IP Library Granted Patent US 10,245,304
Granted Patent B2
US 10,245,304 · App. 15/350,785 · Granted Apr 2, 2019

Treatment of alpha-galactosidase a deficiency

Inventors: Douglas A. Treco (Arlington, MA); Kenneth Loveday (Brookline, MA); Marianne Borowski (Glen, NH)
Assignee: SHIRE HUMAN GENETIC THERAPIES, INC.
A61K38/47A61K38/00C12Q1/54C12Y302/01022G01N2400/10
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Quick Facts
Patent No.
US 10,245,304
App. No.
15/350,785
Granted
Apr 2, 2019
Kind
B2
Abstract

The invention provides methods of treating α-galactosidase A deficiency. Dosage forms, methods of administration, and methods of analyzing human α-galactosidase A are also included.

Claims (32)

1. A kit for the treatment of α-Gal A deficiency, comprising: (a) a human α-Gal A glycoprotein preparation; and (b) instructions to administer the preparation to a subject in need thereof, wherein the serum clearance of the α-Gal A preparation from subject's circulation is less than 4 mL/min/kg on the linear portion of the AUC vs. dose curve, wherein the α-Gal A glycoprotein preparation has the following four characteristics:

(1) has less than 35% tri- and tetra-sialylated glycans combined;

(2) has greater than 50% complex glycans;

(3) has less than 45% phosphorylated glycans; and

(4) has a ratio of sialylated glycans to phosphorylated glycans greater than 1.

2. The kit of claim 1 , wherein the serum clearance of the α-Gal A preparation from subject's circulation is 3.5 mL/min/kg or less on the linear portion of the AUC vs. dose curve.

3. The kit of claim 1 , wherein the serum clearance of the α-Gal A preparation from subject's circulation is 3.0 mL/min/kg or less on the linear portion of the AUC vs. dose curve.

4. The kit of claim 1 , further comprising instructions to administer a unit dose of the α-Gal A preparation of between 0.05 mg and 2.0 mg per kilogram of body weight.

5. The kit of claim 4 , wherein the instructions to administer the unit dose of the α-Gal A preparation specify that the unit dose is between 0.05 mg and 1.0 mg per kilogram of body weight.

6. The kit of claim 4 , wherein the instructions to administer the unit dose of the α-Gal A preparation specify that the unit dose is between 0.05 mg and 0.5 mg per kilogram of body weight.

7. The kit of claim 4 , further comprising instructions to administer the unit dose no more than once every 8 weeks.

8. The kit of claim 4 , further comprising instructions to administer the unit dose no more than once every 6 weeks.

9. The kit of claim 4 , further comprising instructions to administer the unit dose no more than once every 4 weeks.

10. A kit for the treatment of α-Gal A deficiency, comprising: a human α-Gal A glycoprotein preparation and instructions to administer the preparation to a subject in need thereof at a unit dose of less than 1.0 mg per kilogram of body weight of the subject, wherein the α-Gal A glycoprotein preparation has the following four characteristics:

(1) has less than 35% tri- and tetra-sialylated glycans combined;

(2) has greater than 50% complex glycans;

(3) has less than 45% phosphorylated glycans; and

(4) has a ratio of sialylated glycans to phosphorylated glycans greater than 1.

11. The kit of claim 10 , wherein the instructions to administer the unit dose specify that the unit dose is less than 0.5 mg per kilogram of body weight of the subject.

12. The kit of claim 10 , further comprising instructions to administer the unit dose no more than once every 8 weeks.

13. The kit of claim 12 , wherein the kit comprises instructions to administer the unit dose no more than once every 6 weeks.

14. The kit of claim 12 , wherein the kit comprises instructions to administer the unit dose no more than once every 4 weeks.

15. A kit for the treatment of α-Gal A deficiency, comprising a human α-Gal A glycoprotein preparation and instructions to administer the preparation to a subject in need thereof no more than once every 8 weeks, wherein the α-Gal A glycoprotein preparation has the following four characteristics:

(1) has less than 35% tri- and tetra-sialylated glycans combined;

(2) has greater than 50% complex glycans;

(3) has less than 45% phosphorylated glycans; and

(4) has a ratio of sialylated glycans to phosphorylated glycans greater than 1.

16. The kit of claim 15 , wherein the instructions comprise instructions to administer the preparation to a subject in need thereof no more than once every 6 weeks.

17. The kit of claim 15 , wherein the instructions comprise instructions to administer the preparation to a subject in need thereof no more than once every 4 weeks.

18. The kit of claim 15 , further comprising instructions to administer a unit dose of the α-Gal A preparation of between 0.05 mg and 2.0 mg per kilogram of body weight.

19. The kit of claim 18 , wherein the instructions to administer the unit dose of the α-Gal A preparation specify that the unit dose is between 0.05 and 1.0 mg per kilogram of body weight.

20. The kit of claim 18 , wherein the instructions to administer the unit dose of the α-Gal A preparation specify that the unit dose is between 0.05 and 0.5 mg per kilogram of body weight.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 30, 2021
From: SHIRE HUMAN GENETIC THERAPIES, INC.
To: TAKEDA PHARMACEUTICAL COMPANY LIMITED
Reel/Frame 055766/0572 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 2, 2017
From: TRECO, DOUGLAS A.; LOVEDAY, KENNETH; BOROWSKI, MARIANNE
To: SHIRE HUMAN GENETIC THERAPIES, INC.
Reel/Frame 041154/0311 →
Continuity (6)
Continuation 14995540 · Jan 14, 2016
Continuation 12761287 · Apr 15, 2010
Continuation 11403618 · Apr 13, 2006
Division 10423225 · Apr 25, 2003
Provisional Application 60375584 · Apr 25, 2002
Related Publication 20170216411A1 · Aug 3, 2017