IP Library Granted Patent US 7,348,004
Granted Patent B2
US 7,348,004 · App. 11/029,003 · Granted Mar 25, 2008

Immunoglobulin chimeric monomer-dimer hybrids

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Quick Facts
Patent No.
US 7,348,004
App. No.
11/029,003
Granted
Mar 25, 2008
Kind
B2
Abstract

The invention relates to a chimeric monomer-dimer hybrid protein wherein said protein comprises a first and a second polypeptide chain, said first polypeptide chain comprising at least a portion of an immunoglobulin constant region and a biologically active molecule, and said second polypeptide chain comprising at least a portion of an immunoglobulin constant region without the biologically active molecule of the first chain. The invention also relates to methods of using and methods of making the chimeric monomer-dimer hybrid protein of the invention.

Claims (44)

1. A method of treating a subject with a disease or condition comprising administering a pharmaceutically effective amount of a monomer-dimer hybrid immunoconjugate to the subject, wherein the immunoconjugate comprises

X-L a -F 1 :F 2 or F 2 :F 1 -L a -X,

wherein:

X is a single biologically active molecule capable of treating the disease or condition;

L is a linker;

a is any integer or zero;

: represents a chemical association;

F 1 is at least a portion of an immunoglobulin constant region comprising an FcRn binding site and does not comprise a biologically active molecule,

F 2 is at least a portion of an immunoglobulin constant region comprising an FcRn binding site; and does not comprise a biologically active molecule or immunoglobulin variable region.

2. The method of claim 1 , wherein said monomer-dimer hybrid immunoconjugate is administered intravenously, subcutaneously, orally, buccally, sublingually, nasally, parenterally, rectally, vaginally or via a pulmonary route.

3. The method of claim 1 , wherein said disease or condition is a viral infection.

4. The method of claim 1 , wherein X is interferon.

5. The method of claim 4 , wherein the interferon is interferon α and L consists of 15-25 amino acids.

6. The method of claim 5 , wherein L consists of 15-20 amino acids.

7. The method of claim 1 , wherein said disease or condition is a hemostatic disorder.

8. The method of claim 1 , wherein said disease or condition is hemophilia A.

9. The method of claim 1 , wherein said disease or condition is hemophilia B.

10. The method of claim 1 , wherein X is Factor VII or Factor VIIa.

11. The method of claim 1 , wherein X is Factor IX.

12. The method of claim 1 , wherein said disease or condition is anemia.

13. The method of claim 1 , wherein X is erythropoietin.

14. The method of claim 4 , wherein the interferon is interferon α.

15. The method of claim 4 , wherein the interferon is interferon β.

16. The method of claim 1 , wherein the disease or condition is a cardiovascular disease or condition.

17. The method of claim 16 , wherein the cardiovascular disease or condition is chosen from stroke, brain ischemia, cerebral ischemia, myocardial ischemia, cardiac ischemia, isehemic heart disease, myocardial infarction, coronary artery disease, acute coronary syndrome, artheroselerosis, chronic heart failure, congestive heart failure, and reperfusion injury.

18. The method of claim 16 , wherein X is erythropoietin.

19. A method of treating a subject with a disease or condition comprising administering a pharmaceutically effective amount of a monomer-dimer hybrid immunoconjugate to the subject, wherein the immunoconjugate consists of the formula

X-L a -F 1 :F 2 -T or T-F 2 :F 1 -L a -X,

wherein:

X is a single biologically active molecule capable of treating the disease or condition;

L is a linker, a is any integer or zero;

T is a molecule having a molecular weight less than 2 kD;

: represents a chemical association;

F 1 is at least a portion of an immunoglobulin constant region comprising an FcRn binding site; and

F 2 is at least a portion of an immunoglobulin constant region comprising an FcRn binding site.

20. A method of providing improved delivery of a biologically active molecule comprising administering to a subject a monomer-dimer hybrid immunoconjugate comprising

X-L a -F 1 :F 2 or F 2 :F 1 -L a -X,

wherein:

X is a single biologically active molecule capable of treating the disease or condition;

L is a linker;

a is any integer or zero;

: represents a chemical association;

F 1 is at least a portion of an immunoglobulin constant region comprising an FcRn binding site and does not comprise a biologically active molecule; and

F 2 is at least a portion of an immunoglobulin constant region comprising an FcRn binding site and does not comprise a biologically active molecule or immunoglobulin variable region.

Assignments (7)
CHANGE OF NAME Recorded Feb 16, 2017
From: BIOGEN HEMOPHILIA INC.
To: BIOVERATIV THERAPEUTICS INC.
Reel/Frame 041735/0621 →
CHANGE OF ADDRESS Recorded Jul 2, 2015
From: BIOGEN HEMOPHILIA INC.
To: BIOGEN HEMOPHILIA INC.
Reel/Frame 036051/0773 →
CHANGE OF NAME Recorded Apr 30, 2015
From: BIOGEN IDEC HEMOPHILIA INC.
To: BIOGEN HEMOPHILIA INC.
Reel/Frame 035553/0325 →
CHANGE OF NAME Recorded Apr 24, 2014
From: SYNTONIX PHARMACEUTICALS, INC.
To: BIOGEN IDEC HEMOPHILIA INC.
Reel/Frame 032753/0837 →
RELEASE & REASSIGNMENT Recorded Mar 5, 2007
From: BIOGEN IDEC INC.
To: SYNTONIX PHARMACEUTICALS, INC.
Reel/Frame 018964/0431 →
SECURITY AGREEMENT Recorded Jan 12, 2007
From: SYNTONIX PHARMACEUTICALS, INC.
To: BIOGEN IDEC INC.
Reel/Frame 018764/0586 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 3, 2006
From: PETERS, ROBERT T.; MEZO, ADAM R.; RIVERA, DANIEL S.; BITONI, ALAN J.; STATTEL, JAMES; LOW, SUSAN C.
To: SYNTONIX PHARMACEUTICALS, INC.
Reel/Frame 017160/0064 →