IP Library Granted Patent US 11,058,709
Granted Patent B1
US 11,058,709 · App. 15/781,249 · Granted Jul 13, 2021

Methods of treating breast cancer

Inventors: David L. Spector (Cold Spring Harbor, NY); Sarah Daniela Diermeier (Centerport, NY); Frank Rigo (Carlsbad, CA); C. Frank Bennett (Carlsbad, CA); Susan M. Freier (San Diego, CA); Gayatri Arun (Huntington, NY); Kung-Chi Chang (Cold Spring Harbor, NY)
Assignees: Ionis Pharmaceuticals, Inc.; Cold Spring Harbor Laboratory
A61K31/713A61K31/175A61K31/712A61K31/7125A61P35/00C07H21/04C12N15/113A61K2300/00
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 11,058,709
App. No.
15/781,249
Granted
Jul 13, 2021
Kind
B1
Abstract

Provided herein are methods, compounds, and compositions for reducing expression of a MaTAR in an animal. Such methods, compounds, and compositions are useful to treat, prevent, delay, or ameliorate breast cancer in an individual in need.

Claims (23)

1. A method of treating breast cancer in an animal comprising administering a therapeutically effective amount of a compound comprising a modified oligonucleotide 12 to 30 linked nucleosides in length and having a nucleobase sequence that is at least 90% complementary to a mammary tumor associated RNA (MaTAR) to the animal, thereby treating breast cancer in the animal.

2. The method of claim 1 , wherein the MaTAR is selected from a group consisting of MaTAR 1-111 and 193-280.

3. The method of claim 1 , wherein the animal is a human.

4. The method of claim 1 , wherein the modified oligonucleotide has a nucleobase sequence that is at least 90% complementary, at least 95% complementary, or 100% complementary to an equal length portion of a nucleobase sequence selected from SEQ ID NOs: 1-111 and 193-280.

5. The method of claim 1 , wherein the modified oligonucleotide is single-stranded.

6. The method of claim 1 , wherein the modified oligonucleotide is double-stranded.

7. The method of claim 1 , wherein the modified oligonucleotide comprises at least one modified internucleoside linkage, at least one modified sugar moiety, or at least one modified nucleobase.

8. The method of claim 7 , wherein the at least one modified internucleoside linkage of the modified oligonucleotide is a phosphorothioate internucleoside linkage.

9. The method of claim 7 , wherein the at least one modified sugar is a bicyclic sugar or 2′-O-methyoxyethyl.

10. The method of claim 7 , wherein the at least one modified nucleobase is a 5-methylcytosine.

11. The method of claim 9 , wherein bicyclic sugar comprises a 4′-CH(CH 3 )—O-2′ bridge or a 4′-(CH 2 ) n —O-2′ bridge, wherein n is 1 or 2.

12. The method of claim 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 linked nucleosides,

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

13. The method of claim 1 , wherein the modified oligonucleotide comprises a portion of at least 8 contiguous nucleobases of a nucleobase sequence selected from SEQ ID NOs: 112-156 and 169-192.

14. The method of claim 13 , wherein the modified oligonucleotide consists of 20 linked nucleosides and has a nucleobase sequence consisting of the nucleobase sequence of SEQ ID NO: 151.

15. The method of claim 14 , wherein the modified oligonucleotide comprises:

a gap segment consisting of ten linked deoxynucleosides;

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

a 3′ wing segment consisting five linked nucleosides,

wherein the gap segment is positioned immediately adjacent to and between the 5′ wing segment and the 3′ wing segment, wherein each nucleoside of each wing segment comprises a 2′-O-methyoxyethyl sugar modification, wherein each internucleoside linkage is a phosphorothioate linkage, and wherein each cytosine is 5-methylcytosine.

Assignments (1)
CONFIRMATORY LICENSE Recorded Jul 5, 2018
From: COLD SPRING HARBOR LABORATORY
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 046499/0130 →
Continuity (2)
Provisional Application 62378125 · Aug 22, 2016
Provisional Application 62263484 · Dec 4, 2015
Cited By (2)
US 12,319,913 US 12,371,693