IP Library › Granted Patent US 10,300,057
Granted Patent B2
US 10,300,057 · App. 15/142,087 · Granted May 28, 2019

Compositions and methods for treating retinal degradation

Inventors: Jayakrishna Ambati (Lexington, KY); Benjamin Fowler (Lexington, KY)
Assignee: University of Kentucky Research Foundation
A61K31/506A61K31/513A61K31/52A61K31/706A61K31/7052A61K31/7064A61K31/7068A61K31/7072A61K31/7076C07D405/04C07D411/04
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Quick Facts
Patent No.
US 10,300,057
App. No.
15/142,087
Granted
May 28, 2019
Kind
B2
Abstract

The present disclosure relates to compositions and methods for treating retinal damage and/or retinal degradation. More specifically, this disclosure relates to methods for treating degradation of the retinal pigment epithelium by administering compositions comprising a nucleoside and/or a nucleoside or nucleotide reverse transcriptase inhibitor.

Claims (34)

1. A method for treating rheumatoid arthritis, comprising:

administering an effective amount of a composition to a subject in need thereof, wherein the composition comprises a pharmaceutically acceptable carrier and a compound selected from:

(i) a compound having the structure of

or a pharmaceutically acceptable salt thereof;

(ii) a compound having the structure of

or a pharmaceutically acceptable salt thereof;

(iii) stavudine (d4T);

(iv) azidothymidine (AZT);

(v) abacavir (ABC); and

(vi) a combination thereof.

2. The method of claim 1 , comprising inhibiting inflammasome activation by Alu RNA associated with a cell.

3. The method of claim 1 , comprising reducing ATP-induced permeability of a cell.

4. The method of claim 1 , comprising reducing an amount of mitochondrial reactive oxygen species in a cell.

5. The method of claim 2 , wherein the inflammasome is selected from an NLRP3 inflammasome, an IL-1beta inflammasome, and a combination thereof.

6. A method for treating diabetes, comprising:

administering an effective amount of a composition to a subject in need thereof, wherein the composition comprises a pharmaceutically acceptable carrier and a compound selected from:

(i) a compound having the structure of

or a pharmaceutically acceptable salt thereof;

(ii) a compound having the structure of

or a pharmaceutically acceptable salt thereof;

(iii) stavudine (d4T);

(iv) lamivudine (3TC);

(v) cordycepin;

(vi) azidothymidine (AZT);

(vii) abacavir (ABC); and

(viii) a combination thereof.

7. The method of claim 6 , comprising inhibiting inflammasome activation by Alu RNA associated with a cell.

8. The method of claim 7 , wherein the inflammasome is selected from an NLRP3 inflammasome, an IL-1beta inflammasome, and a combination thereof.

9. The method of claim 6 , comprising reducing ATP-induced permeability of a cell.

10. The method of claim 6 , comprising reducing an amount of mitochondrial reactive oxygen species in a cell.

11. The method of claim 6 , wherein the diabetes is type 2 diabetes.

12. The method of claim 1 , wherein the compound is selected from (i), (iii), (iv), and (v).

13. The method of claim 1 , wherein the compound is selected from (i) and (ii).

14. The method of claim 1 , wherein the compound is (i).

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 13, 2016
From: AMBATI, JAYAKRISHNA; FOWLER, BENJAMIN
To: UNIVERSITY OF KENTUCKY RESEARCH FOUNDATION
Reel/Frame 038900/0610 →
Continuity (4)
Continuation 14450000 · Aug 1, 2014
Provisional Application 61861290 · Aug 1, 2013
Provisional Application 61987612 · May 2, 2014
Related Publication 20160263114A1 · Sep 15, 2016
Cited By (1)
US 12,274,701