US2015087647A1PendingUtilityA1
Combination of brimonidine and timolol for topical ophthalmic use
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
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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.Cited by (0)
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