US2015087647A1PendingUtilityA1

Combination of brimonidine and timolol for topical ophthalmic use

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Assignee: ALLERGAN SALES LLCPriority: Apr 19, 2002Filed: Apr 28, 2014Published: Mar 26, 2015
Est. expiryApr 19, 2022(expired)· nominal 20-yr term from priority
A61P 27/00A61P 27/04A61K 45/06A61K 31/535A61K 9/08A61K 31/498A61K 31/5377A61K 31/4168A61K 9/0048A61K 47/02F21V 23/023F21V 23/004A61P 27/06A61P 27/02G02B 6/0073F21V 23/002
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Claims

Abstract

Disclosed are pharmaceutical compositions comprising brimonidine and timolol for topical ophthalmic delivery and a method of treatment comprising administering said composition when indicated for glaucoma and associated conditions such as elevated intraocular pressure in the eyes of humans.

Claims

exact text as granted — not AI-modified
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         17 . A method of reducing the adverse events experienced by a patient taking brimonidine comprising administering twice daily to the affected eye of the patient a single composition comprising 0.2% w/v brimonidine tartrate and 0.5% w/v timolol free base, wherein said method reduces the incidence of one or more adverse events, as compared to the administration of 0.2% w/v brimonidine tartrate monotherapy three times per day. 
     
     
         18 . The method of  claim 17 , wherein the adverse event is conjunctival hyperemia. 
     
     
         19 . The method of  claim 17 , wherein the adverse event is oral dryness. 
     
     
         20 . The method of  claim 17 , wherein the adverse event is eye pruritus. 
     
     
         21 . The method of  claim 17 , wherein the adverse event is allergic conjunctivitis. 
     
     
         22 . The method of  claim 17 , wherein the adverse event is foreign body sensation. 
     
     
         23 . The method of  claim 17 , wherein the adverse event is conjunctival folliculosis 
     
     
         24 . The method of  claim 17 , wherein the adverse event is somnolence.

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