IP Library Granted Patent US 6,989,365
Granted Patent B2
US 6,989,365 · App. 10/702,536 · Granted Jan 24, 2006

Methods of treatment with erythropoietin and albumin fusion protein

Assignee: Aventis Behring L.L.C.
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Quick Facts
Patent No.
US 6,989,365
App. No.
10/702,536
Granted
Jan 24, 2006
Kind
B2
Abstract

Biologically active polypeptides comprising a therapeutically active polypeptide fused to human serum albumin or a variant thereof, methods for the preparation thereof, nucleotide sequences encoding such fusion polypeptides, expression cassettes comprising such nucleotide sequences, self-replicating plasmids containing such expression cassettes, and pharmaceutical compositions containing said fusion polypeptides.

Claims (29)

1. method of treating a patient in need of erythropoietin, comprising the step of administering a fusion protein comprising erythropoietin and albumin or an albumin variant, wherein (i) said fusion protein has a higher plasma stability than unfused erythropoietin, (ii) said fusion protein retains the therapeutic activity of unfused erythropoietin, and (iii) said albumin or albumin variant is located either at the N-terminus or C-terminus of said fusion protein.

2. The method of claim 1 , wherein said fusion protein comprises albumin.

3. The method of claim 1 , wherein said fusion protein comprises an albumin variant.

4. The method of claim 3 , wherein said albumin variant is a fragment of albumin.

5. The method of claim 3 , wherein said albumin variant has a mutation of one or more residues.

6. The method of claim 3 , wherein said albumin variant has a deletion of one or more residues.

7. The method of claim 3 , wherein said albumin variant has a mutation and a deletion of one or more residues.

8. The method of claim 3 , wherein said albumin variant has an addition of one or more residues.

9. The method of claim 1 , wherein said fusion protein comprises an N-terminal methionine.

10. The method of claim 1 , wherein said fusion protein comprises a peptide linker.

11. The method of claim 1 , wherein said fusion protein comprises a secretion signal sequence.

12. The method of claim 11 , wherein said secretion signal sequence is the natural leader sequence of erythropoietin.

13. The method of claim 1 , wherein said erythropoietin is fused to the N-terminal end of said albumin or albumin variant.

14. The method of claim 1 , wherein said erythropoietin is fused to the C-terminal end of said albumin or albumin variant.

15. A method of treating a patient in need of erthyropoietin, comprising the step of administering a fusion protein comprising erythropoietin and a mature form of albumin, wherein (i) said fusion protein has a higher plasma stability than unfused erythropoietin, (ii) said fusion protein retains the therapeutic activity of unfused erythropoietin, and (iii) said albumin or albumin variant is located either at the N-terminus or C-terminus of said fusion protein.

16. The method of claim 15 , wherein said fusion protein comprises an N-terminal methionine.

17. The method of claim 15 , wherein said fusion protein comprises a peptide linker.

18. The method of claim 15 , wherein said fusion protein comprises a secretion signal sequence.

19. The method of claim 18 , wherein said secretion signal sequence is the natural leader sequence of erythropoietin.

20. The method of claim 15 , wherein said erythropoietin is fused to the N-terminal end of said mature form of albumin.

21. The method of claim 20 , wherein said fusion protein comprises an N-terminal methionine.

22. The method of claim 20 , wherein said fusion protein comprises a peptide linker.

23. The method of claim 20 , wherein said fusion protein comprises a secretion signal sequence.

24. The method of claim 23 , wherein said secretion signal sequence is the natural leader sequence of erythropoietin.

25. The method of claim 15 , wherein said erythropoietin is fused to the C-terminal end of said mature form of albumin.

26. The method of claim 25 , wherein said fusion protein comprises an N-terminal methionine.

27. The method of claim 25 , wherein said fusion protein comprises a peptide linker.

28. The method of claim 25 , wherein said fusion protein comprises a secretion signal sequence.

29. A The method of claim 28 , wherein said secretion signal sequence is the natural leader sequence of erythropoietin.

Assignments (4)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 7, 2010
From: NOVOZYMES BIOPHARMA UK LIMITED
To: NOVOZYMES BIOPHARMA DK A/S
Reel/Frame 025105/0517 →
CHANGE OF NAME Recorded Dec 31, 2007
From: NOVOZYMES DELTA LIMITED
To: NOVOZYMES BIOPHARMA UK LIMITED
Reel/Frame 020299/0491 →
CHANGE OF NAME Recorded Dec 31, 2007
From: DELTA BIOTECHNOLOGY LIMITED
To: NOVOZYMES DELTA LIMITED
Reel/Frame 020299/0814 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 11, 2006
From: AVENTIS BEHRING L.L.C.
To: DELTA BIOTECHNOLOGY LTD.
Reel/Frame 017921/0492 →
Priority Claims (1)
FR 92 01064 · Jan 31, 1992 · national
Continuity (5)
Division 0998418600 · Oct 29, 2001
Continuation 0925853200 · Feb 26, 1999
Division 0879768900 · Jan 31, 1997
Continuation 0825692700
Related Publication 20040086976A1 · May 6, 2004