IP Library Granted Patent US 8,802,107
Granted Patent B2
US 8,802,107 · App. 13/914,996 · Granted Aug 12, 2014

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
C07K14/4705C07K2319/30A61K38/1793A61K9/19A61K9/0048
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Quick Facts
Patent No.
US 8,802,107
App. No.
13/914,996
Granted
Aug 12, 2014
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 (26)

1. A method of producing a lyophilized formulation of a VEGF antagonist, comprising a step of subjecting to lyophilization a pre-lyophilized formulation, which comprises:

(a) 5-50 mg/ml of a vascular endothelial growth factor (VEGF) antagonist, comprising the amino acids 27-457 of SEQ ID NO:4;

(b) 5-25 mM of sodium phosphate buffer, pH about 5.8-7.0;

(c) 0.01-0.15% of an organic co-solvent, selected from the group consisting of polysorbate, polythylene glycol (PEG) propylene glycol, and a combination thereof; and,

(d) 1-10% of a stabilizing agent selected from the group consisting of sucrose, sorbitol, glycerol, trehalose, and mannitol, to generate a lyophilized formulation.

2. The method of claim 1 , wherein the prelyophilization formulation comprises about 20 mg/ml of the VEGF antagonist, about 10 mM sodium phosphate buffer, about 0.03% polysorbate, about 0.1% PEG, and about 2.5% sucrose, pH about 6.2-6.3.

3. The method of claim 1 , wherein the prelyophilization formulation comprises about 20 mg/ml of the VEGF antagonist, about 5 mM sodium phosphate buffer, about 0.015% polysorbate, about 2.5% sucrose, and further comprising sodium chloride at about 20 mM, pH about 6.2-6.3.

4. The method of claim 1 , wherein the prelyophilization formulation comprises about 20 mg/ml of the VEGF antagonist, about 5 mM sodium phosphate buffer, about 0.015% polysorbate, and further comprising sodium chloride at about 67.5 mM, pH about 6.2-6.3.

5. A lyophilized formulation made according to the method of claim 1 .

6. The lyophilized formulation of claim 5 , wherein the prelyophilization formulation comprises about 20 mg/ml of the VEGF antagonist, about 10 mM sodium phosphate buffer, about 0.03% polysorbate, about 0.1% PEG, and about 2.5% sucrose, pH about 6.2-6.3.

7. The lyophilized formulation of claim 5 , wherein the prelyophilization formulation comprises about 20 mg/ml of the VEGF antagonist, about 5 mM sodium phosphate buffer, about 0.015% polysorbate, about 2.5% sucrose, and further comprising sodium chloride at about 20 mM, pH about 6.2-6.3.

8. The lyophilized formulation of claim 5 , wherein the prelyophilization formulation comprises about 20 mg/ml of the VEGF antagonist, about 5 mM sodium phosphate buffer, about 0.015% polysorbate, and further comprising sodium chloride at about 67.5 mM, pH about 6.2-6.3.

9. A method of producing a lyophilized formulation of a VEGF antagonist, comprising the step of subjecting to lyophilization a prelyophilization formulation, which comprises

a) 5-50 mg/ml of a vascular endothelial growth factor (VEGF) antagonist, comprising amino acids 27-457 of SEQ ID NO:4;

(b) 5-25 mM of a phosphate buffer, pH about 5.8-7.0;

(c) 0.01-0.15% of an organic co-solvent, selected from the group consisting of polysorbate, polyethylene glycol (PEG), propylene glycol, and a combination thereof; and

(d) 20-150 mM of a tonicity agent, to generate a lyophilized formulation.

10. The method of claim 9 , wherein the tonicity agent is sodium chloride at a concentration selected from the group consisting of 20 mM and 67.5 mM.

11. The method of claim 9 , wherein the organic co-solvent is polysorbate at 0.015%.

12. The method of claim 9 , wherein the VEGF antagonist is at a concentration selected from the group consisting of 5 mg/ml, 10 mg/ml, 20 mg/ml, and 40 mg/ml.

13. The method of claim 9 , wherein the sodium phosphate buffer is at 5 mM.

14. A lyophilized formulation made according to the method of claim 9 .

15. The lyophilized formulation of claim 14 , wherein the tonicity agent is sodium chloride at a concentration selected from the group consisting of 20 mM and 67.5 mM.

16. The lyophilized formulation of claim 14 , wherein the organic co-solvent is polysorbate at 0.015%.

17. The lyophilized formulation of claim 14 , wherein the VEGF antagonist is at a concentration selected from the group consisting of 5 mg/ml, 10 mg/ml, 20 mg/ml, and 40 mg/ml.

18. The lyophilized formulation of claim 14 , wherein the sodium phosphate buffer is at 5 mM.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 7, 2014
From: FURFINE, ERIC; DIX, DANIEL B; GRAHAM, KENNETH S; FRYE, KELLY
To: REGENERON PHARMACEUTICALS, INC.
Reel/Frame 032616/0301 →
Continuity (6)
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 20130274189A1 · Oct 17, 2013