IP Library Granted Patent US 8,492,141
Granted Patent B2
US 8,492,141 · App. 12/766,741 · Granted Jul 23, 2013

Neostatins

Inventors: Dimitri T. Azar (Chicago, IL); Jin-Hong Chang (Clarendon Hills, IL)
Assignee: Massachusetts Eye & Ear Infirmary
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Quick Facts
Patent No.
US 8,492,141
App. No.
12/766,741
Granted
Jul 23, 2013
Kind
B2
Abstract

The invention provides fragments of type XVIII collagen termed neostatins, and methods for their use in the treatment of opthalmological disorders associated with angiogenesis.

Claims (13)

1. A method of inhibiting or delaying progression of corneal neovascularization associated with increased levels of bFGF in a patient, the method comprising administering to the eye of the patient a therapeutically effective amount of a composition comprising an expression vector comprising an isolated nucleic acid molecule encoding the polypeptide of SEQ ID NO:2 or 4, operatively linked to a promoter, wherein expression of said polypeptide results in inhibition or delaying of the progression of bFGF-associated corneal neovascularization.

2. A method of inhibiting or delaying progression of corneal neovascularization associated with increased levels of bFGF in a patient, the method comprising administering to the eye of the patient a therapeutically effective amount of a composition comprising an expression vector comprising a nucleic acid molecule encoding a fusion protein, wherein the fusion protein comprises amino acid sequence of SEQ ID NO:2 or 4 linked to a non-collagen XVIII amino acid sequence, the nucleic acid molecule is operatively linked to a promoter, and expression of said fusion protein results in inhibition or delaying of the progression of bFGF-associated corneal neovascularization.

3. The method of claim 1 , wherein the composition further comprises a pharmaceutically acceptable carrier.

4. The method of claim 2 , wherein the composition further comprises a pharmaceutically acceptable carrier.

5. The method of claim 1 , wherein the nucleic acid molecule encodes the polypeptide of ID NO:2.

6. The method of claim 1 , wherein the nucleic acid molecule encodes the polypeptide of ID NO:4.

7. The method of claim 2 , wherein the fusion protein comprises the polypeptide of SEQ ID NO:2.

8. The method of claim 2 , wherein the fusion protein comprises the polypeptide of SEQ ID NO:4.

9. A method of inhibiting or delaying progression of corneal neovascularization associated with increased levels of bFGF during wound healing in a patient, the method comprising administering to the eye of the patient a therapeutically effective amount of a composition comprising an expression vector comprising an isolated nucleic acid molecule encoding the polypeptide of SEQ ID NO:2 or 4, operatively linked to a promoter, wherein expression of said polypeptide results in inhibition or delaying of the progression of corneal neovascularization of bFGF-associated corneal neovascularization during wound healing.

10. The method of claim 9 , wherein the composition further comprises a pharmaceutically acceptable carrier.

11. The method of claim 9 , wherein the nucleic acid molecule encodes the polypeptide of SEQ ID NO:2.

12. The method of claim 9 , wherein the nucleic acid molecule encodes the polypeptide of SEQ ID NO:4.

13. The method of claim 9 , wherein the wound is a surgical wound.

Assignments (2)
CONFIRMATORY LICENSE Recorded Mar 2, 2023
From: MASSACHUSETTS EYE AND EAR INFIRMARY
To: NATIONAL INSTITUTES OF HEALTH - DIRECTOR DEITR
Reel/Frame 062851/0042 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 23, 2010
From: AZAR, DIMITRI T.; CHANG, JIN-HONG
To: MASSACHUSETTS EYE & EAR INFIRMARY
Reel/Frame 025032/0530 →
Continuity (4)
Continuation 11965411 · Dec 27, 2007
Division 11346490 · Feb 1, 2006
Provisional Application 60649029 · Feb 1, 2005
Related Publication 20100331396A1 · Dec 30, 2010