IP Library Granted Patent US 9,827,295
Granted Patent B2
US 9,827,295 · App. 14/889,750 · Granted Nov 28, 2017

Methods to treat mucopolysaccharide type I or deficiency in alpha-L-iduronidase using a recombinant adeno-associated virus encoding alpha-L-iduronidase

Inventors: R. Scott McIvor (St. Louis Park, MN); Lalitha R. Belur (St. Paul, MN); Walter Low (Shorewood, MN); Carolyn Fairbanks (St. Paul, MN); Karen Kozarsky (Bala Cynwyd, PA)
Assignees: Regents of the University of Minnesota; REGENXBIO Inc.
A61K38/47C12N7/00C12N15/86A61K48/00C12N2750/14143C12N2750/14171C12N2830/007C12Y302/01076
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Quick Facts
Patent No.
US 9,827,295
App. No.
14/889,750
Granted
Nov 28, 2017
Kind
B2
Abstract

A method to prevent, inhibit or treat one or more symptoms associated with a disease of the central nervous system by intrathecally, intracerebroventricularly or endovascularly administering a rAAV encoding a gene product associated with the disease, e.g., a mammal in which the gene product is absent or present at a reduced level relative to a mammal without the disease.

Claims (30)

1. A method to inhibit or treat one or more symptoms of mucopolysaccharide type I (MPSI) in a mammal in need thereof, comprising:

administering to a cisterna magna of the mammal in need thereof a composition comprising an amount of a recombinant adeno-associated virus (rAAV) 9 or rAAVrh10vector comprising an open reading frame encoding alpha-L-iduronidase effective to inhibit or treat the one or more symptoms of MPSI.

2. The method of claim 1 wherein the mammal is an immunocompetent adult.

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

4. The method of claim 1 wherein neurodegeneration is inhibited or treated by the administration.

5. The method of claim 1 wherein prior to administration of the composition the mammal is immunotolerized to alpha-L-iduronidase.

6. The method of claim 1 wherein the amount administered reduces glycosaminoglycans (GAG).

7. The method of claim 1 wherein rAAV9 vector is administered.

8. The method of claim 1 wherein rAAVrh10 vector is administered.

9. A method to inhibit or treat one or more symptoms of mucopolysaccharidosis type I (MPSI) in a mammal in need thereof, comprising:

administering to the mammal in need thereof an immune suppressant, and to a cisterna magna of the mammal a composition comprising an amount of a rAAV9 or rAAVrh10 vector comprising an open reading frame encoding alpha-L-iduronidase effective to inhibit or treat the one or more symptoms of MPSI.

10. The method of claim 9 wherein the immune suppressant comprises cyclophosphamide.

11. The method of claim 9 wherein the immune suppressant comprises a glucocorticoid, cytostatic agents including an alkylating agent, an anti-metabolite, a cytotoxic antibiotic, an antibody, or an agent active on immunophilin.

12. The method of claim 9 wherein the immune suppressant comprises a nitrogen mustard, nitrosourea, platinum compound, methotrexate, azathioprine, mercaptopurine, fluorouracil, dactinomycin, an anthracyclin e, mitomycin C, bleomycin, mithramycin, IL-2 receptor-(CD25-) or CD3-directed antibodies, anti-IL-2 antibodies, ciclosporin, tacrolimus, sirolimus, IFN-β, IFN-γ, an opioid, or TNF-α (tumor necrosis factor-alpha) binding agent.

13. The method of claim 9 wherein the rAAV vector and the immune suppressant are co-administered or the immune suppressant is administered after the rAAV vector.

14. The method of claim 9 wherein the rAAV vector is a rAAV-9 vector.

15. The method of claim 9 wherein multiple doses of the composition comprising the rAAV9 or rAAVrh10 vector are administered.

16. The method of claim 9 wherein the rAAV vector is rAAVrh10 vector.

17. The method of claim 9 wherein the immune suppressant is administered before the rAAV9 or rAAVrh10 vector.

18. The method of claim 9 wherein the immune suppressant is systemically administered.

19. The method of claim 9 wherein the mammal is a human.

20. The method of claim 9 wherein the amount administered reduces glycosaminoglycans (GAG).

21. A method to inhibit or treat one or more symptoms associated with a deficiency in alpha-L-iduronidase (IDUA) in a mammal, comprising:

providing a mammal with a deficiency in alpha-L-iduronidase that is immunotolerized to alpha-L-iduronidase ; and

administering to a cisterna magna of the mammal a composition comprising an amount of a rAAV9 or rAAVrh10 vector comprising an open reading frame encoding alpha-L-iduronidase effective to inhibit or treat the one or more symptoms associated with the deficiency in alpha-L-iduronidase.

22. The method of claim 21 wherein multiple doses of the composition comprising the rAAV9 or rAAVrh10 vector are administered.

23. The method of claim 21 wherein rAAV9 vector is administered.

24. The method of claim 21 wherein rAAVrh10 vector is administered.

25. The method of claim 21 wherein the mammal is a human.

26. The method of claim 21 wherein the amount administered reduces glycosaminoglycans (GAG).

Assignments (5)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 7, 2025
From: REGENXBIO INC.
To: REGENXBIO RS LLC
Reel/Frame 071840/0471 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 26, 2017
From: LOW, WALTER
To: REGENTS OF THE UNIVERSITY OF MINNESOTA
Reel/Frame 043704/0216 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 26, 2017
From: KOZARSKY, KAREN, PH.D
To: REGENXBIO INC.
Reel/Frame 043704/0411 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 26, 2016
From: MCIVOR, R. SCOTT; BELUR, LALITHA R.; FAIRBANKS, CAROLYN
To: REGENTS OF THE UNIVERSITY OF MINNESOTA
Reel/Frame 038377/0772 →
CONFIRMATORY LICENSE Recorded Dec 7, 2015
From: UNIVERSITY OF MINNESOTA
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 037226/0098 →
Continuity (2)
Provisional Application 61823757 · May 15, 2013
Related Publication 20160120960A1 · May 5, 2016