Modified RNAi agents

US9708607B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-9708607-B2
Application numberUS-201314419211-A
CountryUS
Kind codeB2
Filing dateAug 2, 2013
Priority dateAug 3, 2012
Publication dateJul 18, 2017
Grant dateJul 18, 2017

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Abstract

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One aspect of the present invention relates to double-stranded RNAi (dsRNA) duplex agent capable of inhibiting the expression of a target gene in vivo. The dsRNA duplex comprises one or more xylo modifications in one or both strand. Other aspects of the invention relates to pharmaceutical compositions comprising these dsRNA agents suitable for in vivo therapeutic use, and methods of inhibiting the expression of a target gene by administering these dsRNA agents, e.g., for the treatment of various disease conditions.

First claim

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We claim: 1. A double-stranded RNAi agent capable of inhibiting the expression of a target gene, comprising a duplex comprising a sense strand and an antisense strand, each strand having 12 to 30 nucleotides, wherein the duplex comprises at least one xylo modified moiety represented by formula (A): wherein: Y is H, alkyl or internucleotide linkage; X is halogen, substituted or unsubstituted alkoxy, substituted or unsubstituted aminoalkyl, substituted or unsubstituted alkyl; and B is a natural or non-natural nucleobase. 2. The double-stranded RNAi agent of claim 1 , wherein X is F or OMe. 3. A double-stranded RNAi agent of claim 1 , represented by formula (III): sense: 5 ′n p -N a —(XXX) i —N b —YYY—N b —(ZZZ) j —N a - n q 3′ antisense: 3 ′n p ′-N a ′—(X′X′X′) k —N b ′—Y′Y′Y′—N b ′—(Z′Z′Z′) l —N a ′- n q ′5′  (III) wherein: j, k, and 1 are each independently 0 or 1; p and q are each independently 0-6; each Na and Na′ independently represents an oligonucleotide sequence comprising 0-25 nucleotides which are either modified or unmodified or combinations thereof, each sequence comprising at least two differently modified nucleotideseach Nb and Nb′ independently represents an oligonucleotide sequence comprising 0-10 nucleotides which are either modified or unmodified or combinations thereof; each n p and n q independently represents an overhang nucleotide; and XXX, YYY, ZZZ, X′X′X′, Y′Y′Y′, and Z′Z′Z′ each independently represent one motif of three identical modifications on three consecutive nucleotides; wherein at least one of n, N, X, Y, or Z is a xylo modified of formula (A); and wherein modifications on Nb is different than the modification on Y and modifications on Nb′ is different than the modification on Y′. 4. A double-stranded RNAi capable of inhibiting the expression of a target gene, comprising a duplex comprising a sense strand and an antisense strand, each strand having 12 to 30 nucleotides, wherein the duplex comprises at least one xylo-modified or 3′-modified moiety, wherein the duplex region is 27-30 nucleotide pairs in length. 5. A double-stranded RNAi agent capable of inhibiting the expression of a target gene, comprising a duplex comprising a sense strand and an antisense strand, each strand having 12 to 30 nucleotides, wherein the duplex comprises at least one xylo-modified or 3′-modified moiety, and wherein the duplex further comprises at least one ligand. 6. The double-stranded RNAi agent of claim 5 , wherein the ligand is a one or more GalNAc derivatives attached through a bivalent or trivalent branched linker. 7. The double-stranded RNAi agent of claim 6 , wherein the ligand is 8. The double-stranded RNAi agent of claim 5 , wherein the ligand is attached to the 3′ end of the sense strand. 9. A double-stranded RNAi agent capable of inhibiting the expression of a target gene, comprising a duplex comprising a sense strand and an antisense strand, each strand having 12 to 30 nucleotides, wherein the duplex comprises at least one xylo-modified or 3′-modified moiety, and wherein the duplex further comprises at least one phosphorothioate or methylphosphonate internucleotide linkage. 10. The double-stranded RNAi agent of claim 1 , wherein the nucleotide at the 1 position of the 5′-end of the duplex in the antisense strand is selected from the group consisting of A, dA, dU, U, and dT. 11. The double-stranded RNAi agent of claim 1 , wherein the base pair at the 1 position of the 5′-end of the duplex in the antisense strand is an AU base pair. 12. The double-stranded RNAi agent of claim 3 , wherein the Y nucleotides contain a 2′-fluoro modification. 13. The double-stranded RNAi agent of claim 3 wherein the Y′ nucleotides contain a 2′-O-methyl modification. 14. A pharmaceutical composition comprising the double-stranded RNAi agent of claim 1 alone or in combination with a pharmaceutically acceptable carrier or excipient. 15. A method for inhibiting the expression of a target gene comprising the step of administering the double-stranded RNAi agent of claim 1 , in an amount sufficient to inhibit expression of the target gene. 16. The method of claim 15 , wherein the double-stranded RNAi agent is administered through subcutaneous or intravenous administration. 17. The double-stranded RNAi agent of claim 3 , further comprising at least one phosphorothioate or methylphosphonate internucleotide linkage. 18. The double-stranded RNAi agent of claim 3 , wherein the nucleotide at the 1 position of the 5′-end of the duplex in the antisense strand is selected from the group consisting of A, dA, dU, U, and dT. 19. The double-stranded RNAi agent of claim 3 , wherein the base pair at the 1 position of the 5′-end of the duplex in the antisense strand is an AU base pair. 20. The double-stranded RNAi agent of claim 4 , wherein the double-stranded RNAi agent is represented by formula (III): sense: 5 ′n p -N a —(XXX) i —N b —YYY—N b —(ZZZ) j —N a - n q 3′ antisense: 3 ′n p ′-N a ′—(X′X′X′) k —N b ′—Y′Y′Y′—N b ′—(Z′Z′Z′) l —N a ′- n q ′5′  (III) wherein: j, k, and 1 are each independently 0 or 1; p and q are each independently 0-6; each Na and Na′ independently represents an oligonucleotide sequence comprising 0-25 nucleotides which are either modified or unmodified or combinations thereof, each sequence comprising at least two differently modified nucleotideseach Nb and Nb′ independently represents an oligonucleotide sequence comprising 0-10 nucleotides which are either modified or unmodified or combinations thereof; each n p and n q independently represents an overhang nucleotide; and XXX, YYY, ZZZ, X′X′X′, Y′Y′Y′, and Z′Z′Z′ each independently represent one motif of three identical modifications on three consecutive nucleotides; wherein at least one of n, N, X, Y, or Z is a xylo modified of formula (A); and wherein modifications on Nb is different than the modification on Y and modifications on Nb′ is different than the modification on Y′. 21. The double-stranded RNAi agent of claim 4 , wherein the nucleotide at the 1 position of the 5′-end of the duplex in the antisense strand is selected from the group consisting of A, dA, dU, U, and dT. 22. The double-stranded RNAi agent of claim 4 , wherein the base pair at the 1 position of the 5′-end of the duplex in the antisense strand is an AU base pair. 23. The double-stranded RNAi agent of claim 5 , wherein the double-stranded RNAi agent is represented by formula (III): sense: 5 ′n p -N a —(XXX) i —N b —YYY—N b —(ZZZ) j —N a - n q 3′ antisense: 3 ′n p ′-N a ′—(X′X′X′) k —N b ′—Y′Y′Y′—N b ′—(Z′Z′Z′) l —N a ′- n q ′5′  (III) wherein: j, k, and 1 are each independently 0 or 1; p and q are each independently 0-6; each Na and Na′ independently represents an oligonucleotide sequence comprising 0-25 nucleotides which are either modified or unmodified or combinations thereof, each sequence comprising at least two differently modified nucleotideseach Nb and Nb′ independently represents an oligonucleotide sequence comprising 0-10 nucleotides which are either modified or unmodified or combinations thereof; each n p and n q independently represents an overhang nucleotide; and XXX, YYY, ZZZ, X′X′X′, Y′Y′Y′, and Z′Z′Z′ each independe

Assignees

Inventors

Classifications

  • Methyl · CPC title

  • 2'-O-R Modification · CPC title

  • of the backbone · CPC title

  • C12N15/113Primary

    Non-coding nucleic acids modulating the expression of genes, e.g. antisense oligonucleotides; {Antisense DNA or RNA; Triplex- forming oligonucleotides; Catalytic nucleic acids, e.g. ribozymes; Nucleic acids used in co-suppression or gene silencing (when used in plants C12N15/8218)} · CPC title

  • with ribosyl as saccharide radical · CPC title

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What does patent US9708607B2 cover?
One aspect of the present invention relates to double-stranded RNAi (dsRNA) duplex agent capable of inhibiting the expression of a target gene in vivo. The dsRNA duplex comprises one or more xylo modifications in one or both strand. Other aspects of the invention relates to pharmaceutical compositions comprising these dsRNA agents suitable for in vivo therapeutic use, and methods of inhibiting …
Who is the assignee on this patent?
Alnylam Pharmaceuticals Inc
What technology area does this patent fall under?
Primary CPC classification C12N15/113. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Tue Jul 18 2017 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).