US2010104654A1PendingUtilityA1

Prostaglandin and prostamide drug delivery systems and intraocular therapeutic uses thereof

Assignee: ALLERGAN INCPriority: Oct 27, 2008Filed: Oct 27, 2008Published: Apr 29, 2010
Est. expiryOct 27, 2028(~2.3 yrs left)· nominal 20-yr term from priority
A61P 27/06A61K 9/204A61K 31/216A61K 9/0051A61K 31/557A61K 31/5575A61L 31/16A61K 9/0048A61L 31/06A61K 9/1647
65
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Claims

Abstract

Biocompatible, bioerodible implants and microspheres include latanoprost and a biodegradable polymer effective, when placed intraocular (such as into the subtenon space) to treat glaucoma.

Claims

exact text as granted — not AI-modified
1 . A pharmaceutical composition for intraocular use to treat an ocular condition, the composition comprising:
 (a) a plurality of microspheres made of a bioerodible polymer, and;   (a) a therapeutic agent selected from the group consisting of latanoprost, bimatoprost and travoprost and their salts, esters and derivatives, contained by the microspheres.   
   
   
       2 . The composition of  claim 3  wherein the microspheres comprise from about 1% to about 99% by weight of the polymer. 
   
   
       3 . The composition of  claim 2 , wherein the polymer is a PLGA. 
   
   
       4 . The composition of  claim 2  wherein the microspheres have an average greatest dimension in a range of from about 5 microns to about 1 mm. 
   
   
       5 . The composition of  claim 4  wherein the microspheres has a mean diameter between about 15 microns and about 55 microns. 
   
   
       6 . The method of  claim 5  wherein the therapeutic agent comprises from about 0.1% to about 90% by weight of the microspheres. 
   
   
       7 . The composition of  claim 6  wherein the microspheres comprise between about 8 to 15 weight % latanoprost. 
   
   
       8 . The composition of  claim 1  further comprising a high viscosity hyaluronic acid. 
   
   
       9 . The composition of  claim 1  wherein the ocular condition is glaucoma. 
   
   
       10 . A pharmaceutical composition for intraocular use to treat glaucoma, the composition comprising:
 (a) a plurality of microspheres made from a PLGA;   (b) latanoprost contained by the microspheres, and;   (c) a high viscosity hyaluronic acid.   
   
   
       11 . A pharmaceutical composition for intraocular use to treat glaucoma, the composition comprising:
 (a) a sustained release implant made from a PLGA polymer, a PLA polymer, and a PEG co-solvent, and;   (b) latanoprost contained by the implant, wherein the implant comprises about 30 weight percent latanoprost and the implant can release the latanoprost over a period of time of at least 70 days.   
   
   
       12 . A method of treating glaucoma, the method comprising intraocular administration to a patient with glaucoma of a pharmaceutical composition comprising:
 (a) a plurality of microspheres made from a PLGA and/or PLA;   (b) latanoprost contained by the microspheres, and;   (c) a high viscosity hyaluronic acid, thereby treating the glaucoma.   
   
   
       13 . The method of  claim 12 , wherein the microspheres can release the latanoprost for at least about one week after the administration step. 
   
   
       14 . The method of  claim 13 , wherein the microspheres can release the latanoprost for at least about one month after the administration step. 
   
   
       15 . The method of  claim 14 , wherein the microspheres can release the latanoprost for at least about two months after the administration step. 
   
   
       16 . The method of  claim 15 , wherein the microspheres can release the latanoprost for at least about three months after the administration step. 
   
   
       17 . The method of  claim 16 , wherein the microspheres can release the latanoprost for at least about four months after the administration step. 
   
   
       18 . The method of  claim 17 , wherein the microspheres can release the latanoprost for at least about six months after the administration step. 
   
   
       19 . The method of  claim 14 , wherein the microspheres can release the latanoprost for between about one month and about six months after the administration step. 
   
   
       20 . The method of  claim 12 , the intraocular administration step is carried out by injection into the sub-tenon space. 
   
   
       21 . The method of  claim 20 , the sub tenon administration step is carried out injection into the anterior sub-tenon space. 
   
   
       22 . The method of  claim 12 , wherein the pharmaceutical composition treats glaucoma by reducing baseline intraocular pressure by up to 45%. 
   
   
       23 . A method of treating glaucoma, the method comprising anterior sub-tenon administration to a patient with glaucoma of a pharmaceutical composition comprising:
 (a) a plurality of microspheres made from a PLGA and/or PLA;   (b) latanoprost contained by the microspheres, wherein the microspheres release the latanoprost for at least about two months after the administration step, and;   (c) a high viscosity hyaluronic acid, thereby treating the glaucoma by reducing baseline intraocular pressure by up to about 45%.

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