IP Library › Granted Patent US 10,640,555
Granted Patent B2
US 10,640,555 · App. 15/495,641 · Granted May 5, 2020

Bispecific antigen binding proteins

Inventors: Sabine Imhof-Jung (Planegg, DE); Christian Klein (Bonstetten, CH); Joerg Thomas Regula (Munich, DE); Wolfgang Schaefer (Mannheim, DE); Juergen Michael Schanzer (Traunstein, DE)
Assignee: HOFFMANN-LA ROCHE INC.
C07K16/22C07K16/468C07K2317/31C07K2317/35C07K2317/55C07K2317/56C07K2317/64C07K2317/66C07K2317/73C07K2317/76C07K2319/00
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 10,640,555
App. No.
15/495,641
Granted
May 5, 2020
Kind
B2
Abstract

The present invention relates to bispecific antigen binding proteins, methods for their production, pharmaceutical compositions containing said antibodies, and uses thereof.

Claims (37)

1. A method for the preparation of a bispecific antigen binding protein comprising:

a) two light chains and two heavy chains of an antibody that comprises two Fab fragments and that specifically binds to a first antigen; and

b) two additional Fab fragments of an antibody which specifically binds to a second antigen, wherein the additional Fab fragments are both fused via a peptide connector either at the C- or N-termini of the heavy chains of a);

wherein the bispecific antigen binding protein also comprises a structural modification selected from the group consisting of:

i) in both Fab fragments of a) or in both Fab fragments of b) the variable domains VL and VH are replaced by each other, and the constant domains CL and CH1 are replaced by each other, or the constant domains CL and CH1 are replaced by each other;

ii) in both Fab fragments of a)

the variable domains VL and VH are replaced by each other,

and

the constant domains CL and CH1 are replaced by each other, and in both Fab fragments of b)

the variable domains VL and VH are replaced by each other,

or

the constant domains CL and CH1 are replaced by each other;

iii) in both Fab fragments of a)

the variable domains VL and VH are replaced by each other,

or

the constant domains CL and CH1 are replaced by each other,

and

in both Fab fragments of b)

the variable domains VL and VH are replaced by each other,

and

the constant domains CL and CH1 are replaced by each other;

iv) in both Fab fragments of a)

the variable domains VL and VH are replaced by each other,

and

in both Fab fragments of b)

the constant domains CL and CH1 are replaced by each other;

and

v) in both Fab fragments of a)

the constant domains CL and CH1 are replaced by each other,

and

in both Fab fragments of b)

the variable domains VL and VH are replaced by each other,

comprising the steps of

a) transforming a host cell with vectors comprising nucleic acid molecules encoding said bispecific antigen binding protein;

b) culturing the host cell under conditions that allow synthesis of said antigen binding protein molecule; and

c) recovering said antigen binding protein molecule from said culture.

2. A host cell comprising the vectors according to claim 1 .

Priority Claims (1)
EP 09007857 · Jun 16, 2009 · regional
Continuity (2)
Division 12780971 · May 17, 2010
Related Publication 20180079805A1 · Mar 22, 2018