IP Library Granted Patent US 9,181,547
Granted Patent B2
US 9,181,547 · App. 14/111,976 · Granted Nov 10, 2015

MicroRNA compounds and methods for modulating MIR-21 activity

Inventor: Balkrishen Bhat (San Diego, CA)
Assignee: Regulus Therapeutics Inc.
C12N15/113C12N2310/113C12N2310/3231C12N2310/343C12N2310/35
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Quick Facts
Patent No.
US 9,181,547
App. No.
14/111,976
Granted
Nov 10, 2015
Kind
B2
Abstract

Described herein are compositions and methods for the inhibition of miR-21 activity. The compositions have certain nucleoside modification patterns that yield potent inhibitors of miR-21 activity. The compositions may be used to inhibit miR-21, and also to treat diseases associated with abnormal expression of miR-21, such as fibrosis and cancer.

Claims (10)

1. A modified oligonucleotide consisting of 19 linked nucleosides and having the structure:

5′-A E C S ATC S AGTC S TGAU S AAGC S TA E -3′ (SEQ ID NO: 3), wherein nucleosides not followed by a subscript are β-D-deoxyribonucleosides; nucleosides followed by a subscript “E” are 2′-methoxyethyl (2′-MOE) nucleosides; and nucleosides followed by a subscript “S” are S-constrained ethyl (S-cEt) nucleosides; and wherein each internucleoside linkage is a phosphorothioate linkage.

2. A pharmaceutical composition comprising the modified oligonucleotide of claim 1 and a pharmaceutically acceptable diluent.

3. The pharmaceutical composition of claim 2 , which is a sterile aqueous solution.

4. A pharmaceutical composition consisting essentially of a modified oligonucleotide in a sterile aqueous solution, wherein the modified oligonucleotide consists of 19 linked nucleosides and has the structure:

5′-A E C S ATC S AGTC S TGAU S AAGC S TA E -3′ (SEQ ID NO: 3), wherein nucleosides not followed by a subscript are β-D-deoxyribonucleosides; nucleosides followed by a subscript “E” are 2′-methoxyethyl (2′-MOE) nucleosides; and nucleosides followed by a subscript “S” are S-constrained ethyl (S-cEt) nucleosides; and wherein each internucleoside linkage is a phosphorothioate linkage.

5. A lyophilized composition comprising a modified oligonucleotide consisting of 19 linked nucleosides and having the structure:

5′-A E C S ATC S AGTC S TGAU S AAGC S TA E -3′ (SEQ ID NO: 3), wherein nucleosides not followed by a subscript are β-D-deoxyribonucleosides; nucleosides followed by a subscript “E” are 2′-methoxyethyl (2′-MOE) nucleosides; and nucleosides followed by a subscript “S” are S-constrained ethyl (S-cEt) nucleosides; and wherein each internucleoside linkage is a phosphorothioate linkage.

6. A lyophilized composition consisting essentially of a modified oligonucleotide consisting of 19 linked nucleosides and having the structure:

5′-A E C S ATC S AGTC S TGAU S AAGC S TA E -3′ (SEQ ID NO: 3), wherein nucleosides not followed by a subscript are β-D-deoxyribonucleosides; nucleosides followed by a subscript “E” are 2′-methoxyethyl (2′-MOE) nucleosides; and nucleosides followed by a subscript “S” are S-constrained ethyl (S-cEt) nucleosides; and wherein each internucleoside linkage is a phosphorothioate linkage.

Assignments (5)
RELEASE OF SECURITY INTEREST Recorded May 14, 2024
From: OXFORD FINANCE LLC, AS COLLATERAL AGENT AND LENDER
To: REGULUS THERAPEUTICS INC.
Reel/Frame 067402/0782 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 3, 2019
From: REGULUS THERAPEUTICS INC.
To: SANOFI
Reel/Frame 049344/0688 →
RELEASE OF SECURITY INTEREST Recorded Nov 7, 2018
From: OXFORD FINANCE LLC
To: REGULUS THERAPEUTICS INC.
Reel/Frame 047445/0286 →
SECURITY INTEREST Recorded Aug 8, 2018
From: REGULUS THERAPEUTICS INC.
To: OXFORD FINANCE LLC, AS COLLATERAL AGENT AND LENDER
Reel/Frame 046748/0561 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 20, 2013
From: BHAT, BALKRISHEN
To: REGULUS THERAPEUTICS INC.
Reel/Frame 031825/0801 →
Continuity (3)
Provisional Application 61478767 · Apr 25, 2011
Provisional Application 61565779 · Dec 1, 2011
Related Publication 20140107183A1 · Apr 17, 2014