US2009156606A1PendingUtilityA1
Optical correction
Est. expiryDec 15, 2027(~1.4 yrs left)· nominal 20-yr term from priority
Inventors:Anant Sharma
A61P 27/02A61K 31/498A61K 31/138A61K 31/4168A61K 9/0048A61K 31/496A61K 31/216A61K 31/385A61K 31/4178A61K 31/222A61P 27/10
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Claims
Abstract
The present disclosure describes compositions which improve visual acuity and to methods for their use.
Claims
exact text as granted — not AI-modified1 . A medicament for topical administration to an eye comprising:
a first active agent comprising a parasympathetic agonist, and a second active agent selected from the group consisting of a sympathetic antagonist, a sympathetic agonist and combinations thereof.
2 . The medicament of claim 1 wherein the medicament comprises a form selected from the group consisting of a liquid, a gel, an ointment, and combinations thereof.
3 . The medicament of claim 1 wherein the parasympathetic agonist acts on acetylcholine receptors.
4 . The medicament of claim 1 wherein the parasympathetic agonist comprises pilocarpine.
5 . The medicament of claim 4 wherein the pilocarpine represents from about 0.05 to about 4%.
6 . The medicament of claim 1 wherein the sympathetic antagonist acts on a-receptors.
7 . The medicament of claim 1 wherein the sympathetic antagonist is selected from the group consisting of dapiprazole, thymoxamine, and combinations thereof.
8 . The medicament of claim 1 wherein the sympathetic antagonist comprises dapiprazole
9 . The medicament of claim 8 wherein the dapiprazole represents from about 0.05 to about 4%.
10 . The medicament of claim 1 wherein the sympathetic antagonist comprises thymoxamine.
11 . The medicament of claim 10 wherein the thymoxamine represents from about 0.05 to about 4%.
12 . The medicament of claim 1 wherein the sympathetic agonist is selected from the group consisting of brimonidine, iopidine, and combinations thereof.
13 . The medicament of claim 1 wherein the sympathetic antagonist comprises brimonidine.
14 . The medicament of claim 13 wherein the brimonidine represents from about 0.01 to about 4%.
15 . The medicament of claim 1 wherein the sympathetic antagonist comprises iopidne.
16 . A method for improving visual acuity comprising:
administering a first active agent comprising a parasympathetic agonist to an eye, and administering a second active agent selected from the group consisting of a sympathetic antagonist, a sympathetic agonist, and combinations thereof.
17 . The method of claim 16 wherein the parasympathetic agonist comprises pilocarpine.
18 . The method of claim 16 wherein the sympathetic antagonist is selected from the group consisting of dapiprazole, thymoxamine, and combinations thereof.
19 . The method of claim 16 wherein the sympathetic agonist is selected from the group consisting of brimonidine, iopidine, and combinations thereof.
20 . A method of improving visual acuity comprising:
administering a single composition comprising a first active agent and a second active agent to an eye, wherein the first and second active agents are selected from the group consisting of a parasympathetic agonist, sympathetic antagonist, a sympathetic agonist, and combinations thereof.
21 . The method of claim 20 wherein the parasympathetic agonist comprises pilocarpine.
22 . The method of claim 20 wherein the sympathetic antagonist is selected from the group consisting of dapiprazole, thymoxamine, and combinations thereof.
23 . The method of claim 20 wherein the sympathetic agonist is selected from the group consisting of brimonidine, iopidine, and combinations thereof.
24 . A method for treating an eye disorder comprising:
administering a first active agent comprising a parasympathetic agonist to an eye, and administering a second active agent selected from the group consisting of a sympathetic antagonist, a sympathetic agonist, and combinations thereof.
25 . The method of claim 24 wherein the eye disorder is selected from the group consisting of presbyopia, myopia, hypermetropia, astigmatism, and combinations thereof.
26 . The method of claim 24 wherein the parasympathetic agonist comprises pilocarpine.
27 . The method of claim 24 wherein the sympathetic antagonist is selected from the group consisting of dapiprazole, thymoxamine, and combinations thereof.
28 . The method of claim 24 wherein the sympathetic agonist is selected from the group consisting of brimonidine, iopidine, and combinations thereof.
29 . A method for treating an eye disorder comprising:
administering a single composition comprising a first active agent and a second active agent to an eye, wherein the first and second active agents are selected from the group consisting of a parasympathetic agonist, sympathetic antagonist, a sympathetic agonist, and combinations thereof
30 . The method of claim 29 wherein the eye disorder is selected from the group consisting of presbyopia, myopia, hypermetropia, astigmatism, and combinations thereof.
31 . The method of claim 30 wherein the parasympathetic agonist comprises pilocarpine.
32 . The method of claim 30 wherein the sympathetic antagonist is selected from the group consisting of dapiprazole, thymoxamine, and combinations thereof.
33 . The method of claim 30 wherein the sympathetic agonist is selected from the group consisting of brimonidine, iopidine, and combinations thereof.Join the waitlist — get patent alerts
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