IP Library › Granted Patent US 11,197,937
Granted Patent B2
US 11,197,937 · App. 16/093,420 · Granted Dec 14, 2021

Compositions for treatment of wet age-related macular degeneration

Inventors: Anna P. Tretiakova (Woburn, MA); James M. Wilson (Philadelphia, PA)
Assignee: The Trustees of the University of Pennsylvania
A61K48/0075A61K9/0019A61K9/0048A61K9/10A61K35/761A61K48/005C07K16/22C12N15/86C07K2317/55C07K2319/33C12N2750/14143
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Quick Facts
Patent No.
US 11,197,937
App. No.
16/093,420
Granted
Dec 14, 2021
Kind
B2
Abstract

A recombinant adeno-associated virus (rAAV) having an AAV8 capsid which is suitable for intra-retinal injection is provided herein. The rAAV comprises a vector genome packaged within the capsid which contains, operably linked to regulatory elements which direct expression of anti-human vascular endothelial growth factor (VEGF) antigen binding antibody fragment (aVEGF), a coding sequence for aVEGF, wherein the coding sequence is operably linked to regulatory elements which direct expression of the anti-VEGF Fab in the eye. Also provided herein are liquid suspensions containing these rAAV8.aVEGF and methods of using same for treatment of wet AMD and other ocular conditions.

Claims (5)

1. A recombinant adeno-associated virus (rAAV) having an AAV8 capsid, wherein the rAAV comprises a vector genome packaged within the capsid, wherein the vector genome comprises a 5′ AAV-2 inverted terminal repeat, an expression cassette consisting of the contiguous nucleotides 198 to 3733 of SEQ ID NO: 14, and a 3′ AAV-2 inverted terminal repeat.

2. A liquid suspension suitable for sub-retinal and/or intra-retinal injection, said suspension comprising an aqueous liquid and the recombinant adeno-associated virus (rAAV) according to claim 1 and optionally one or more excipients, preservatives, and/or surfactants.

3. A product comprising: (a) a first container comprising the rAAV according to claim 1 and an aqueous liquid, (b) optionally a second container comprising a diluent, and (c) a needle for injection.

4. The suspension according to claim 2 , wherein the suspension comprises about 1×10 11 genome copies (GC)/mL to about 1×10 13 GC/mL of the rAAV.

5. The suspension according to claim 2 , wherein the suspension volume is about 10 μL to about 300 μL.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 12, 2019
From: WILSON, JAMES M.; TRETIAKOVA, ANNA P.
To: THE TRUSTEES OF THE UNIVERSITY OF PENNSYLVANIA
Reel/Frame 049742/0381 →
Continuity (6)
Provisional Application 62466721 · Mar 3, 2017
Provisional Application 62460515 · Feb 17, 2017
Provisional Application 62442946 · Jan 5, 2017
Provisional Application 62331100 · May 3, 2016
Provisional Application 62323184 · Apr 15, 2016
Related Publication 20190381194A1 · Dec 19, 2019
Cited By (2)
US 12,275,960 US 12,365,726