IP Library Granted Patent US 11,421,231
Granted Patent B2
US 11,421,231 · App. 17/068,185 · Granted Aug 23, 2022

Modulation of Huntington expression

Inventors: Gene Hung (Carlsbad, CA); C. Frank Bennett (Carlsbad, CA); Susan M. Freier (San Diego, CA); Holly Kordasiewicz (San Diego, CA); Lisa Stanek (Cambridge, MA); Don W. Cleveland (Del Mar, CA); Seng H. Cheng (Natick, MA); Lamya Shihabuddin (Brighton, MA)
Assignee: Ionis Pharmaceuticals, Inc.
C12N15/113C12N2310/11C12N2310/113C12N2310/315C12N2310/321C12N2310/3341C12N2310/341C12N2310/345C12N2310/346
View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 11,421,231
App. No.
17/068,185
Granted
Aug 23, 2022
Kind
B2
Abstract

Provided herein are methods, compounds, and compositions for reducing expression of huntingtin mRNA and protein in an animal. Such methods, compounds, and compositions are useful to treat, prevent, delay, or ameliorate Huntington's disease, or a symptom thereof.

Claims (23)

1. A single-stranded modified oligonucleotide consisting of 20 linked nucleosides and having:

a gap segment consisting of ten linked deoxynucleosides;

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

a 3′ wing segment consisting of five linked nucleosides;

wherein the gap segment is positioned between the 5′ wing segment and the 3′ wing segment;

wherein each nucleoside of each wing segment comprises a 2′O-methoxyethyl sugar; and

wherein the nucleobase sequence of the oligonucleotide consists of the sequence recited in SEQ ID NO: 36,

or a pharmaceutically acceptable salt thereof.

2. The single-stranded modified oligonucleotide of claim 1 , wherein at least one nucleoside comprises a modified nucleobase.

3. The single-stranded modified oligonucleotide of claim 2 , wherein the modified nucleobase is a 5-methylcytosine.

4. The single-stranded modified oligonucleotide of claim 1 , wherein each cytosine is a 5-methylcytosine.

5. The single-stranded modified oligonucleotide of claim 1 , wherein at least one internucleoside linkage is a modified internucleoside linkage.

6. The single-stranded modified oligonucleotide of claim 1 , wherein each internucleoside linkage is a phosphorothioate internucleoside linkage.

7. The single-stranded modified oligonucleotide of claim 4 , wherein at least one internucleoside linkage is a modified internucleoside linkage.

8. The single-stranded modified oligonucleotide of claim 4 , wherein each internucleoside linkage is a phosphorothioate internucleoside linkage.

9. A composition comprising the single-stranded modified oligonucleotide or pharmaceutically acceptable salt thereof of claim 1 and at least one pharmaceutically acceptable carrier or diluent.

10. A composition comprising the single-stranded modified oligonucleotide or pharmaceutically acceptable salt thereof of claim 4 and at least one pharmaceutically acceptable carrier or diluent.

11. A composition comprising the single-stranded modified oligonucleotide or pharmaceutically acceptable salt thereof of claim 6 and at least one pharmaceutically acceptable carrier or diluent.

12. A composition comprising the single-stranded modified oligonucleotide or pharmaceutically acceptable salt thereof of claim 8 and at least one pharmaceutically acceptable carrier or diluent.

13. The single-stranded modified oligonucleotide of claim 1 , which is capable of inhibiting huntingtin expression.

14. The single-stranded modified oligonucleotide of claim 4 , which is capable of inhibiting huntingtin expression.

15. The single-stranded modified oligonucleotide of claim 6 , which is capable of inhibiting huntingtin expression.

16. The single-stranded modified oligonucleotide of claim 8 , which is capable of inhibiting huntingtin expression.

Assignments (5)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 15, 2022
From: CHENG, SENG H.; SHIHABUDDIN, LAMYA; STANEK, LISA
To: GENZYME CORPORATION
Reel/Frame 061113/0269 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 19, 2022
From: HUNG, GENE; BENNETT, C. FRANK; FREIER, SUSAN M.; KORDASIEWICZ, HOLLY; CLEVELAND, DON W.
To: ISIS PHARMACEUTICALS
Reel/Frame 060551/0052 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 19, 2022
From: CHENG, SENG H.; SHIHABUDDIN, LAMYA; STANEK, LISA
To: GENZYME CORPORATION
Reel/Frame 060551/0075 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 19, 2022
From: GENZYME CORPORATION
To: ISIS PHARMACEUTICALS, INC.
Reel/Frame 060551/0115 →
CHANGE OF NAME Recorded Jul 19, 2022
From: ISIS PHARMACEUTICALS, INC.
To: IONIS PHARMACEUTICALS, INC.
Reel/Frame 060750/0865 →