US2013303625A1PendingUtilityA1
Agent for the prevention, improvement or treatment of retinal disease
Est. expiryFeb 27, 2032(~5.6 yrs left)· nominal 20-yr term from priority
A61P 27/06A61K 47/26A61K 47/44A61K 9/0048A61K 47/02A61K 31/121A61K 9/0053A61K 45/06A61P 27/02
45
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Claims
Abstract
A prophylactic, ameliorating or therapeutic agent for a retinal disease, the agent comprising geranylgeranylacetone which (a) is a mixture of (5E,9E,13E)-geranylgeranylacetone and (5Z,9E,13E)-geranylgeranylacetone, the (5E,9E,13E)-geranylgeranylacetone content of the mixture being 80% by weight or more, (b) consists of (5E,9E,13E)-geranylgeranylacetone, or (c) consists of (5Z,9E,13E)-geranylgeranylacetone directly suppresses the death of a retinal cell, thereby fundamentally preventing, ameliorating or treating the retinal disease.
Claims
exact text as granted — not AI-modified1 . A method for preventing, ameliorating or treating a retinal disease, the method comprising the step of administering to a patient with a retinal disease an effective amount of geranylgeranylacetone which
(a) is a mixture of (5E,9E,13E)-geranylgeranylacetone and (5Z,9E,13E)-geranylgeranylacetone, the (5E,9E,13E)-geranylgeranylacetone content of the mixture being 80% by weight or more, (b) consists of (5E,9E,13E)-geranylgeranylacetone, or (c) consists of (5Z,9E,13E)-geranylgeranylacetone, thereby preventing, ameliorating or treating the retinal disease.
2 . The method according to claim 1 , comprising administering an ophthalmic composition comprising geranylgeranylacetone to the eye of a patient with a retinal disease.
3 . The method according to claim 2 , wherein the geranylgeranylacetone content of the ophthalmic composition is 0.00001 to 10% by weight relative to the total amount of the preparation.
4 . The method according to claim 1 , comprising orally administering an oral agent comprising geranylgeranylacetone to a patient with a retinal disease.
5 . The method according to claim 4 , wherein the geranylgeranylacetone content of the oral agent is 0.001 to 80% by weight relative to the total amount of the preparation.
6 . The method according to claim 1 , wherein the retinal disease is a disease selected from the group consisting of glaucoma, retinitis pigmentosa, age-related macular degeneration and diabetic retinopathy.
7 . A method for protecting a retinal cell, the method comprising the step of administering to a patient with a retinal disease an effective amount of geranylgeranylacetone which
(a) is a mixture of (5E,9E,13E)-geranylgeranylacetone and (5Z,9E,13E)-geranylgeranylacetone, the (5E,9E,13E)-geranylgeranylacetone content of the mixture being 80% by weight or more, (b) consists of (5E,9E,13E)-geranylgeranylacetone, or (c) consists of (5Z,9E,13E)-geranylgeranylacetone, thereby protecting a retinal cell.
8 . The method according to claim 7 , comprising administering an ophthalmic composition comprising geranylgeranylacetone to the eye of a patient with a retinal disease.
9 . The method according to claim 8 , wherein the geranylgeranylacetone content of the ophthalmic composition is 0.00001 to 10% by weight relative to the total amount of the preparation.
10 . The method according to claim 7 , comprising orally administering an oral agent comprising geranylgeranylacetone to a patient with a retinal disease.
11 . The method according to claim 10 , wherein the geranylgeranylacetone content of the oral agent is 0.001 to 80% by weight relative to the total amount of the preparation.
12 . The method according to claim 7 , wherein the retinal disease is a disease selected from the group consisting of glaucoma, retinitis pigmentosa, age-related macular degeneration and diabetic retinopathy.
13 . A method for suppressing the degeneration, impairment or destruction of a retinal cell, the method comprising the step of administering to a patient with a retinal disease an effective amount of geranylgeranylacetone which
(a) is a mixture of (5E,9E,13E)-geranylgeranylacetone and (5Z,9E,13E)-geranylgeranylacetone, the (5E,9E,13E)-geranylgeranylacetone content of the mixture being 80% by weight or more, (b) consists of (5E,9E,13E)-geranylgeranylacetone, or (c) consists of (5Z,9E,13E)-geranylgeranylacetone, thereby suppressing the degeneration, impairment or destruction of a retinal cell.
14 . The method according to claim 13 , comprising administering an ophthalmic composition comprising geranylgeranylacetone to the eye of a patient with a retinal disease.
15 . The method according to claim 14 , wherein the geranylgeranylacetone content of the ophthalmic composition is 0.00001 to 10% by weight relative to the total amount of the preparation.
16 . The method according to claim 13 , comprising orally administering an oral agent comprising geranylgeranylacetone to a patient with a retinal disease.
17 . The method according to claim 16 , wherein the geranylgeranylacetone content of the oral agent is 0.001 to 80% by weight relative to the total amount of the preparation.
18 . The method according to claim 13 , wherein the retinal disease is a disease selected from the group consisting of glaucoma, retinitis pigmentosa, age-related macular degeneration and diabetic retinopathy.Join the waitlist — get patent alerts
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