US2002081294A1PendingUtilityA1

Co-administration of a thrombolytic and an anti-CD18 antibody in stroke

Assignee: GENENTECH INCPriority: Jan 23, 1996Filed: Dec 20, 2000Published: Jun 27, 2002
Est. expiryJan 23, 2016(expired)· nominal 20-yr term from priority
A61K 39/3955C07K 16/2845C07K 2317/24A61P 9/00C07K 16/2821C07K 2317/76A61K 38/49C07K 2317/54A61K 2039/505
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Claims

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 ant-CD18 antibody to the mammal, in the absence of removal of the arterial obstruction.

Claims

exact text as granted — not AI-modified
1 . A method for increasing cebral blood flow and/or reducing interfact size in focal ischemic stroke caused by obstruction of a main cerebral artery in a human mammal which comprise the step of co-administering effective amounts of tissue plasminogen actiator (tPA) and ati-CD18 antibody to 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 ischmic stroke.  
     
     
         2 . The method of  claim 1  that increase cerebral blood flow and reduces infarct cizo in the mammal.  
     
     
         3 . The method of  claim 1  wherein the anti-CD18 antibody is an antibody fragment.  
     
     
         4 . The method of  claim 3  wherein the anti-CD18 antibody fragment is a F(ab) 2 .  
     
     
         5 . The method of  claim 1  wherein the anti-CD18 antibody is humanized.  
     
     
         6 . The method of  claim 1  wherein the anti-CD18 antibody is administered to the mammal by bolus dosage.  
     
     
         7 . The method of  claim 1  wherein the anti-CD18 antibody is administered inravenously.  
     
     
         8 . The method of  claim 1  wherein the anti-CD18 antibody is administered via cotinuos infusion.  
     
     
         9 . The method of  claim 1  wherein the anti-CD18 antibody and the tPA are simulteneously administered to the mammal.  
     
     
         10 . The method of  claim 1  wherein the anti-CD18 antibody is administered before the tPA is administered to the mammal.  
     
     
         11 . The method of  claim 1  wherein the anti-CD18 antibody is humanized H52 antibody comprising heavy chain sequence of SEQ ID NO: 10 and light chain sequence of SEQ ID NO: 11.  
     
     
         12 . The method of  claim 1  wherein the H52 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 binds to the epitope bound by H52 antibody.

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