IP Library Granted Patent US 8,916,153
Granted Patent B2
US 8,916,153 · App. 13/927,236 · Granted Dec 23, 2014

Purified antibody composition

Inventors: Min M. Wan (Worcester, MA); George Avgerinos (Sudbury, MA); Gregory Zarbis-Papastoitsis (Watertown, MA)
Assignee: AbbVie Biotechnology Ltd.
A61K39/3955C07K1/18C07K1/36C07K16/065C07K16/241
View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 8,916,153
App. No.
13/927,236
Granted
Dec 23, 2014
Kind
B2
Abstract

The invention provides a method for producing a host cell protein-(HCP) reduced antibody preparation from a mixture comprising an antibody and at least one HCP, comprising an ion exchange separation step wherein the mixture is subjected to a first ion exchange material, such that the HCP-reduced antibody preparation is obtained.

Claims (18)

1. A pharmaceutical composition comprising adalimumab and a pharmaceutically acceptable carrier, wherein the adalimumab is produced in a Chinese Hamster Ovary (CHO) cell expression system; and wherein the composition is characterized in that when the composition is assayed in a cathepsin L kinetic assay, a level of cathepsin L activity from 0.4 to less than 1.84 RFU/s/mg of adalimumab is observed, wherein the cathepsin L kinetic assay comprises:

i) diluting the composition in a polystyrene container in a solution containing 25 mM NaOAc, 5 mM DTT and 1 mM EDTA at pH 5.5,

ii) adding dextran sulfate to a concentration of 0.035 μg/mL and incubating at 37° C. for six hours,

iii) adding Z-leucine-arginine covalently bound at its C-terminus to a fluorescent 7-amino-4-methyl coumarin (Z-leucine-arginine-AMC), wherein the diluting, adding, and incubating steps are sufficient to permit the measurement of cathepsin L hydrolysis of the Z-leucine-arginine-AMC within a linear range, and

iv) measuring Z-leucine-arginine-AMC hydrolysis in the linear range in RFU/s/mg of adalimumab.

2. The pharmaceutical composition of claim 1 , wherein the cathepsin L activity is from 0.4 to 1.3 RFU/s/mg of adalimumab.

3. The pharmaceutical composition of claim 1 , wherein the cathepsin L activity is from 0.5 to 1.5 RFU/s/mg of adalimumab.

4. The pharmaceutical composition of claim 1 , wherein the cathepsin L activity is from 0.4 to 1.0 RFU/s/mg of adalimumab.

5. The pharmaceutical composition of claim 1 , wherein the cathepsin L activity is from 0.4 to 0.6 RFU/s/mg of adalimumab.

6. The pharmaceutical composition of claim 1 , wherein the cathepsin L activity is from 0.4 to 0.85 RFU/s/mg of adalimumab.

7. The pharmaceutical composition of claim 1 , wherein the cathepsin L activity is from 0.4 to 0.9 RFU/s/mg of adalimumab.

8. The pharmaceutical composition of any one of claims 1 - 3 and 4 - 7 , wherein the composition is packaged in a pre-filled syringe.

9. The pharmaceutical composition of any one of claims 1 - 3 and 4 - 7 , wherein the composition comprises 50 mg/ml of adalimumab.

10. The pharmaceutical composition of any one of claims 1 - 3 and 4 - 7 , wherein the composition further comprises mannitol.

11. The pharmaceutical composition of any one of claims 1 - 3 and 4 - 7 , wherein the composition is suitable for subcutaneous injection.

12. The pharmaceutical composition of any one of 1 - 3 and 4 - 7 , wherein step i) of the cathepsin L kinetic assay comprises diluting the composition 600 fold.

13. The pharmaceutical composition of any one of claims 1 - 3 and 4 - 7 , wherein the diluted composition has an adalimumab concentration of 50 μg/ml.

14. The pharmaceutical composition of any one of claims 1 - 3 and 4 - 7 , wherein the diluted composition has an adalimumab concentration of 20 μg/ml.

Assignments (1)
CHANGE OF NAME Recorded Sep 13, 2013
From: ABBOTT BIOTECHNOLOGY LTD.
To: ABBVIE BIOTECHNOLOGY LTD.
Reel/Frame 031217/0161 →
Continuity (6)
Continuation 13532511 · Jun 25, 2012
Continuation 12882601 · Sep 15, 2010
Division 11732918 · Apr 4, 2007
Provisional Application 60789725 · Apr 5, 2006
Provisional Application 60790414 · Apr 6, 2006
Related Publication 20130273059A1 · Oct 17, 2013