IP Library Granted Patent US 8,900,552
Granted Patent B2
US 8,900,552 · App. 13/593,148 · Granted Dec 2, 2014

Treatment of glycogen storage disease type II

Inventor: Yuan-Tsong Chen (Chapel Hill, NC)
Assignee: Duke University
A61K38/47A61K38/00
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Quick Facts
Patent No.
US 8,900,552
App. No.
13/593,148
Granted
Dec 2, 2014
Kind
B2
Abstract

Methods of treating glycogen storage disease type II, by administering acid α-glucosidase, are described, as are compositions for use in treatment of glycogen storage disease type II.

Claims (15)

1. A method of treating glycogen storage disease type II in a human in need of such treatment comprising:

i) determining if said human is cross-reactive-immunological-material positive for endogenous acid α-glucosidase (CRIM-positive), and

ii) to a human determined in step (i) to be CRIM-positive, administering recombinant human acid α-glucosidase from Chinese hamster ovary cell culture (CHO GAA) in an amount sufficient to effect said treatment.

2. A method of treating glycogen storage disease type II in a CRIM-positive human in need of such treatment comprising administering CHO GAA to the CRIM-positive human in an amount sufficient to effect said treatment.

3. The method according to claim 1 or 2 , wherein the glycogen storage disease type II is infantile glycogen storage disease type II, juvenile glycogen storage disease type II, or adult-onset glycogen storage disease type II.

4. The method according to claim 3 , wherein the glycogen storage disease type II is infantile glycogen storage disease type II.

5. The method according to claim 1 or 2 , wherein less than 15 mg of said CHO GAA per kilogram of body weight is administered.

6. The method according to claim 4 , wherein 1 to 10 mg of said CHO GAA per kilogram of body weight is administered.

7. The method according to claim 1 or 2 , wherein said CHO GAA is the precursor form of human GAA.

8. The method according to claim 1 or 2 , wherein said CHO GAA is administered at a regular interval.

9. The method according to claim 8 , wherein said CHO GAA is administered monthly, bimonthly, weekly, twice weekly or daily.

10. The method according to claim 9 wherein said CHO GAA is administered bimonthly.

11. The method according to claim 1 or 2 , wherein said CHO GAA is administered intravenously, intramuscularly, intrathecally or intraventricularly.

12. The method according to claim 1 or 2 , wherein said method comprises treating cardiomyopathy associated with glycogen storage disease type II in a human in need of such treatment.

13. A method of treating glycogen storage disease type II in a CRIM-positive human in need of such treatment comprising administering CHO GAA bimonthly to the human in an amount sufficient to effect said treatment, wherein said CHO GAA is the precursor form of human GAA.

Assignments (3)
MPEP 323.01(C) SUBMISSION Recorded Sep 9, 2021
From: DUKE UNIVERSITY
To: DUKE UNIVERSITY
Reel/Frame 057476/0541 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 9, 2021
From: DUKE UNIVERSITY
To: SYNPAC (NORTH CAROLINA), INC.
Reel/Frame 056816/0524 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 28, 2014
From: CHEN, YUAN-TSONG
To: DUKE UNIVERSITY
Reel/Frame 034051/0970 →
Continuity (7)
Continuation 13064556 · Mar 30, 2011
Continuation 12604267 · Oct 22, 2009
Continuation 11889457 · Aug 13, 2007
Continuation 11039281 · Jan 20, 2005
Continuation 09902461 · Jul 10, 2001
Provisional Application 60219237 · Jul 8, 2000
Related Publication 20130195834A1 · Aug 1, 2013