting the expression of a RRM2 gene. The invention also relates to a pharmaceutical composition comprising the dsRNA or nucleic acid molecules or vectors encoding the same together with a pharmaceutically acceptable carrier; methods for treating diseases caused by the expression of a RRM2 gene using said pharmaceutical composition; and methods for inhibiting the expression of RRM2 in a cell.

First claim

Opening claim text (preview).

We claim: 1. A double-stranded ribonucleic acid molecule for inhibiting the expression of a ribonucleotide reductase M2 (RRM2) gene, wherein the double-stranded ribonucleic acid molecule comprises a sense strand and an antisense strand, wherein the antisense strand and the sense strand are each less than about 30 nucleotides in length, wherein the antisense strand comprises the nucleotide sequence of any of SEQ ID NO: 259, 279, 307, 309, 314, 333, 344, 363 or 395, wherein the sense strand is at least substantially complementary to the antisense strand, and wherein the sense strand and/or the antisense strand comprises at least one modified nucleotide. 2. The double-stranded ribonucleic acid molecule of claim 1 , wherein the antisense strand and the sense strand are each 19-24 nucleotides in length. 3. The double-stranded ribonucleic acid molecule of claim 2 , wherein the modified nucleotide is selected from the group consisting of: 2′-O-methyl modified nucleotide, nucleotide comprising a 5′-phosphorothioate group, 2′-deoxy-2′-fluoro modified nucleotide, 2′-deoxy-modified nucleotide, locked nucleotide, abasic nucleotide, inverted deoxythymidine, 2′-amino-modified nucleotide, 2′-alkyl-modified nucleotide, morpholino nucleotide, phosphoramidate, and non-natural base comprising nucleotide. 4. The double-stranded ribonucleic acid molecule of claim 2 , wherein the sense strand and the antisense strand each comprise at least one modified nucleotide. 5. The double-stranded ribonucleic acid molecule of claim 4 , wherein the modified nucleotide in the sense strand and the modified nucleotide in the antisense strand is independently selected from the group consisting of: 2′-O-methyl modified nucleotide, nucleotide comprising a 5′-phosphorothioate group, 2′-deoxy-2′-fluoro modified nucleotide, 2′-deoxy-modified nucleotide, locked nucleotide, abasic nucleotide, inverted deoxythymidine, 2′-amino-modified nucleotide, 2′-alkyl-modified nucleotide, morpholino nucleotide, phosphoramidate, and non-natural base comprising nucleotide. 6. The double-stranded ribonucleic acid molecule of claim 1 , wherein the sense strand comprises the nucleotide sequence of any of SEQ ID NO: NO:26, 46, 74, 76, 81, 100, 111, 130 or 163. 7. The double-stranded ribonucleic acid molecule of claim 6 , wherein the sense strand and/or the antisense strand further comprises a 3′ overhang of 1-5 nucleotides in length. 8. The double-stranded ribonucleic acid molecule of claim 7 , wherein the 3′ overhang comprises nucleotides linked by one or more phosphorothioate groups. 9. The double-stranded ribonucleic acid molecule of claim 8 , wherein the 3′ overhang comprises uracil. 10. The double-stranded ribonucleic acid molecule of claim 1 , wherein the antisense strand of the double-stranded ribonucleic acid molecule comprises at least one 2′-O-methyl modified nucleotide, at least one 2′-deoxy-2′-fluoro modified nucleotide, and at least one nucleotide comprising a 5′-phosphorothioate group. 11. The double-stranded ribonucleic acid molecule of claim 1 , wherein the sense strand of the double-stranded ribonucleic acid molecule comprises at least one 2′-O-methyl modified nucleotide, at least one 2′-deoxy-2′-fluoro modified nucleotide, and at least one nucleotide comprising a 5′-phosphorothioate group. 12. The double-stranded ribonucleic acid molecule of claim 6 , wherein the sense strand and the antisense strand of the double-stranded ribonucleic acid molecule each comprises at least one 2′-O-methyl modified nucleotide, at least one 2′-deoxy-2′-fluoro modified nucleotide, and at least one nucleotide comprising a 5′-phosphorothioate group. 13. The double-stranded ribonucleic acid molecule of claim 1 , wherein the double-stranded ribonucleotic acid molecule is conjugated to a ligand. 14. The double-stranded ribonucleic acid molecule of claim 6 , wherein said double-stranded ribonucleotic acid molecule is conjugated to a ligand. 15. The double stranded ribonucleic acid molecule of claim 1 , wherein the antisense strand comprises any of SEQ ID NO:866, 738, 718, 878, 724, 781, 945, 825, 843 or 809. 16. The double stranded ribonucleic acid molecule of claim 6 , wherein the sense strand comprises any of SEQ ID NO:494, 515, 544, 546, 551, 571, 582, 601 or 634. 17. The double stranded ribonucleic acid molecule of claim 6 , wherein the antisense strand comprises any of SEQ ID NO:866, 738, 718, 878, 724, 781, 945, 825, 843 or 809, and wherein the sense strand comprises any of SEQ ID NO:494, 515, 544, 546, 551, 571, 582, 601 or 634. 18. The double-stranded ribonucleic acid molecule of claim 15 , wherein the double-stranded ribonucleotic acid molecule is conjugated to a ligand. 19. The double-stranded ribonucleic acid molecule of claim 17 , wherein the double-stranded ribonucleotic acid molecule is conjugated to a ligand. 20. A pharmaceutical composition comprising: (i) the double-stranded ribonucleic acid molecule of claim 1 , and (ii) a pharmaceutically acceptable carrier. 21. A pharmaceutical composition comprising: (i) the double-stranded ribonucleic acid molecule of claim 6 , and (ii) a pharmaceutically acceptable carrier.

Assignees

Inventors

Classifications

  • against enzymes (viral enzymes C12N15/1131; receptors C12N15/1138) · CPC title

  • Rearing or breeding animals, not otherwise provided for; New or modified breeds of animals · CPC title

  • acting on CH or CH2 groups (1.17) · CPC title

  • against oncogenes or tumor suppressor genes · CPC title

  • Ribonucleoside-diphosphate reductase (1.17.4.1) · CPC title

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What does patent US11920134B2 cover?
The invention relates to a double-stranded ribonucleic acid (dsRNA) for inhibiting the expression of a RRM2 gene. The invention also relates to a pharmaceutical composition comprising the dsRNA or nucleic acid molecules or vectors encoding the same together with a pharmaceutically acceptable carrier; methods for treating diseases caused by the expression of a RRM2 gene using said pharmaceutical…
Who is the assignee on this patent?
Arrowhead Pharmaceuticals Inc
What technology area does this patent fall under?
Primary CPC classification C12N15/1137. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Tue Mar 05 2024 00:00:00 GMT+0000 (Coordinated Universal Time) (B2). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 8 related publications on this page (citations in our corpus or others sharing the same primary CPC).