US2013197047A1PendingUtilityA1
Ophthalmic compositions of parasympathetic stimulants and anti-inflammatories for use in the treatment of presbyopia
Est. expiryDec 18, 2026(~0.4 yrs left)· nominal 20-yr term from priority
Inventors:Jorge Luis Benozzi
A61P 43/00A61K 31/728A61K 33/38A61P 27/02A61K 31/4178A61K 31/60A61K 31/196A61K 33/08A61P 27/10A61K 31/232A61K 45/06A61K 31/17
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Claims
Abstract
Ophthalmic compositions for the treatment of presbyopia, including combinations of parasympathomimetics and non-steroidal anti-inflammatories.
Claims
exact text as granted — not AI-modified1 . A method of treating presbyopia comprising topically treating a patient in need thereof with a composition comprising a combination of a parasympathomimetic or a salt thereof and a non-steroidal anti-inflammatory drug or a salt thereof.
2 . The method of claim 1 , wherein the parasympathomimetic agent is pilocarpine or a salt thereof.
3 . The method of claim 2 , wherein the parasympathomimetic agent is pilocarpine hydrochloride.
4 . The method of claim 2 , wherein the non-steroidal anti-inflammatory drug is selected from a group consisting of diclofenac, ketorolac, bromfenac, flurbiprofen, suprofen, pranoprofen, oxyphenbutazone, bendazac, and indomethacin.
5 . The method of claim 4 , wherein the non-steroidal anti-inflammatory drug is diclofenac or a salt thereof.
6 . The method of claim 1 , wherein the non-steroidal anti-inflammatory drug is selected from a group consisting of diclofenac, ketorolac, bromfenac, flurbiprofen, suprofen, pranoprofen, oxyphenbutazone, bendazac, and indomethacin.
7 . The method of claim 6 , wherein the parasympathomimetic agent is pilocarpine hydrochloride.
8 . The method of claim 1 , wherein the composition comprises pilocarpine or a salt thereof in concentrations ranging from 1% to 2% and diclofenac or a salt thereof in an amount ranging from 0.1% to 0.5%.
9 . The method of claim 1 , wherein the parasympathomimetic agent or a salt thereof is 0.5% to 4% of the composition and the non-steroidal anti-inflammatory drug or a salt thereof is 0.01 mg to 0.1 mg of the composition.Join the waitlist — get patent alerts
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