IP Library Granted Patent US 11,591,595
Granted Patent B2
US 11,591,595 · App. 16/986,770 · Granted Feb 28, 2023

Compositions for modulating Tau expression

Inventors: Holly Kordasiewicz (San Diego, CA); Eric E. Swayze (Encinitas, CA); Susan M. Freier (San Diego, CA); Huynh-Hoa Bui (San Diego, CA)
Assignee: Biogen MA Inc.
C12N15/113A61K31/711C07H21/02C12N2310/11C12N2310/315C12N2310/3341C12N2310/341C12N2310/345C12N2310/346
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Quick Facts
Patent No.
US 11,591,595
App. No.
16/986,770
Granted
Feb 28, 2023
Kind
B2
Abstract

Disclosed herein are antisense compounds and methods for decreasing Tau mRNA and protein expression. Such methods, compounds, and compositions are useful to treat, prevent, or ameliorate Tau-associated diseases, disorders, and conditions.

Claims (47)

1. A compound comprising a modified oligonucleotide according to the following formula:

Ges Teo Geo Aeo Tes Ads Tds Tds Gds Tds mCds mCds Ads Geo Geo Ges Aes mCe (nucleobase sequence of SEQ ID NO:1967); wherein

A=an adenine,

mC=a 5-methylcytosine

G=a guanine,

T=a thymine,

e=a 2′-O-methoxyethyl modified nucleoside,

d=a 2′-deoxynucleoside,

o=a phosphodiester internucleoside linkage, and

s=a phosphorothioate internucleoside linkage.

2. A composition comprising the compound of claim 1 , or salt thereof, and at least one of a pharmaceutically acceptable carrier or diluent.

3. A method of treating a tau associated disease in a human subject in need thereof, the method comprising administering to the human subject the compound of claim 1 .

4. The method of claim 3 , wherein the tau associated disease is a neurodegenerative disorder.

5. The method of claim 4 , wherein the neurodegenerative disorder is a Tauopathy, Alzheimer's Disease, Fronto-temporal Dementia (FTD), FTDP-17, Progressive Supranuclear Palsy (PSP), Chronic Traumatic Encephalopathy (CTE), Corticobasal Ganglionic Degeneration (CBD), Epilepsy, or Dravet's Syndrome.

6. A compound comprising a modified oligonucleotide consisting of 12 to 30 linked nucleosides and having a nucleobase sequence comprising at least 10 consecutive nucleobases of SEQ ID NO:1967.

7. The compound of claim 6 , comprising at least 11 consecutive nucleobases of SEQ ID NO:1967.

8. The compound of claim 6 , comprising at least 12 consecutive nucleobases of SEQ ID NO:1967.

9. The compound of claim 6 , comprising at least 13 consecutive nucleobases of SEQ ID NO:1967.

10. The compound of claim 6 , comprising at least 14 consecutive nucleobases of SEQ ID NO:1967.

11. The compound of claim 6 , comprising at least 15 consecutive nucleobases of SEQ ID NO:1967.

12. The compound of claim 6 , comprising at least 16 consecutive nucleobases of SEQ ID NO:1967.

13. The compound of claim 6 , comprising at least 17 consecutive nucleobases of SEQ ID NO:1967.

14. The compound of claim 6 , comprising at least 18 consecutive nucleobases of SEQ ID NO:1967.

15. The compound of claim 6 , consisting of a single-stranded modified oligonucleotide.

16. The compound of claim 6 , wherein at least one internucleoside linkage is a modified internucleoside linkage.

17. The compound of claim 6 , wherein at least one internucleoside linkage is a phosphorothioate linkage and at least one internucleoside linkage is a phosphodiester linkage.

18. The compound of claim 16 , wherein the modified internucleoside linkage comprises a phosphorothioate internucleoside linkage.

19. The compound of claim 6 , wherein at least one internucleoside linkage of the modified oligonucleotide comprises a phosphodiester internucleoside linkage.

20. The compound of claim 6 , wherein at least one nucleoside comprises a modified nucleobase.

21. The compound of claim 20 , wherein the modified nucleobase is a 5-methylcytosine.

22. The compound of claim 6 , wherein at least one nucleoside of the modified oligonucleotide comprises a modified sugar.

23. The compound of claim 22 , wherein the modified sugar is a bicyclic sugar.

24. The compound of claim 23 , wherein the bicyclic sugar comprises a chemical bridge between the 4′ and 2′ positions of the sugar, wherein each chemical bridge is independently selected from: 4′-CH(R)—2′ and 4′-(CH 2 ) 2 —O-2′, wherein each R is independently selected from H, C 1 -C 6 alkyl and C 1 -C 6 alkoxy.

25. The compound of claim 24 , wherein at least one chemical bridge is 4′-CH(R)—O-2′ and wherein R is methyl.

26. The compound of claim 22 , wherein the modified sugar comprises a 2′-O-methoxyethyl group.

27. The compound of claim 6 , wherein at least one nucleoside of the modified oligonucleotide comprises a sugar surrogate.

28. The compound of claim 27 , wherein the sugar surrogate is a morpholino or a peptide nucleic acid.

29. The compound of claim 6 , wherein the modified oligonucleotide consists of 18 linked nucleosides.

30. The compound of claim 6 , wherein the modified oligonucleotide comprises:

a gap segment consisting of 8 linked deoxynucleosides;

a 5′ wing segment consisting of 5 linked nucleosides; and

a 3′ wing segment consisting of 5 linked nucleosides;

wherein the gap segment is positioned between the 5′ wing segment and the 3′ wing segment and wherein each nucleoside of each wing segment comprises a modified sugar.

31. A composition comprising the compound of claim 6 or salt thereof and at least one of a pharmaceutically acceptable carrier or diluent.

32. A method of treating a tau associated disease in a human subject in need thereof, the method comprising administering to the human subject the compound of claim 6 .

33. The method of claim 32 , wherein the tau associated disease is a neurodegenerative disorder.

34. The method of claim 33 , wherein the neurodegenerative disorder is a Tauopathy, Alzheimer's Disease, Fronto-temporal Dementia (FTD), FTDP-17, Progressive Supranuclear Palsy (PSP), Chronic Traumatic Encephalopathy (CTE), Corticobasal Ganglionic Degeneration (CBD), Epilepsy, or Dravet's Syndrome.

Assignments (3)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 16, 2021
From: KORDASIEWICZ, HOLLY; SWAYZE, ERIC E.; FREIER, SUSAN M.; BUI, HUYNH-HOA
To: ISIS PHARMACEUTICALS, INC.
Reel/Frame 055607/0134 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 16, 2021
From: IONIS PHARMACEUTICALS, INC.
To: BIOGEN MA INC.
Reel/Frame 055607/0254 →
CHANGE OF NAME Recorded Mar 16, 2021
From: ISIS PHARMACEUTICALS, INC.
To: IONIS PHARMACEUTICALS, INC.
Reel/Frame 055607/0698 →
Continuity (7)
Division 15593173 · May 11, 2017
Division 14906047
Provisional Application 62014486 · Jun 19, 2014
Provisional Application 61885371 · Oct 1, 2013
Provisional Application 61879621 · Sep 18, 2013
Provisional Application 61856551 · Jul 19, 2013
Related Publication 20210071176A1 · Mar 11, 2021