IP Library Granted Patent US 7,655,230
Granted Patent B2
US 7,655,230 · App. 12/107,050 · Granted Feb 2, 2010

Co-administration of a tissue plasminogen activator, anti-CD11b antibody and anti-CD18 antibody in stroke

Assignee: Genentech, Inc.
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Quick Facts
Patent No.
US 7,655,230
App. No.
12/107,050
Granted
Feb 2, 2010
Kind
B2
Abstract

A method for improving clinical outcome in focal ischemic stroke in a mammal by increasing cerebral blood flow and/or reducing infarct size is described which involves administering an effective amount of an anti-CD18 antibody to the mammal, in the absence of removal of the arterial obstruction.

Claims (18)

1. A method for increasing cerebral blood flow and/or reducing infarct size in focal ischemic stroke caused by obstruction of a main cerebral artery in a human mammal which comprises the step of co-administering effective amounts of tissue plasminogen activator (tPA), anti-CD11b antibody, and anti-CD18 antibody to the mammal wherein neither the tPA nor the anti-CD18 antibody is administered to the mammal until about three to five hours after the onset of focal ischemic stroke.

2. The method of claim 1 that increases cerebral blood flow and reduces infarct size in the mammal.

3. The method of claim 1 wherein the anti-CD11b antibody is an antibody fragment.

4. The method of claim 3 wherein the anti-CD11b antibody fragment is a F(ab′) 2 .

5. The method of claim 1 wherein the anti-CD11b antibody is humanized.

6. The method of claim 1 wherein the anti-CD11b antibody is administered to the mammal by bolus dosage.

7. The method of claim 1 wherein the anti-CD11b antibody is administered intravenously.

8. The method of claim 1 wherein the anti-CD11b antibody is administered via continuous infusion.

9. The method of claim 1 wherein the anti-CD11b antibody and the tPA are simultaneously administered to the mammal.

10. The method of claim 1 wherein the anti-CD11b antibody is administered before the tPA is administered to the mammal.

11. The method of claim 1 wherein the anti-CD11b antibody is a humanized anti-CD11b antibody.

12. The method of claim 11 wherein the humanized anti-CD11b antibody is a F(ab′) 2 .

13. The method of claim 1 , wherein the anti-CD18 antibody binds to an extracellular domain of CD18 and inhibits or reduces the ability of a cell expressing CD18 to bind to endothelium.

14. The method of claim 1 , wherein the anti-CD18 antibody binds CD18 with an affinity of 4 nM or less.

15. The method of claim 1 , wherein the anti-CD18 antibody binds CD18 with an affinity of 3 nM or less.

16. The method of claim 1 , wherein the anti-CD18 antibody binds CD18 with an affinity of 1 nM or less.

17. The method of claim 1 , wherein the anti-CD18 antibody dissociates the CD11b/CD18 complex.

18. The method of claim 1 , wherein the anti-CD18 antibody is a humanized H52 antibody comprising a heavy chain sequence of SEQ ID NO:10 or SEQ ID NO: 12 and comprising a light chain sequence of SEQ ID NO: 11.

Assignments (1)
CONFIRMATORY LICENSE Recorded Jun 16, 2025
From: UNIVERSITY OF VERMONT & ST AGRIC COLLEGE
To: NATIONAL INSTITUTES OF HEALTH
Reel/Frame 071645/0027 →
Continuity (7)
Continuation 1102571200 · Dec 28, 2004
Continuation 1040428600 · Mar 31, 2003
Continuation 0981138400 · Dec 20, 2000
Continuation 0925165200 · Feb 17, 1999
Continuation In Part 0878880000 · Jan 22, 1997
Provisional Application 6009303800 · Jan 23, 1996
Related Publication 20090274689A1 · Nov 5, 2009