IP Library Granted Patent US 9,340,594
Granted Patent B2
US 9,340,594 · App. 14/330,096 · Granted May 17, 2016

VEGF antagonist formulations for intravitreal administration

Inventors: Eric Furfine (Concord, MA); Daniel Dix (LaGrangeville, NY); Kenneth Graham (Pleasant Valley, NY); Kelly Frye (Mendham, NJ)
Assignee: REGENERON PHARMACEUTICALS, INC.
C07K14/47A61K9/0048A61K9/19A61K38/1793A61M5/178C07K14/4705C07K2319/30
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Quick Facts
Patent No.
US 9,340,594
App. No.
14/330,096
Granted
May 17, 2016
Kind
B2
Abstract

Ophthalmic formulations of a vascular endothelial growth factor (VEGF)-specific fusion protein antagonist are provided suitable for intravitreal administration to the eye. The ophthalmic formulations include a stable liquid formulation and a lyophilizable formulation. Preferably, the protein antagonist has an amino acid sequence of SEQ ID NO:4.

Claims (16)

1. A pre-filled syringe suitable for intravitreal administration comprising a 1 mL luer glass syringe fitted with a plunger and a stable ophthalmic formulation of a vascular endothelial growth factor (VEGF) trap, which consists of (i) a receptor component consisting essentially of an immunoglobulin-like domain 2 of a first VEGF receptor and an immunoglobulin-like domain 3 of a second VEGF receptor, and (ii) a multimerizing component, wherein the stable ophthalmic formulation comprises:

(a) 1-100 mg/ml a VEGF antagonist;

(b) 0.01-5% of one or more organic co-solvent;

(c) 5-40 mM of buffer; and

(d) optionally comprising 1.0-7.5% of a stabilizing agent.

2. The pre-filled syringe of claim 1 , wherein the first VEGF receptor is Flt1, and the second VEGF receptor is Flk1 or Flt4.

3. The pre-filled syringe according to claim 2 , wherein the VEGF trap is stable for at least 4 months.

4. The pre-filled syringe according to claim 3 , wherein the VEGF trap consists of amino acids 27-457 of SEQ ID NO:4.

5. The pre-filled syringe according to claim 4 , wherein the stable ophthalmic formulation comprises 40 mg/mL of the VEGF trap, 10 mM phosphate, 40 mM NaCI, 0.03% polysorbate 20, 5% sucrose, at pH 6.2-6.4.

6. The pre-filled syringe of claim 3 , wherein the VEGF trap consists of the amino acid sequence of SEQ ID NO:2.

7. The pre-filled syringe of claim 3 , wherein the VEGF trap consists of the amino acid sequence of SEQ ID NO:4.

8. The pre-filled syringe according to claim 2 wherein the VEGF trap is stable for at least 5 months.

9. The pre-filled syringe according to claim 8 , wherein the VEGF trap consists of amino acids 27-457 of SEQ ID NO:4.

10. The pre-filled syringe according to claim 9 , wherein the stable ophthalmic formulation comprises 40 mg/mL of the VEGF trap, 10 mM phosphate, 135 mM NaCI, and 0.03% polysorbate 20, at pH 6.2-6.4.

11. The pre-filled syringe of claim 8 , wherein the VEGF trap consists of the amino acid sequence of SEQ ID NO:2.

12. The pre-filled syringe of claim 8 , wherein the VEGF trap consists of the amino acid sequence of SEQ ID NO:4.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 14, 2014
From: FURFINE, ERIC; DIX, DANIEL; GRAHAM, KENNETH S.; FRYE, KELLY
To: REGENERON PHARMACEUTICALS, INC.
Reel/Frame 033537/0874 →
Continuity (7)
Continuation 13914996 · Jun 11, 2013
Continuation 13329770 · Dec 19, 2011
Continuation 12833417 · Jul 9, 2010
Continuation 12560885 · Sep 16, 2009
Division 11818463 · Jun 14, 2007
Provisional Application 60814484 · Jun 16, 2006
Related Publication 20140323983A1 · Oct 30, 2014