IP Library › Granted Patent US 10,603,361
Granted Patent B2
US 10,603,361 · App. 15/544,063 · Granted Mar 31, 2020

Methods of treating a subject with an alkaline phosphatase deficiency

Inventor: Tatjana Odrljin (Brookline, MA)
Assignee: Alexion Pharmaceuticals, Inc.
A61K38/465A61K31/137A61K38/46A61K45/06A61P3/00C12Y301/03001
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Quick Facts
Patent No.
US 10,603,361
App. No.
15/544,063
Granted
Mar 31, 2020
Kind
B2
Abstract

Disclosed herein are methods for treating a subject with an alkaline phosphatase deficiency, further comprising monitoring additional anaiytes, e.g., calcium, parathyroid hormone and/or vitamin D, with treatment modifications as indicated by the levels, e.g., serum levels, of the additional anaiytes.

Claims (22)

1. A method of maintaining calcium homeostasis in a subject treated with an alkaline phosphatase for an alkaline phosphatase deficiency, wherein the alkaline phosphatase is asfotase alfa comprising the amino acid sequence of SEQ ID NO: 1, wherein the subject is determined to have a serum calcium concentration of less than 8.5 mg/dL comprising administering to the subject a therapeutic agent that increases the serum calcium concentration in the subject to 8.5 mg/dL or higher.

2. The method of claim 1 , wherein the alkaline phosphatase deficiency is hypophosphatasia.

3. The method of claim 1 , wherein the alkaline phosphatase is a tissue non-specific alkaline phosphatase, a placental alkaline phosphatase, an intestinal alkaline phosphatase, an engineered alkaline phosphatase, a fusion protein comprising an alkaline phosphatase moiety, or a chimeric alkaline phosphatase.

4. The method of claim 1 , wherein, following administration of the therapeutic agent, the subject is determined to have a serum calcium concentration of higher than 10.5 mg/dL, and the method further comprises administering an additional therapeutic agent that reduces the serum calcium concentration in the subject to 10.5 mg/dL or lower.

5. The method of claim 1 , wherein the method further comprises administering calcium or vitamin D to the subject, wherein the subject has a statistically significant low serum concentration of parathyroid hormone.

6. The method of claim 1 , wherein the method further comprises administering vitamin D or a functional analog thereof to the subject, wherein the subject has a statistically significant low serum concentration of vitamin D.

7. The method of claim 2 , further comprising administering vitamin D to the subject.

8. The method of claim 7 , wherein the vitamin D is administered orally, intramuscularly, or intravenously.

9. The method of claim 1 , wherein the alkaline phosphatase is administered in a dosage of from about 2 mg/kg/week to 9 mg/kg/week, or a comparable daily dosage.

10. The method of claim 1 , wherein the therapeutic agent is calcium gluconate, or calcium chloride.

11. The method of claim 1 , wherein the therapeutic agent is vitamin D or a functional vitamin D analog.

12. The method of claim 1 , wherein the therapeutic agent is parathyroid hormone (PTH) or a functional PTH analog.

13. The method of claim 4 , wherein the third therapeutic agent is wherein the therapeutic agent is a calcimimetic.

14. The method of claim 13 , wherein the calcimimetic is cinacalcet.

15. The method of claim 4 , wherein the additional therapeutic agent is a bisphosphonate.

16. The method of claim 4 , wherein the additional therapeutic agent is prednisone.

17. The method of claim 4 , wherein the additional therapeutic agent is an intravenous fluid.

18. The method of claim 4 , wherein the additional therapeutic agent is a diuretic.

19. The method of claim 2 , further comprising administering vitamin K to the subject.

20. The method of claim 2 , further comprising administering vitamin B to the subject.

21. The method of claim 2 , further comprising administering a multivitamin to the subject.

22. The method of claim 1 , wherein the subject has a serum calcium concentration of 7.0 mg/dL or lower to 0.5 mg/dL or lower.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 5, 2017
From: ODRLJIN, TATJANA
To: ALEXION PHARMACEUTICALS, INC.
Reel/Frame 043796/0967 →
Continuity (2)
Provisional Application 62108669 · Jan 28, 2015
Related Publication 20180333470A1 · Nov 22, 2018
Cited By (7)
US 12,268,733 US 12,318,434 US 12,433,938 US 12,472,147 US 12,611,447 US 12,648,987 US 12,691,077