IP Library Granted Patent US 10,119,979
Granted Patent B2
US 10,119,979 · App. 12/301,988 · Granted Nov 6, 2018

Methods of treating stroke and traumatic brain injury using humanized AQC2 anti-VLA-1 antibodies

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Quick Facts
Patent No.
US 10,119,979
App. No.
12/301,988
Granted
Nov 6, 2018
Kind
B2
Abstract

Methods and compositions for treating stroke are disclosed.

Claims (19)

1. A method of treating a traumatic brain injury (TBI) in a subject, the method comprising administering to the subject a humanized AQC2 anti-VLA-1 (Very Late Activation Antigen-I) antibody, or an antigen-binding fragment thereof, wherein the anti-VLA-1 antibody, or antigen-binding fragment thereof, is first administered within 48 hours of the TBI, and wherein the anti-VLA-1 antibody, or antigen-binding fragment thereof, reduces infarct size in a hemisphere affected by the TBI, such that the percentage of the hemisphere infarcted is 40% or less, and wherein the anti-VLA-1 antibody or antigen-binding fragment thereof is administered at a dosage from 0.1 mg/kg per day to 5 mg/kg per day.

2. The method of claim 1 , wherein the TBI is a contusion, bruise, laceration or hematoma.

3. The method of claim 1 , wherein the administering step reduces the infarct size by at least 10% in the hemisphere affected by the TBI, as compared to an infarct size in an untreated subject.

4. The method of claim 1 , wherein the administering step reduces the infarct size by at least 20% in the hemisphere affected by the TBI, as compared to an infarct size in an untreated subject.

5. The method of claim 1 , wherein the administering step reduces edema, such that the size of the hemisphere affected by the TBI is increased by no more than 10% following the TBI.

6. A method of treating a stroke in a subject, the method comprising administering to the subject a humanized AQC2 anti-VLA-1 (Very Late Activation Antigen-1) antibody, or an antigen-binding fragment thereof, wherein the anti-VLA-1 antibody, or antigen-binding fragment thereof, is first administered within 48 hours of the stroke, and wherein the anti-VLA-1 antibody, or antigen-binding fragment thereof, reduces infarct size in a hemisphere affected by the stroke, such that the percentage of the hemisphere infarcted is 40% or less, and wherein the anti-VLA-1 antibody or antigen-binding fragment thereof is administered at a dosage from 0.1 mg/kg per day to 5 mg/kg per day.

7. The method of claim 6 , wherein the humanized AQC2 anti-VLA-1 antibody, or antigen-binding fragment thereof, is produced by a hybridoma having ATCC Deposit No. PTA3275.

8. The method of claim 6 , wherein the anti-VLA-1 antibody or antigen-binding fragment thereof is effective to improve neurologic function.

9. The method of claim 6 , wherein the stroke is an ischemic stroke.

10. The method of claim 6 , wherein the stroke is an hemorrhagic stroke.

11. The method of claim 6 , wherein the subject is a mammal.

12. The method of claim 11 , wherein the subject is a human.

13. The method of claim 6 , wherein the anti-VLA-1 antibody or antigen-binding fragment thereof is administered intravenously or parenterally.

14. The method of claim 6 , wherein the anti-VLA-1 antibody or antigen-binding fragment thereof is administered at least twice within 7 days after the stroke.

15. The method of claim 6 , wherein the administering step reduces the infarct size by at least 10% in the hemisphere affected by the stroke, as compared to an infarct size in an untreated subject.

16. The method of claim 6 , wherein the administering step reduces the infarct size by at least 20% in the hemisphere affected by the stroke, as compared to an infarct size in an untreated subject.

17. The method of claim 6 , wherein the administering step reduces edema, such that the size of the hemisphere affected by the stroke is increased by no more than 10% following the stroke.

18. The method of claim 6 , wherein the anti-VLA-1 antibody or antigen-binding fragment thereof is administered in combination with another therapeutic agent.

19. The method of claim 18 , wherein the other therapeutic agent is selected from the group consisting of an antiplatelet agent, a thrombolytic enzyme, an aggregation inhibitor, a glycoprotein IIb/IIIa inhibitor, a glycosaminoglycan, a thrombin inhibitor, an anticoagulant, heparin, coumarin, tPA, GCSF, streptokinase, urokinase, Ancrod, acetylsalicyclic acid, melatonin, and a caspase inhibitor.

Assignments (3)
CHANGE OF NAME Recorded May 4, 2015
From: BIOGEN IDEC MA INC.
To: BIOGEN MA INC.
Reel/Frame 035571/0926 →
CHANGE OF NAME Recorded Apr 29, 2015
From: BIOGEN IDEC MA INC.
To: BIOGEN MA INC.
Reel/Frame 035532/0566 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 20, 2009
From: RELTON, JANE K.; GARDNER, HUMPHREY
To: BIOGEN IDEC MA INC.
Reel/Frame 023548/0101 →