US2008213261A1PendingUtilityA1

Transdiscal administration of specific inhibitors of pro-inflammatory cytokines

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Assignee: DIMAURO THOMAS MPriority: May 13, 2003Filed: Jul 30, 2007Published: Sep 4, 2008
Est. expiryMay 13, 2023(expired)· nominal 20-yr term from priority
A61K 47/34A61B 17/7061A61K 38/1875A61K 39/395A61K 38/18A61K 39/3955A61K 38/17A61K 9/0012A61K 38/20A61K 9/0019C12Y 304/21005A61K 9/0085A61K 38/1841G01N 33/6869G01N 2333/54A61K 35/32A61K 38/1793A61K 38/363A61K 45/06A61K 35/28A61K 38/4833A61P 19/00
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Claims

Abstract

The present invention relates to injecting a high specificity cytokine antagonist into a diseased intervertebral disc.

Claims

exact text as granted — not AI-modified
1 . A formulation for treating degenerative disc disease, comprising:
 a) a high specificity cytokine antagonist, and   b) a second therapeutic agent selected from the group consisting of:
 i) a growth factor, and 
 ii) viable cells, 
   wherein the high specificity cytokine antagonist inhibits tumor necrosis factor-alpha (TNF-α).   
     
     
         2 . The formulation of  claim 1  wherein the second therapeutic agent is viable cells. 
     
     
         3 . The formulation of  claim 2  wherein the viable cells comprise mesenchymal stem cells. 
     
     
         4 . The formulation of  claim 3  wherein the mesenchymal stem cells are autologous. 
     
     
         5 . The formulation of  claim 4  wherein the mesenchymal stem cells are provided in a concentrated form. 
     
     
         6 . The formulation of  claim 1  wherein the second therapeutic agent is a growth factor. 
     
     
         7 . The formulation of  claim 6  wherein the growth factor is transforming growth factor (TGF-β) or a bone morphogenetic protein (BMP). 
     
     
         8 . The formulation of  claim 1  wherein the antagonist is a monoclonal antibody that inhibits TNF-α. 
     
     
         9 . The formulation of  claim 8  wherein the monoclonal antibody is infliximab. 
     
     
         10 . The formulation of  claim 1  wherein the antagonist is etanercept. 
     
     
         11 . The formulation of  claim 1  wherein the high specificity cytokine antagonist is present in the formulation in a concentration of at least 100 mg/ml.

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