IP Library Granted Patent US 9,359,609
Granted Patent B2
US 9,359,609 · App. 14/677,387 · Granted Jun 7, 2016

Methods for treatment of alport syndrome

Inventors: Jeremy Duffield (Seattle, WA); Balkrishen Bhat (San Diego, CA); Deidre MacKenna (San Diego, CA)
Assignee: Regulus Therapeutics Inc.
C12N15/113A61K31/7088A61K45/06C12N2310/113C12N2310/313C12N2310/315C12N2310/321C12N2310/3233
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Quick Facts
Patent No.
US 9,359,609
App. No.
14/677,387
Granted
Jun 7, 2016
Kind
B2
Abstract

Provided herein are methods for the treatment of Alport Syndrome, using modified oligonucleotides targeted to miR-21. In certain embodiments, a modified oligonucleotide targeted to miR-21 improves kidney function and/or reduces fibrosis in subjects having Alport Syndrome. In certain embodiments, administration of a modified oligonucleotide targeted to miR-21 delays the onset of end-stage renal disease in a subject having Alport Syndrome. In certain embodiments, a modified oligonucleotide targeted to miR-21 delays the need for dialysis or kidney transplant in a subject having Alport Syndrome.

Claims (20)

1. A method of treating Alport Syndrome comprising administering to a subject having or suspected of having Alport Syndrome a pharmaceutical composition comprising a therapeutically effective amount 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), where nucleosides not followed by a subscript are β-D-deoxyribonucleosides; nucleosides followed by a subscript “E” are 2′-MOE nucleosides; nucleosides followed by a subscript “S” are S-cEt nucleosides, and each internucleoside linkage is a phosphorothioate internucleoside linkage.

2. The method of claim 1 wherein the subject has been diagnosed as having Alport Syndrome prior to administering the pharmaceutical composition.

3. The method of claim 1 , wherein the subject is male.

4. The method of claim 1 , wherein the subject is female.

5. The method of claim 1 , wherein the Alport Syndrome is the X-linked form of Alport Syndrome.

6. The method of claim 1 , wherein the Alport Syndrome is the autosomal form of Alport Syndrome.

7. The method of claim 5 , wherein the subject is female.

8. The method of claim 5 , wherein the subject is male.

9. The method of claim 6 , wherein the subject is female.

10. The method of claim 6 , wherein the subject is male.

11. The method of claim 1 , wherein the subject has a mutation in the gene encoding the alpha 3 chain of type IV collagen.

12. The method of claim 11 , wherein the subject is female.

13. The method of claim 11 , wherein the subject is male.

14. The method of claim 1 , wherein the subject has a mutation in the gene encoding the alpha 4 chain of type IV collagen.

15. The method of claim 14 , wherein the subject is female.

16. The method of claim 14 , wherein the subject is male.

17. The method of claim 1 , wherein the subject has a mutation in the gene encoding the alpha 5 chain of type IV collagen.

18. The method of claim 17 , wherein the subject is female.

19. The method of claim 17 , wherein the subject is male.

20. The method of claim 1 , wherein the pharmaceutical composition is a sterile aqueous solution.

Assignments (4)
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 →
Continuity (4)
Continuation 14048827 · Oct 8, 2013
Provisional Application 61711514 · Oct 9, 2012
Provisional Application 61779137 · Mar 13, 2013
Related Publication 20150299704A1 · Oct 22, 2015