US2012029475A1PendingUtilityA1

Drug Combinations Useful for Prevention of Restenosis

Individually held — no corporate assignee on recordPriority: May 12, 2000Filed: Sep 7, 2011Published: Feb 2, 2012
Est. expiryMay 12, 2020(expired)· nominal 20-yr term from priority
A61K 31/436A61F 2002/91541A61K 31/727A61F 2/91A61F 2250/0067A61L 2300/41A61F 2310/0097A61L 2300/606A61L 31/16A61L 2300/45A61L 2300/416A61F 2/915A61L 2300/43A61P 9/00A61K 45/06A61F 2250/0068
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Claims

Abstract

The current invention comprises an approach to solving the clinical problem of restenosis, which involves the administration of combinations of drugs to patients undergoing PTCA or stent implantation. In one embodiment of the invention, an antiproliferative agent such as rapamycin, vincristine or taxol is administered in combination with the anti-inflammatory agent, dexamethasone, to patients systemically, either subcutaneously or intravenously. In another embodiment of the invention, the antiproliferative and anti-inflammatory agents are bound in a single formulation to the surface of a stent by means of incorporation within either a biodegradeable or biostable polymeric coating. Alternatively, such drug combinations could be incorporated into a stent constructed with a grooved reservoir.

Claims

exact text as granted — not AI-modified
1 - 15 . (canceled) 
     
     
         16 . In combination:
 a catheter for the delivery of drugs to a blood vessel lumen of a patient; and   a therapeutic dosage amount of the combination of an anti-proliferative agent for inhibiting smooth muscle cell growth comprising rapamycin or an analogue thereof and an anti-inflammatory agent for inhibiting smooth muscle growth, both said agents contained in therapeutic dosage amounts.   
     
     
         17 . The combination of  claim 16  wherein the anti-inflammatory agent comprises dexamethasone. 
     
     
         18 . The combination of  claim 16  wherein the combination of at least two agents further includes a growth factor or cytokine signal transduction inhibitor. 
     
     
         19 . The combination of  claim 16  wherein the combination of at least two agents further includes a tyrosine kinase inhibitor. 
     
     
         20 . The combination of  claim 16  wherein the combination of at least two agents further includes an inhibitor of extracellular matrix synthesis. 
     
     
         21 . The combination of  claim 20  wherein the inhibitor of extracellular matrix synthesis comprises halofuginone and the anti-proliferative agent is taken from a group consisting of rapamycin, taxol, or vincristine.

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