IP Library Granted Patent US 8,147,823
Granted Patent B2
US 8,147,823 · App. 12/832,282 · Granted Apr 3, 2012

Method of treating or retarding the development of blindness

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Quick Facts
Patent No.
US 8,147,823
App. No.
12/832,282
Granted
Apr 3, 2012
Kind
B2
Abstract

A method for treating an ocular disorder characterized by the defect or absence of a normal gene in the ocular cells of a human or animal subject involves administering to the subject by subretinal injection an effective amount of a recombinant adeno-associated virus carrying a nucleic acid sequence encoding the normal gene under the control of a promoter sequence which expresses the product of the gene in the ocular cells. The ocular cells are preferably retinal pigment epithelial (RPE) cells, and the gene is preferably an RPE-specific gene, e.g., RPE65. The promoter is one that can express the gene product in the RPE cells. Compositions for subretinal administration are useful in this method.

Claims (9)

1. A method for treating a human subject having Leber Congenital Amaurosis, the method comprising:

administering to the subject by subretinal injection a recombinant adeno-associated virus (rAAV) comprising a nucleic acid sequence encoding a normal retinal pigment specific epithelial 65 (RPE65) gene operably linked to a chicken beta actin promoter/CMV enhancer, wherein said rAAV is administered in a dosage of from 1×10 9 to 2×10 12 rAAV in a volume comprising about 150 microliters, thereby restoring visual function in said subject.

2. The method according to claim 1 , wherein said rAAV is administered in a volume comprising about 250 microliters.

3. The method according to claim 1 , wherein said rAAV is administered in a volume of between 150 to 800 microliters.

4. The method according to claim 1 , wherein said rAAV is administered in a volume comprising of between 250 to 500 microliters.

5. The method according to claim 1 , wherein said rAAV is administered in a volume comprising about 500 microliters.

6. The method according to claim 1 , wherein said rAAV is administered in a volume comprising about 800 microliters.

7. The method according to claim 1 , wherein said rAAV is administered in a dosage of from 1×10 10 to 2×10 11 rAAV in a volume of between 250 to 500 microliters.

8. The method according to claim 1 , wherein said ocular cells are retinal pigment epithelial cells.

Assignments (2)
CONFIRMATORY LICENSE Recorded Nov 10, 2022
From: UNIVERSITY OF PENNSYLVANIA
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 061916/0393 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 28, 2012
From: JACOBSON, SAMUEL G
To: THE TRUSTEES OF THE UNIVERSITY OF PENNSYLVANIA
Reel/Frame 027772/0206 →