IP Library Patent Application 12715853
Patent Application
App. No. 12/715,853

AGENTS FOR TREATMENT OF DIABETIC RETINOPATHY AND DRUSEN FORMATION IN MACULAR DEGENERATION

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Patent No.
US None
App. No.
12/715,853
Abstract

Agents that stimulate nuclear translocation of Nrf2 protein and the subsequent increases in gene products that detoxify and eliminate cytotoxic metabolites are provided in a method for treating diabetic retinopathy or drusen formation in age-related macular degeneration. The structurally diverse agents that act on the Nrf2/ARE pathway induce the expression of enzymes and proteins that possess chemically versatile cytoprotective properties and are a defense against toxic metabolites and xenobiotics. Agents include certain electrophiles and oxidants such as a Michael Addition acceptor, diphenol, thiocarbamate, quinone, 1,2-dithiole-3-thione, butylated hydroxyanisole, flavonoid other than genistein, an isothiocyanate, 3,5-di-tert-butyl-4-hydroxytoluene, ethoxyquin, a coumarin, combinations thereof, or a pharmacologically active derivative or analog thereof.

Claims (31)

1 . A method of preventing retinal vascular and neuronal damage due to diabetic retinopathy in a patient, said method comprising administering to said subject an effective amount of a composition comprising an agent capable of translocating Nrf2 protein to a retinal cell's nucleus wherein expression of gene products that detoxify and eliminate cytotoxic metabolites is activated, and an acceptable carrier,

wherein the agent comprises a Michael Addition acceptor, diphenol, thiocarbamate, quinone, 1,2-dithiole-3-thione, butylated hydroxyanisole, flavonoid other than genistein, an isothiocyanate, 3,5-di-tert-butyl-4-hydroxytoluene, ethoxyquin, a coumarin, or combinations thereof.

2 . The method of claim 1 , wherein the subject has symptoms of diabetic retinopathy.

3 . The method of claim 1 , wherein the agent comprises an isothiocyanate.

4 . The method of claim 3 , wherein the isothiocyanate comprises sulforaphane.

5 . The method of claim 1 , wherein the agent comprises a 1,2-dithiole-3-thione.

6 . The method of claim 5 , wherein the 1,2-dithiole-3-thione comprises oltipraz.

7 . The method of claim 1 , wherein the administering is by intraocular injection, implantation of a slow release delivery device, or topical, oral, or intranasal administration.

8 . The method of claim 1 , wherein the administering is by intraocular administration.

9 . A method of preventing retinal vascular and neuronal damage due to diabetic retinopathy in a subject, said method comprising diagnosing a subject with diabetic retinopathy, and

administering to said subject an effective amount of a composition comprising an agent capable of translocating Nrf2 protein to a retinal cell's nucleus wherein expression of gene products that detoxify and eliminate cytotoxic metabolites is activated, and an acceptable carrier,

wherein the agent comprises a Michael Addition acceptor, diphenol, thiocarbamate, quinone, 1,2-dithiole-3-thione, butylated hydroxyanisole, flavonoid other than genistein, an isothiocyanate, 3,5-di-tert-butyl-4-hydroxytoluene, ethoxyquin, a coumarin, or combinations thereof.

10 . A method of inhibiting subretinal drusen formation of a subject, the method comprising:

administering to the subject an effective amount of a composition comprising an agent having stimulatory activity for Nrf2 protein nuclear translocation, and an acceptable carrier,

wherein the agent comprises a Michael Addition acceptor, diphenol, thiocarbamate, quinone, 1,2-dithiole-3-thione, butylated hydroxyanisole, flavonoid, an isothiocyanate, 3,5-di-tert-butyl-4-hydroxytoluene, ethoxyquin, a coumarin, combinations thereof, or a pharmacologically active derivative or analog thereof.

11 . The method of claim 10 wherein the subject is at risk for developing subretinal drusen formation.

12 . The method of claim 10 wherein the subject has symptoms of developing subretinal drusen formation.

13 . The method of claim 10 wherein the agent comprises an isothiocyanate, or a pharmacologically active derivative thereof.

14 . The method of claim 13 wherein the isothiocyanate comprises sulforaphane, or a pharmacologically active derivative thereof.

15 . The method of claim 10 wherein the agent comprises a 1,2-dithiole-3-thione, or a pharmacologically active derivative thereof.

16 . The method of claim 15 wherein the 1,2-dithiole-3-thione comprises oltipraz, or a pharmacologically active derivative thereof.

17 . The method of claim 10 , wherein the administering is by intraocular injection, implantation of a slow release delivery device, or topical, oral, or intranasal administration.

18 . The method of claim 10 wherein the administering is by intraocular administration.

19 . A method of treatment for subretinal drusen formation of a subject, the method comprising:

diagnosing a subject with subretinal drusen formation, and

administering to the subject an effective amount of a composition comprising an agent having stimulatory activity for Nrf2 protein nuclear translocation, and an acceptable carrier,

wherein the agent comprises a Michael Addition acceptor, diphenol, thiocarbamate, quinone, 1,2-dithiole-3-thione, butylated hydroxyanisole, flavonoid, an isothiocyanate, 3,5-di-tert-butyl-4-hydroxytoluene, ethoxyquin, a coumarin, combinations thereof, or a pharmacologically active derivative or analog thereof.

20 . The method of claim 19 wherein the agent comprises a flavonoid other than genistein.

21 . The method of claim 20 wherein the agent comprises quercetin.

22 . The method of claim 19 wherein the agent comprises a flavonoid other than genistein.

23 . The method of claim 22 wherein the agent comprises quercetin.

Assignments (1)
MERGER Recorded May 31, 2011
From: ALCON, INC.
To: NOVARTIS AG
Reel/Frame 026376/0076 →