IP Library Granted Patent US 8,642,732
Granted Patent B2
US 8,642,732 · App. 13/425,583 · Granted Feb 4, 2014

Polymer-conjugated glycosylated neublastin

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Quick Facts
Patent No.
US 8,642,732
App. No.
13/425,583
Granted
Feb 4, 2014
Kind
B2
Abstract

The following class of molecule is disclosed: a dimer containing a first neublastin polypeptide and a second neublastin polypeptide, wherein: (a) at least one of the polypeptides is glycosylated; (b) at least one of the polypeptides is conjugated at its N-terminus to a water-soluble synthetic polymer; and (c) neither of the polypeptides is conjugated to a water-soluble synthetic polymer at a position other than the N-terminus. Such dimers possess the biological activity of wild-type neublastin while displaying enhanced serum half-life and enhanced potency relative to wild-type neublastin.

Claims (22)

1. A dimer comprising a first neublastin polypeptide and a second neublastin polypeptide, wherein: (a) at least one of the polypeptides is glycosylated; (b) at least one of the polypeptides is conjugated at its N-terminus to a water-soluble synthetic polymer; and (c) neither of the polypeptides is conjugated to a water-soluble synthetic polymer at a position other than the N-terminus, and wherein the amino acid sequence of the first neublastin polypeptide and the second neublastin polypeptide are the same and are selected from the group consisting of NBN113 (SEQ ID NO:2), NBN140 (SEQ ID NO:6), NBN116 (SEQ ID NO:7), NBN112 (SEQ ID NO:8), NBN111 (SEQ ID NO:9), NBN110 (SEQ ID NO:10), NBN109 (SEQ ID NO:11), NBN108 (SEQ ID NO:12), NBN107 (SEQ ID NO:13), NBN106 (SEQ ID NO:14), NBN105 (SEQ ID NO:15), NBN104 (SEQ ID NO:16), NBN103 (SEQ ID NO:17), NBN102 (SEQ ID NO:18), NBN101 (SEQ ID NO:19), NBN100 (SEQ ID NO:20) and NBN99 (SEQ ID NO:21).

2. The dimer of claim 1 , wherein the water-soluble synthetic polymer is a polyalkylene glycol moiety.

3. The dimer of claim 1 , wherein the N-terminal amino acid of the first neublastin polypeptide and the N-terminal amino acid of the second neublastin polypeptide each is conjugated to a polyalkylene glycol moiety.

4. The dimer of claim 2 , wherein the polyalkylene glycol moiety is a polyethylene glycol moiety.

5. The dimer of claim 4 , wherein at least one of the polypeptides is glycosylated at the asparagine residue corresponding to the asparagine at position 95 of SEQ ID NO:2.

6. The dimer of claim 1 , wherein the N-terminal amino acid of the first neublastin polypeptide and the N-terminal amino acid of the second neublastin polypeptide each is conjugated to a polyethylene glycol moiety.

7. The dimer of claim 6 , wherein at least one of the polypeptides is glycosylated at the asparagine residue corresponding to the asparagine at position 95 of SEQ ID NO:2.

8. A composition comprising the dimer of claim 1 and a pharmaceutically acceptable carrier.

9. A method of treating neuropathic pain in a human in need thereof, comprising administering to the human a therapeutically effective amount of the dimer of claim 1 .

10. A method of treating a peripheral neuropathy in a human in need thereof, comprising administering to the human a therapeutically effective amount of the dimer of claim 1 .

11. A method of treating painful diabetic neuropathy in a human in need thereof, comprising administering to the human a therapeutically effective amount of the dimer of claim 1 .

12. A dimer comprising a first neublastin polypeptide and a second neublastin polypeptide, wherein: (a) at least one of the polypeptides is glycosylated; (b) at least one of the polypeptides is conjugated at its N-terminus to a polyalkylene glycol moiety; and (c) neither of the polypeptides is conjugated to a polyalkylene glycol moiety at a position other than the N-terminus, and wherein the amino acid sequence of the first neublastin polypeptide and the second neublastin polypeptide is NBN104 (SEQ ID NO:16).

13. The dimer of claim 12 , wherein the N-terminal amino acid of the first neublastin polypeptide and the N-terminal amino acid of the second neublastin polypeptide each is conjugated to a polyalkylene glycol moiety.

14. A composition comprising the dimer of claim 12 and a pharmaceutically acceptable carrier.

15. A method of treating neuropathic pain in a human in need thereof, comprising administering to the human a therapeutically effective amount of the dimer of claim 12 .

16. A method of treating a peripheral neuropathy in a human in need thereof, comprising administering to the human a therapeutically effective amount of the dimer of claim 12 .

17. A method of treating painful diabetic neuropathy in a human in need thereof, comprising administering to the human a therapeutically effective amount of the dimer of claim 12 .

18. A homodimer comprising a first neublastin polypeptide and a second neublastin polypeptide, wherein the amino acid sequence of the first neublastin polypeptide and the second neublastin polypeptide is NBN104 (SEQ ID NO:16), wherein each of the neublastin polypeptides is conjugated to a polyethylene glycol moiety at its amino terminus and is glycosylated at the asparagine residue corresponding to the asparagine at position 95 of SEQ ID NO:2, and wherein neither of the polypeptides is conjugated to a polyethylene glycol moiety at a position other than the N-terminus.

19. A composition comprising the homodimer of claim 18 and a pharmaceutically acceptable carrier.

20. A method of treating neuropathic pain in a human in need thereof, comprising administering to the human a therapeutically effective amount of the homodimer of claim 18 .

21. A method of treating a peripheral neuropathy in a human in need thereof, comprising administering to the human a therapeutically effective amount of the homodimer of claim 18 .

22. A method of treating painful diabetic neuropathy in a human in need thereof, comprising administering to the human a therapeutically effective amount of the homodimer of claim 18 .

Assignments (5)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 3, 2022
From: GLORIANA THERAPEUTICS, INC.
To: SINFONIA BIOTHERAPEUTICS AB
Reel/Frame 060711/0374 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 26, 2019
From: GLORIANA THERAPEUTICS SARL
To: GLORIANA THERAPEUTICS, INC.
Reel/Frame 049005/0877 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 6, 2017
From: BIOGEN MA INC.
To: GLORIANA THERAPEUTICS SARL
Reel/Frame 041887/0117 →
CHANGE OF NAME Recorded May 4, 2015
From: BIOGEN IDEC MA INC.
To: BIOGEN MA INC.
Reel/Frame 035571/0926 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 17, 2013
From: SAH, DINAH WEN-YEE; PEPINSKY, R. BLAKE; ROSSOMANDO, ANTHONY
To: BIOGEN IDEC MA INC.
Reel/Frame 030624/0899 →