US2019255065A1PendingUtilityA1
Ophthalmic compositions of rifamycins and uses thereof
Est. expiryJul 21, 2034(~8 yrs left)· nominal 20-yr term from priority
Inventors:Hiroaki Serizawa
A61P 27/02A61P 25/00A61K 47/02A61K 9/0019A61K 47/26A61K 9/0048A61K 31/5383A61K 47/14A61K 31/496A61K 31/435A61K 9/08A61K 47/10A61K 47/183
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Claims
Abstract
Provided herein are ophthalmic pharmaceutical formulations comprising a rifamycin compound. Also provided herein are methods of treating ocular diseases or disorders by administering such ophthalmic formulations.
Claims
exact text as granted — not AI-modified1 . A method of treating an ocular disease, disorder or condition resulting from neovascularization comprising topically administering to a patient in need thereof a pharmaceutically acceptable ophthalmic ointment composition comprising:
an effective amount of a rifamycin compound selected from the group consisting of rifampicin, rifabutin, rifapentine and rifaximin, or a pharmaceutically acceptable salt thereof and one or more pharmaceutically acceptable viscosity inducing agent.
2 . The method of claim 1 , wherein the ocular disease, disorder or condition is selected from age related macular degeneration (AMD), ocular neovascularization, or retinal ganglion cell injury.
3 . The method of claim 2 , wherein the ocular neovascularization comprises retinal neovascularization.
4 . A method of inhibiting ocular neovascularization in a retina of a patient in need thereof, comprising administering topically a pharmaceutically acceptable ophthalmic ointment composition comprising up to about 1% (w/v) of rifampicin, and one or more pharmaceutically acceptable viscosity inducing agent to an eye of the patient.
5 . The method of claim 4 , wherein the pharmaceutically acceptable ophthalmic ointment composition comprises from about 0.1% to about 1% of rifampicin.
6 . The method of claim 4 , wherein the pharmaceutically acceptable ophthalmic ointment composition comprises from about 0.25% to about 1% of rifampicin.
7 . The method of claim 4 , wherein the pharmaceutically acceptable ophthalmic ointment composition comprises from about 0.5% to about 1% of rifampicin.
8 . The method of claim 4 , wherein the pharmaceutically acceptable ophthalmic ointment composition comprises from about 0.1% to about 0.5% of rifampicin.
9 . The method of claim 4 , wherein the pharmaceutically acceptable ophthalmic ointment composition comprises from about 0.25% to about 0.5% of rifampicin.
10 . The method of claim 4 , wherein the pharmaceutically acceptable ophthalmic ointment composition comprises from about 0.25% of rifampicin.
11 . The method of claim 4 , wherein the pharmaceutically acceptable ophthalmic ointment composition comprises from about 0.5% of rifampicin.
12 . The method of claim 1 , wherein the pharmaceutically acceptable ophthalmic ointment composition further comprises from about 0.1 wt %-10 wt % of a surfactant selected from polysorbate 80, tween 80, tween 20, polyoxyethylene hydrogenated castor oil, and lecithin, or combinations thereof.
13 . The method of claim 4 , wherein the pharmaceutically acceptable ophthalmic ointment composition further comprises about 0.1 wt %-10 wt % of a surfactant selected from polysorbate 80, tween 80, tween 20, polyoxyethylene hydrogenated castor oil, and lecithin, or combinations thereof.
14 . The method of claim 1 , wherein the one or more pharmaceutically acceptable viscosity inducing agent is selected from the group consisting of carboxyvinyl polymer, a cellulosic polymer, a polysaccharide, polyvinyl pyrrolidone, polyvinyl alcohol, and combinations thereof.
15 . The method of claim 4 , wherein the one or more pharmaceutically acceptable viscosity inducing agent is selected from the group consisting of carboxyvinyl polymer, a cellulosic polymer, a polysaccharide, polyvinyl pyrrolidone, polyvinyl alcohol, and combinations thereof.
16 . A method of inhibiting ocular neovascularization in a retina of a patient in need thereof, comprising administering topically a pharmaceutically acceptable ophthalmic ointment composition comprising from about 1% to about 10% (w/v) of rifampicin, and one or more pharmaceutically acceptable viscosity inducing agent to an eye of the patient.
17 . The method of claim 16 , comprising from about 1.5% to about 5% (w/v) of rifampicin.
18 . The method of claim 16 , comprising from about 2% to about 2.5% (w/v) of rifampicin.Join the waitlist — get patent alerts
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