IP Library Granted Patent US 7,357,925
Granted Patent B2
US 7,357,925 · App. 10/649,609 · Granted Apr 15, 2008

Method for treating disorders and diseases treatable with human fibroblast interferon

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Quick Facts
Patent No.
US 7,357,925
App. No.
10/649,609
Granted
Apr 15, 2008
Kind
B2
Abstract

PEG-IFN-β conjugates, where a PEG moiety is covalently bound to Cys 17 of human IFN-β, are produced by a process of site specific PEGylation with a thiol reactive PEGylating agent. A pharmaceutical composition and a method for treating infections, tumors and autoimmune and inflammatory diseases are also provided. The invention further relates to a method for the stepwise attachment of PEG moieties in series to a polypeptide, and more particularly to IFN-β.

Claims (19)

1. A method for treating viral infections, lupus erythematosus, or rheumatoid arthritis or for stimulating natural killer cells against neoplastic cells, comprising administering an effective amount of a polyol-human fibroblast interferon (interferon-β) conjugate having a polyol moiety covalently bound to Cys 17 of human fibroblast interferon to a subject in need thereof.

2. The method according to claim 1 , wherein the polyol-human fibroblast interferon conjugate has the same or higher antiviral and antiproliferative activity as human fibroblast interferon.

3. The method of claim 1 , which treats viral infections.

4. The method of claim 1 , which treats lupus erythematosus.

5. The method of claim 1 , which treats rheumatoid arthritis.

6. The method of claim 1 , which stimulates natural killer cells against neoplastic cells.

7. The method according to claim 1 , wherein said polyol moiety is a polyalkylene glycol moiety.

8. The method according to claim 7 , wherein said polyalkylene glycol moiety is a polyethylene glycol (PEG) moiety.

9. A method for treating multiple sclerosis, comprising administering an effective amount of a polyol-human fibroblast interferon (interferon-β) conjugate having a polyol moiety covalently bound to Cys 17 of human fibroblast interferon to a subject in need thereof.

10. The method of claim 9 , wherein said polyol moiety is a polyalkylene glycol moiety.

11. The method of claim 10 , wherein said polyalkylene glycol moiety is a polyethylene glcol (PEG) moiety.

12. An improved method for treating multiple sclerosis, viral infections, rheumatoid arthritis, or lupus erythematosus, or for stimulating natural killer cells against neoplastic cells, which comprises administering an effective amount of human fibroblast interferon (interferon-β) to a subject in need thereof, wherein the improvement comprises human fibroblast interferon which is a polyol-human fibroblast interferon conjugate having a polyol moiety covalently bound to Cys 17 of human fibroblast interferon.

13. The method of claim 12 , which treats multiple sclerosis.

14. The method of claim 12 , which treats viral infections.

15. The method of claim 12 , which treats lupus erythematosus.

16. The method of claim 12 , which treats rheumatoid arthritis.

17. The method of claim 12 , which stimulates natural killer cells against neoplastic cells.

18. The method of claim 12 , wherein said polyol moiety is a polyalkylene glycol moiety.

19. The method of claim 18 , wherein said polyalkylene glycol moiety is a polyethylene glycol (PEG) moiety.

Assignments (2)
CHANGE OF NAME Recorded Nov 25, 2009
From: LABORATOIRES SERONO SA
To: MERCK SERONO SA
Reel/Frame 023569/0120 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 11, 2007
From: APPLIED RESEARCH SYSTEMS ARS HOLDING N.V.
To: LABORATOIRES SERONO SA
Reel/Frame 019966/0026 →