The patent badge is an abbreviated version of the USPTO patent document. The patent badge does contain a link to the full patent document.

The patent badge is an abbreviated version of the USPTO patent document. The patent badge covers the following: Patent number, Date patent was issued, Date patent was filed, Title of the patent, Applicant, Inventor, Assignee, Attorney firm, Primary examiner, Assistant examiner, CPCs, and Abstract. The patent badge does contain a link to the full patent document (in Adobe Acrobat format, aka pdf). To download or print any patent click here.

Date of Patent:
Sep. 26, 2023

Filed:

Jun. 20, 2019
Applicant:

Hoffmann-la Roche Inc., Little Falls, NJ (US);

Inventors:

Thomas Dams, Penzberg, DE;

Roberto Falkenstein, Penzberg, DE;

Sebastian Malik, Penzberg, DE;

Ingrid Grunert, Penzberg, DE;

Marco Thomann, Penzberg, DE;

Matthias Freiherr Von Roman, Penzberg, DE;

Heiko Walch, Penzberg, DE;

Assignee:

Hoffmann-La Roche Inc., Little Falls, NJ (US);

Attorney:
Primary Examiner:
Int. Cl.
CPC ...
C07K 1/18 (2006.01); C07K 16/18 (2006.01); C12N 9/10 (2006.01); C12P 21/00 (2006.01); A61K 45/06 (2006.01);
U.S. Cl.
CPC ...
C07K 1/18 (2013.01); C07K 16/18 (2013.01); C12N 9/1051 (2013.01); C12N 9/1081 (2013.01); C12P 21/005 (2013.01); A61K 45/06 (2013.01); C12Y 204/01038 (2013.01); C12Y 204/99003 (2013.01);
Abstract

Herein is reported a method for the enzymatic production of an antibody with a modified glycosylation in the Fc-region comprising the steps of incubating the antibody light chain affinity ligand-bound monoclonal antibody with a glycosylation in the Fc-region with a first enzyme for a time sufficient and under conditions suitable to modify the glycosylation of the Fc-region, recovering the antibody from the antibody light chain affinity ligand, incubating the recovered antibody in solution with a second enzyme for a time sufficient and under conditions suitable to modify the glycosylation of the Fc-region to a defined form, separating the antibody with the modified glycosylation in the Fc-region from the second enzyme in a cation exchange chromatography, and thereby producing the antibody with a modified glycosylation in the Fc-region.


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