IP Library Granted Patent US 8,217,146
Granted Patent B2
US 8,217,146 · App. 12/632,517 · Granted Jul 10, 2012

Neurotrophic factors and methods of use thereof

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Quick Facts
Patent No.
US 8,217,146
App. No.
12/632,517
Granted
Jul 10, 2012
Kind
B2
Abstract

The invention relates to neublastin neurotrophic factor polypeptides, nucleic acids encoding neublastin polypeptides, and antibodies that bind specifically to neublastin polypeptides, as well as methods of making and methods of using the same.

Claims (33)

1. An isolated polypeptide that possesses neurotrophic activity and is at least 95% identical to amino acids 37-140 of SEQ ID NO:9, wherein the polypeptide consists of 104 amino acids.

2. The polypeptide of claim 1 , wherein the polypeptide is at least 98% identical to amino acids 37-140 of SEQ ID NO:9.

3. The polypeptide of claim 1 , wherein the polypeptide is at least 99% identical to amino acids 37-140 of SEQ ID NO:9.

4. The polypeptide of claim 1 , wherein the polypeptide is glycosylated.

5. The polypeptide of claim 2 , wherein the polypeptide is glycosylated.

6. The polypeptide of claim 3 , wherein the polypeptide is glycosylated.

7. A pharmaceutical composition comprising the polypeptide of claim 1 and a pharmaceutically acceptable carrier.

8. A pharmaceutical composition comprising the polypeptide of claim 2 and a pharmaceutically acceptable carrier.

9. A pharmaceutical composition comprising the polypeptide of claim 3 and a pharmaceutically acceptable carrier.

10. A pharmaceutical composition comprising the polypeptide of claim 4 and a pharmaceutically acceptable carrier.

11. A pharmaceutical composition comprising the polypeptide of claim 5 and a pharmaceutically acceptable carrier.

12. A pharmaceutical composition comprising the polypeptide of claim 6 and a pharmaceutically acceptable carrier.

13. A method of treating neuropathic pain in a mammal, comprising administering to the mammal a therapeutically effective amount of a pharmaceutical composition comprising (a) the polypeptide of claim 1 , and (b) a pharmaceutically acceptable carrier.

14. A method of treating a peripheral neuropathy in a mammal, comprising administering to the mammal a therapeutically effective amount of a pharmaceutical composition comprising (a) the polypeptide of claim 1 , and (b) a pharmaceutically acceptable carrier.

15. The method of claim 14 , wherein the peripheral neuropathy is diabetic peripheral neuropathy.

16. The method of claim 13 , wherein the pharmaceutical composition is administered systemically.

17. The method of claim 13 , wherein the mammal is a human.

18. The method of claim 14 , wherein the pharmaceutical composition is administered systemically.

19. The method of claim 14 , wherein the mammal is a human.

20. The method of claim 15 , wherein the pharmaceutical composition is administered systemically.

21. The method of claim 15 , wherein the mammal is a human.

22. A method of treating neuropathic pain in a mammal, comprising administering to the mammal a therapeutically effective amount of a pharmaceutical composition comprising (a) the polypeptide of claim 2 , and (b) a pharmaceutically acceptable carrier.

23. A method of treating a peripheral neuropathy in a mammal, comprising administering to the mammal a therapeutically effective amount of a pharmaceutical composition comprising (a) the polypeptide of claim 2 , and (b) a pharmaceutically acceptable carrier.

24. The method of claim 23 , wherein the peripheral neuropathy is diabetic peripheral neuropathy.

25. The method of claim 22 , wherein the pharmaceutical composition is administered systemically.

26. The method of claim 22 , wherein the mammal is a human.

27. The method of claim 23 , wherein the pharmaceutical composition is administered systemically.

28. The method of claim 23 , wherein the mammal is a human.

29. The method of claim 24 , wherein the pharmaceutical composition is administered systemically.

30. The method of claim 24 , wherein the mammal is a human.

31. A method of activating a Rearranged During Transfection (RET) receptor tyrosine kinase, the method comprising contacting a cell expressing RET and Glial Cell Line-Derived Neurotrophic Factor Family Receptor Alpha-3 (GFRalpha3) with an amount of a dimerized protein effective to bind to a complex comprising RET and GFRalpha3 and induce dimerization and autophosphorylation of RET, thereby activating the RET receptor tyrosine kinase, wherein the dimerized protein possesses neurotrophic activity and is a homodimer consisting of two polypeptides each of which consists of an amino acid sequence that is 104 amino acids in length and is at least 95% identical to amino acids 37-140 of SEQ ID NO:9.

32. The method of claim 31 , wherein the cell is a nerve or neuronal cell.

33. The method of claim 31 , wherein the cell is a human cell.

Assignments (6)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 5, 2023
From: GLORIANA THERAPEUTICS
To: SINFONIA BIOTHERAPEUTICS AB
Reel/Frame 062287/0670 →
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 Jan 14, 2010
From: SAH, DINAH W.Y.; ROSSOMANDO, ANTHONY
To: BIOGEN IDEC MA INC.
Reel/Frame 023784/0518 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 14, 2010
From: JOHANSEN, TEIT E.
To: NSGENE A/S
Reel/Frame 023784/0590 →