US2022096523A1PendingUtilityA1
Compositions for the treatment of dry eye
Est. expiryOct 6, 2031(~5.2 yrs left)· nominal 20-yr term from priority
A61K 9/0048A61K 47/38A61K 47/32A61K 47/26A61K 47/10A61K 33/22A61K 31/205A61P 27/02A61K 31/745A61K 31/34A61P 27/04A61K 31/717A61K 36/47A61K 31/047A61K 9/00
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Claims
Abstract
The present invention relates to ophthalmic compositions and methods useful to treat dry eye, or to diagnose, cure, mitigate, treat, or prevent dry eye syndrome in man or other animals.
Claims
exact text as granted — not AI-modifiedWhat is claimed is:
1 . An ophthalmic composition comprising polyoxyethylene (80) sorbitan monooleate, carboxymethylcellulose sodium, glycerin, boric acid, acrylates/C10-30 alkyl acrylate crosspolymer, castor oil, erythritol, levocarnitine, sodium hydroxide, and water.
2 . The composition of claim 1 , wherein the polyoxyethylene (80) sorbitan monooleate is present at a concentration of about 0.1% w/w to about 2% w/w.
3 . The composition of claim 1 wherein the carboxymethylcellulose sodium is present at a concentration of about 0.1 w/w to about 2% w/w.
4 . The composition of claim 1 , wherein the glycerin is present at a concentration of about 0.2% w/w to about 5% w/w.
5 . The composition of claim 1 , wherein the boric acid is present at a concentration of about 0.02% to about 2% w/w.
6 . The composition of claim 1 , wherein the acrylates/C10-30 alkyl acrylate crosspolymer is present at a concentration of about 0.02% to about 0.5% w/w.
7 . The composition of claim 1 , wherein the castor oil is present at a concentration of about 0.05% to about 0.5% w/w.
8 . The composition of claim 1 , wherein the erythritol is present at a concentration of about 0.05% or about 3% w/w.
9 . The composition of claim 1 , wherein the levocarnitine is present at a concentration of about 0.05% or about 3% w/w.
10 . The composition of claim 1 , wherein the pH is about 7.3.
11 . The composition of claim 1 , comprising about 0.5% w/w polyoxyethylene (80) sorbitan monooleate, about 0.5% w/w carboxymethylcellulose sodium, about 1.0% w/w glycerin, about 0.6% w/w boric acid, about 0.1% w/w acrylates/C10-30 alkyl acrylate crosspolymer, about 0.25% w/w castor oil, about 0.25% w/w erythritol, about 0.25% w/w levocarnitine, sodium hydroxide, a pH of about 7.3 and water.
12 . A method of treating, diagnosing, curing, mitigating or preventing dry eye syndrome comprising administering an effective amount of an ophthalmic composition according to claim 1 to an eye of a man or other animal in need thereof.
13 . The method according to claim 12 , wherein the ophthalmic composition comprises about 0.5% w/w polyoxyethylene (80) sorbitan monooleate, about 0.5% w/w carboxymethylcellulose sodium, about 1.0% w/w glycerin, about 0.6% w/w boric acid, about 0.1% w/w acrylates/C10-30 alkyl acrylate crosspolymer, about 0.25% w/w castor oil, about 0.25% w/w erythritol, about 0.25% w/w levocarnitine, sodium hydroxide, a pH of about 7.3 and water.
14 . The composition of claim 1 , further comprising stabilized oxychloro complexes.
15 . The composition of claim 14 , wherein the stabilized oxychloro complex is present at a concentration of about 0.002% or about 0.05% w/w.
16 . The ophthalmic composition of claim 11 , further comprising about 0.01% w/w of stabilized oxychloro complexes.
17 . A method of treating, diagnosing, curing, mitigating or preventing dry eye syndrome comprising administering an effective amount of an opthalmic composition according to claim 14 to an eye of a man or other animal in need thereof.
18 . The method according to claim 17 , wherein the ophthalmic composition comprises about 0.5% w/w polyoxyethylene (80) sorbitan monooleate, about 0.5% w/w carboxymethylcellulose sodium, about 1.0% w/w glycerin, about 0.01% w/w of stabilized oxychloro complexes, about 0.6% w/w boric acid, about 0.1% w/w acrylates/C10-30 alkyl acrylate crosspolymer, about 0.25% w/w Castor Oil, about 0.25% w/w erythritol, about 0.25% w/w levocarnitine, sodium hydroxide to obtain a pH of about 7.3 and water.Join the waitlist — get patent alerts
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