US2003021828A1PendingUtilityA1

Method for treating and/or preventing retinal diseases with substained release corticosteroids

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Assignee: CONTROL DELIVERY SYSTEMSPriority: Mar 22, 1999Filed: Sep 25, 2002Published: Jan 30, 2003
Est. expiryMar 22, 2019(expired)· nominal 20-yr term from priority
A61P 9/00A61P 35/00A61K 9/0051A61K 31/573A61P 27/02
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Claims

Abstract

The present invention relates to a method for administering a corticosteroid to a posterior segment of an eye. In the method, a sustained release device is implanted to deliver the corticosteroid to the eye. The aqueous corticosteroid concentration remains less than vitreous corticosteroid concentration during release of the corticosteroid from the device.

Claims

exact text as granted — not AI-modified
What is claimed is:  
     
         1 . A method for administering a corticosteroid to a posterior segment of an eye, the method comprising the step of: 
 implanting a sustained release device to deliver the corticosteroid to the vitreous of the eye and wherein aqueous corticosteroid concentration is less than vitreous corticosteroid concentration during release.    
     
     
         2 . A method according to  claim 1 , wherein aqueous corticosteroid concentration is about 0.002 μg/ml to about 0.01 μg/ml.  
     
     
         3 . A method according to  claim 2 , wherein aqueous corticosteroid concentration is about 0.01 μg/ml to about 0.05 μg/ml.  
     
     
         4 . A method according to  claim 1 , wherein aqueous corticosteroid concentration is non-toxic and is less than 0.05 μg/ml.  
     
     
         5 . A method according to  claim 1 , wherein the device releases corticosteroid for about 1 month to about 10 years.  
     
     
         6 . A method according to  claim 5 , wherein the device releases corticosteroid for about 6 months to about 5 years  
     
     
         7 . A method according to  claim 1 , wherein the vitreous corticosteroid concentration is therapeutic.  
     
     
         8 . A method according to  claim 1 , wherein the vitreous corticosteroid concentration is less than about 10 μg/ml.  
     
     
         9 . A method according to  claim 1 , wherein the corticosteroid is selected from the group consisting of triamcinolone, dexamethasone, fluocinolone, cortisone, prednisolone, flumetholone, and derivatives thereof.  
     
     
         10 . A method according to  claim 1 , comprising intravitreally implanting the sustained release device.  
     
     
         11 . A method according to  claim 1 , wherein a disease state to be treated is selected from the group consisting of ocular neovascularization, ocular inflammation and retinal degeneration.  
     
     
         12 . A method according to  claim 1 , wherein the sustained release device releases the corticosteroid with pseudo zero order kinetics.  
     
     
         13 . A method according to  claim 1 , wherein the sustained release device has a mean release rate of about 1 μg/day to about 50 μg/day of corticosteroid.  
     
     
         14 . A method according to  claim 13 , wherein sustained release device has a mean release rate of about 1 μg/day to about 10 μg/day of corticosteroid.  
     
     
         15 . A method according to  claim 1 , wherein the sustained release device releases only one drug.  
     
     
         16 . An implantable, sustained release device for administering a corticosteroid to a posterior segment of an eye, the device comprising: 
 a corticosteroid, wherein the device is configured to provide sustained release of the corticosteroid to the vitreous of the eye such that aqueous corticosteroid concentration remains less than vitreous corticosteroid concentration during the release.

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