IP Library Granted Patent US 10,011,651
Granted Patent B2
US 10,011,651 · App. 14/305,402 · Granted Jul 3, 2018

Methods and compositions for increasing iduronate 2-sulfatase activity in the CNS

Inventors: William M. Pardridge (Pacific Palisades, CA); Ruben J. Boado (Agoura Hills, CA)
Assignee: ARMAGEN, INC.
C07K16/18C07K16/2869C12N9/16A61K38/00C07K2317/565C07K2319/30C07K2319/33C12Y301/06013
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Quick Facts
Patent No.
US 10,011,651
App. No.
14/305,402
Granted
Jul 3, 2018
Kind
B2
Abstract

Provided herein are methods and compositions for treating a subject suffering from a deficiency in iduronate 2-sulfatase in the CNS. The methods include systemic administration of a bifunctional fusion antibody comprising an antibody that crosses the blood brain barrier (BBB) and an iduronate 2-sulfatase.

Claims (41)

1. A method for increasing iduronate-2-sulfatase (IDS) activity in a central nervous system of a subject with Hunter's syndrome in need thereof, comprising systemically administering to the subject a therapeutically effective dose of a fusion antibody having iduronate-2-sulfatase (IDS) activity, wherein the fusion antibody comprises:

(a) a fusion protein comprising amino acid sequences of an immunoglobulin heavy chain and an iduronate-2-sulfatase, wherein the amino acid sequence of the iduronate-2-sulfatase is covalently linked to a carboxy terminus of the amino acid sequence of the immunoglobulin heavy chain; and

(b) an immunoglobulin light chain;

wherein the fusion antibody crosses a blood brain barrier (BBB) and catalyzes hydrolysis of 2-sulfate groups of L-iduronate 2-sulfate units of dermatan sulfate, heparan sulfate or heparin.

2. The method of claim 1 , wherein the fusion antibody is post-translationally modified by a sulfatase modifying factor type 1 (SUMF1).

3. The method of claim 2 , wherein the fusion antibody comprises formylglycine.

4. The method of claim 1 , wherein the IDS retains at least 20% of its activity compared to its activity as a separate entity.

5. The method of claim 1 , wherein the IDS and the immunoglobulin each retains at least 20% of its activity compared to its activity as a separate entity.

6. The method of claim 1 , wherein at least about 25,000 units of iduronate-2-sulfatase activity are delivered to a brain, normalized per 50 kg body weight.

7. The method of claim 1 , wherein the therapeutically effective dose comprises at least about 250,000 units of iduronate-2-sulfatase activity or at least about 25,000 units/Kg of body weight.

8. The method of claim 1 , wherein the iduronate-2-sulfatase activity of the fusion antibody is at least 10,000 units/mg.

9. The method of claim 1 , wherein the immunoglobulin heavy chain is an immunoglobulin heavy chain of IgG.

10. The method of claim 1 , wherein the immunoglobulin heavy chain is an immunoglobulin heavy chain of kappa class.

11. The method of claim 1 , wherein the immunoglobulin light chain is an immunoglobulin light chain of IgG.

12. The method of claim 1 , wherein the immunoglobulin light chain is an immunoglobulin light chain of kappa class.

13. The method of claim 1 , wherein the fusion antibody crosses the BBB by binding an endogenous BBB receptor-mediated transport system.

14. The method of claim 1 , wherein the fusion antibody crosses the BBB via an endogenous BBB receptor selected from the group consisting of the insulin receptor, transferrin receptor, leptin receptor, lipoprotein receptor, and the IGF receptor.

15. The method of claim 1 , wherein the fusion antibody crosses the BBB by binding an insulin receptor.

16. A method for increasing iduronate-2-sulfatase (IDS) activity in a central nervous system of a subject with Hunter's syndrome in need thereof, comprising systemically administering to the subject a therapeutically effective dose of a fusion antibody having iduronate-2-sulfatase activity, wherein the fusion antibody comprises:

(a) a fusion protein comprising a amino acid sequence that is at least 95% identical to SEQ ID NO:10, and

(b) an immunoglobulin light chain;

wherein the fusion antibody crosses a blood brain barrier (BBB) and catalyzes hydrolysis of 2-sulfate groups of L-iduronate 2-sulfate units of dermatan sulfate, heparan sulfate or heparin.

17. The method of claim 16 , wherein the fusion antibody is post-translationally modified by a sulfatase modifying factor type 1 (SUMF1).

18. The method of claim 16 , wherein the fusion antibody comprises formylglycine.

19. The method of claim 16 , wherein at least about 25,000 units of iduronate-2-sulfatase activity are delivered to a brain, normalized per 50 kg body weight.

20. The method of claim 16 , wherein the therapeutically effective dose comprises at least about 250,000 units of iduronate-2-sulfatase activity or at least about 25,000 units of iduronate-2-sulfatase activity/Kg of body weight.

21. The method of claim 16 , wherein the iduronate-2-sulfatase activity of the fusion antibody is at least about 10,000 units/mg.

22. The method of claim 1 , wherein the IDS retains at least 20% of its activity compared to its activity as a separate entity.

23. The method of claim 16 , wherein the IDS and the immunoglobulin each retains at least 20% of its activity compared to its activity as a separate entity.

24. The method of claim 16 , wherein the systemic administration is parenteral, intravenous, subcutaneous, intra-muscular, trans-nasal, intra-arterial, transdermal, or respiratory.

25. The method of claim 16 , wherein the immunoglobulin light chain is an immunoglobulin light chain of IgG.

26. The method of claim 16 , wherein the immunoglobulin light chain is an immunoglobulin light chain of kappa class.

27. The method of claim 16 , wherein the fusion antibody crosses the BBB by binding an endogenous BBB receptor-mediated transport system.

28. The method of claim 16 , wherein the fusion antibody crosses the BBB via an endogenous BBB receptor selected from the group consisting of the insulin receptor, transferrin receptor, leptin receptor, lipoprotein receptor, and the IGF receptor.

29. The method of claim 16 , wherein the fusion antibody crosses the BBB by binding an insulin receptor.

30. A method for increasing iduronate-2-sulfatase (IDS) activity in a central nervous system of a subject with Hunter's syndrome in need thereof, comprising systemically administering to the subject a therapeutically effective dose of a fusion antibody having iduronate-2-sulfatase activity, wherein the fusion antibody comprises:

(a) a fusion protein comprising amino acid sequences of an immunoglobulin light chain and an iduronate-2-sulfatase, wherein the amino acid sequence of the iduronate-2-sulfatase is covalently linked to a carboxy terminus of the amino acid sequence of the immunoglobulin light chain; and

(b) an immunoglobulin heavy chain;

wherein the fusion antibody crosses a blood brain barrier (BBB) and catalyzes hydrolysis of 2-sulfate groups of L-iduronate 2-sulfate units of dermatan sulfate, heparan sulfate or heparin.

31. The method of claim 16 , wherein the fusion antibody crosses the BBB by binding a transferrin receptor.

32. The method of claim 1 , wherein the fusion antibody crosses the BBB by binding a transferrin receptor.

Assignments (5)
RELEASE OF SECURITY INTEREST Recorded Apr 11, 2020
From: JCR PHARMACEUTICALS CO., LTD.
To: ARMAGEN, INC.
Reel/Frame 052373/0585 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 18, 2019
From: OXFORD FINANCE LLC
To: JCR PHARMACEUTICALS CO., LTD.
Reel/Frame 051042/0528 →
SECURITY INTEREST Recorded Feb 2, 2018
From: ARMAGEN, INC.
To: OXFORD FINANCE LLC, AS COLLATERAL AGENT AND LENDER
Reel/Frame 044815/0135 →
CHANGE OF NAME Recorded Mar 22, 2017
From: ARMAGEN TECHNOLOGIES, INC.
To: ARMAGEN, INC.
Reel/Frame 042067/0068 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 26, 2014
From: PARDRIDGE, WILLIAM M.; BOADO, RUBEN J.
To: ARMAGEN TECHNOLOGIES, INC.
Reel/Frame 033826/0582 →
Continuity (4)
Continuation 12901481 · Oct 8, 2010
Provisional Application 61250378 · Oct 9, 2009
Provisional Application 61256049 · Oct 29, 2009
Related Publication 20150004160A1 · Jan 1, 2015