IP Library Granted Patent US 8,557,240
Granted Patent B2
US 8,557,240 · App. 13/296,778 · Granted Oct 15, 2013

Method for the treatment of inflammatory disorders

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Quick Facts
Patent No.
US 8,557,240
App. No.
13/296,778
Granted
Oct 15, 2013
Kind
B2
Abstract

A method for the treatment of inflammatory disorders is disclosed, particularly the treatment of arthritis. The method comprises the administration of a function blocking antibody which is capable of binding an epitope of VLA-1.

Claims (20)

1. A monoclonal antibody or antigen binding fragment thereof, wherein the antibody or antigen binding fragment thereof is capable of specifically binding an epitope of VLA-1, wherein the epitope comprises amino acid residues Val-Gln-Arg-Gly-Gly-Arg (SEQ ID NO:8) and wherein the antibody or fragment of said antibody is capable of binding a human α1-I domain but not to a rat α1-I domain, and wherein said epitope is cation-dependent.

2. The antibody or antigen binding fragment of claim 1 , wherein the antibody or antigen binding fragment is capable of decreasing arthritic score about 79% or greater.

3. The antibody or antigen binding fragment of claim 1 , wherein the antibody or antigen binding fragment is capable of decreasing arthritic score about 85% or greater.

4. The antibody or antigen binding fragment of claim 1 , wherein the antibody or antigen binding fragment is capable of decreasing arthritic score about 90% or greater.

5. The antibody or antigen binding fragment of claim 1 , wherein the antibody is produced by a hybridoma designated by American Type Culture Collection (ATCC) Deposit Number PTA-3580.

6. The antibody or antigen binding fragment of claim 1 , wherein the antibody or antigen binding fragment is capable of decreasing arthritic score about 65% or greater.

7. A pharmaceutical composition comprising the antibody or antigen binding fragment of claim 1 and a pharmaceutically acceptable carrier.

8. The pharmaceutical composition of claim 7 , wherein the composition is suitable for administration parenterally.

9. The pharmaceutical composition of claim 7 , wherein the composition is suitable for administration orally, subcutaneously, intravenously, intramuscularly, intraarticularly, intra-synovially, intrasternally, intrathecally, intrahepatically, intralesionally, intracranially, intraparenterally or intranasally.

10. The pharmaceutical composition of claim 7 , wherein the composition is suitable for administration to a subject in an amount between about 0.1 mg/kg/day to about 50 mg/kg/day.

11. The pharmaceutical composition of claim 7 , wherein the composition is suitable for administration to a subject in an amount between about 0.1 mg/kg/day to about 20 mg/kg/day.

12. The pharmaceutical composition of claim 7 , wherein the composition is suitable for administration to a subject in an amount between about 0.1 mg/kg/day to about 10 mg/kg/day.

13. The pharmaceutical composition of claim 7 , wherein the composition is suitable for administration to a subject in an amount between about 0.3 mg/kg/day to about 1 mg/kg/day.

14. The pharmaceutical composition of claim 7 , wherein the composition is suitable for administration to a subject in an amount between about 5 mg/kg/day to about 12.5 mg/kg/day.

15. The pharmaceutical composition of claim 7 , wherein the composition is suitable for administration to a subject in an amount at intervals of every one to 14 days.

16. The pharmaceutical composition of claim 7 , for treating arthritis.

17. The pharmaceutical composition of claim 7 , for blocking an interaction between VLA-1 and collagen.

18. The pharmaceutical composition of claim 7 , for blocking an interaction between VLA-1 and collagen IV.

19. The antibody or antigen binding fragment of claim 1 , wherein the antibody or fragment thereof inhibits binding of K562-α1 cells to collagen IV coated plates, and wherein the inhibitory activity plateaus at about 0.6 μg/mL antibody.

20. The pharmaceutical composition of claim 7 , wherein the antibody or fragment thereof inhibits binding of K562-α1 cells to collagen IV coated plates, and wherein the inhibitory activity plateaus at about 0.6 μg/mL antibody.

Assignments (4)
CHANGE OF NAME Recorded May 4, 2015
From: BIOGEN IDEC MA INC.
To: BIOGEN MA INC.
Reel/Frame 035571/0926 →
CHANGE OF NAME Recorded May 1, 2015
From: BIOGEN IDEC MA INC.
To: BIOGEN MA INC.
Reel/Frame 035552/0952 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 17, 2011
From: GOTWALS, PHILIP; DE FOUGEROLLES, ANTONIN; LOBB, ROY; KOTELIANSKI, VICTOR
To: BIOGEN, INC.
Reel/Frame 027246/0107 →
CHANGE OF NAME Recorded Nov 17, 2011
From: BIOGEN, INC.
To: BIOGEN IDEC MA INC.
Reel/Frame 027248/0401 →