IP Library › Granted Patent US 11,535,849
Granted Patent B2
US 11,535,849 · App. 16/889,470 · Granted Dec 27, 2022

Modulation of transthyretin expression

Inventors: Brett P. Monia (Encinitas, CA); Susan M. Freier (San Diego, CA); Andrew M. Siwkowski (Carlsbad, CA); Shuling Guo (Carlsbad, CA)
Assignee: Ionis Pharmaceuticals, Inc.
C12N15/113A61K31/712C12N2310/11C12N2310/14C12N2310/315C12N2310/321C12N2310/3341C12N2310/341C12N2310/52C12N2320/30
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 11,535,849
App. No.
16/889,470
Granted
Dec 27, 2022
Kind
B2
Abstract

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

Claims (15)

1. A compound comprising a modified oligonucleotide consisting of 15 to 30 linked nucleosides wherein the linked nucleosides comprise at least a 15 contiguous nucleobase portion that is complementary to an equal length nucleobase portion within nucleotides 120-139 of SEQ ID NO: 1;

wherein the modified oligonucleotide comprises:

a gap segment consisting of linked deoxynucleosides;

a 5′ wing segment consisting of linked nucleosides; and

a 3′ wing segment consisting of linked nucleosides;

wherein the gap segment is positioned between the 5′ wing segment and the 3′ wing segment, and wherein at least one nucleoside comprises a modified sugar.

2. The compound of claim 1 , wherein the modified oligonucleotide has at least an 16, at least an 17, at least an 18, at least an 19, or at least a 20 contiguous nucleobase portion of which is complementary within nucleotides 120-139 of SEQ ID NO: 1.

3. The compound of claim 1 , wherein the nucleobase sequence of the modified oligonucleotide is at least 95% complementary over its entire length to a nucleobase sequence of SEQ ID NO: 1, 2, or 4.

4. The compound of claim 1 , wherein the modified oligonucleotide has at least one modified internucleoside linkage.

5. The compound of claim 4 , wherein the modified internucleoside linkage is a phosphorothioate internucleoside linkage.

6. The compound of claim 1 , wherein each nucleoside of each wing segment comprises a modified sugar.

7. The compound of claim 6 , wherein the modified sugar is a bicyclic sugar comprising a 4′-CH(CH 3 )—O-2′ bridge or the modified sugar comprises a 2′-O-methoxyethyl moiety.

8. The compound of claim 1 , wherein each nucleoside of each wing segment comprises a 2′-O-methoxyethyl sugar, wherein each internucleoside linkage is a phosphorothioate linkage, and wherein each cytosine of the modified oligonucleotide is a 5-methylcytosine.

9. A composition comprising the compound of claim 1 , or a salt thereof, and a pharmaceutically acceptable carrier or diluent.

10. A method of treating transthyretin amyloidosis in an animal comprising administering to the animal a compound comprising a modified oligonucleotide consisting of 15 to 30 linked nucleosides wherein the linked nucleosides comprise at least a 15 contiguous nucleobase portion that is complementary to an equal length nucleobase portion within nucleotides 120-139 of SEQ ID NO: 1.

Continuity (10)
Continuation 16229643 · Dec 21, 2018
Continuation 15729860 · Oct 11, 2017
Continuation 15190533 · Jun 23, 2016
Continuation 14717746 · May 20, 2015
Division 14184984 · Feb 20, 2014
Division 13944786 · Jul 17, 2013
Continuation 13098303 · Apr 29, 2011
Provisional Application 61405163 · Oct 20, 2010
Provisional Application 61329538 · Apr 29, 2010
Related Publication 20210095281A1 · Apr 1, 2021
Cited By (1)
US 12,606,826