IP Library Granted Patent US 8,952,145
Granted Patent B2
US 8,952,145 · App. 13/789,368 · Granted Feb 10, 2015

Compositions and their uses directed to huntingtin

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Quick Facts
Patent No.
US 8,952,145
App. No.
13/789,368
Granted
Feb 10, 2015
Kind
B2
Abstract

Disclosed herein are compounds, compositions and methods for modulating the expression of huntingtin in a cell, tissue or animal. Further provided are methods of slowing or preventing Huntington's Disease (HD) progression using an antisense compound targeted to huntingtin. Additionally provided are methods of delaying or preventing the onset of Huntington's Disease (HD) in an individual susceptible to Huntington's Disease (HD). Also provided are uses of disclosed compounds and compositions in the manufacture of a medicament for treatment of diseases and disorders.

Claims (20)

1. An antisense oligonucleotide 12 to 35 nucleotides in length comprising at least 12 consecutive nucleotides having at least 90% complementarity to nucleotides 4856-4894 of SEQ ID NO: 4, wherein the antisense oligonucleotide has a gap segment positioned between 5′ and 3′ wing segments.

2. The antisense oligonucleotide of claim 1 , wherein said antisense oligonucleotide comprises at least 12 consecutive nucleotides having at least 95% complementarity to nucleotides 4856-4894 of SEQ ID NO: 4.

3. The antisense oligonucleotide of claim 1 , wherein said antisense oligonucleotide comprises at least 12 consecutive nucleotides having 100% complementarity to nucleotides 4856-4894 of SEQ ID NO: 4.

4. The antisense oligonucleotide of claim 1 having at least one modified internucleoside linkage, sugar moiety, or nucleobase.

5. The antisense oligonucleotide of claim 1 , wherein the gap segment of the chimeric oligonucleotide is comprised of 2′-deoxynucleotides and the wing segments are comprised of nucleotides having modified sugar moieties.

6. The antisense oligonucleotide of claim 5 , wherein the modified sugar moiety is 2′-OMe or a bicyclic nucleic acid.

7. The antisense oligonucleotide of claim 1 , wherein the gap segment of the chimeric oligonucleotide consists of ten 2′-deoxynucleotides and each wing segment consists of five 2′-O-methoxyethyl-modified nucleotides.

8. The antisense oligonucleotide of claim 7 , wherein said antisense oligonucleotide is 20 nucleotides in length.

9. The antisense oligonucleotide of claim 1 , wherein each internucleoside linkage is a phosphorothioate internucleoside linkage.

10. The antisense oligonucleotide of claim 1 , wherein the each cytosine is a 5-methylcytosine.

11. The antisense oligonucleotide of claim 1 , wherein said oligonucleotide is 17 to 25 nucleotides in length.

12. The antisense oligonucleotide of claim 1 , wherein said oligonucleotide is 19 to 23 nucleotides in length.

13. The antisense oligonucleotide of claim 1 , wherein said oligonucleotide is 20 nucleotides in length.

14. A pharmaceutical composition comprising an antisense oligonucleotide of claim 1 and a pharmaceutically acceptable diluent.

15. The antisense oligonucleotide of claim 1 , which is 17 to 25 nucleotides in length.

16. The antisense oligonucleotide of claim 15 , which has at least 95% complementarity to nucleotides 4856-4894 of SEQ ID NO: 4.

17. The antisense oligonucleotide of claim 15 , which has 100% complementarity to nucleotides 4856-4894 of SEQ ID NO: 4.

18. The antisense oligonucleotide of claim 1 , which is 19 to 23 nucleotides in length.

19. The antisense oligonucleotide of claim 18 , which has at least 95% complementarity to nucleotides 4856-4894 of SEQ ID NO: 4.

20. The antisense oligonucleotide of claim 18 , which has 100% complementarity to nucleotides 4856-4894 of SEQ ID NO: 4.

Assignments (1)
CHANGE OF NAME Recorded Jun 15, 2017
From: ISIS PHARMACEUTICALS, INC.
To: IONIS PHARMACEUTICALS, INC.
Reel/Frame 042822/0152 →