IP Library Granted Patent US 9,676,845
Granted Patent B2
US 9,676,845 · App. 12/780,971 · Granted Jun 13, 2017

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 9,676,845
App. No.
12/780,971
Granted
Jun 13, 2017
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 (41)

1. 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.

2. The bispecific antigen binding protein according to claim 1

wherein said additional Fab fragments are both fused via a peptide connector either to the C-termini of the heavy chains of a), or to the N-termini of the heavy chains of a).

3. The bispecific antigen binding protein according to claim 1 , wherein the Fab fragments comprise the following structural modifications:

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.

4. The bispecific antigen binding protein according to claim 3 , wherein the Fab fragments comprise the following structural modifications:

i) 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, or the constant domains CL and CH1 are replaced by each other.

5. The bispecific antigen binding protein according to claim 4 , wherein the Fab fragments comprise the following structural modifications:

i) in both Fab fragments of a)

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

6. The bispecific antigen binding protein according to claim 3 , wherein the Fab fragments comprise the following structural modifications:

i) 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.

7. The bispecific antigen binding protein according to claim 6 , the Fab fragments comprise the following structural modifications:

i) in both Fab fragments of b)

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

8. A pharmaceutical composition comprising the bispecific antigen binding protein according to claim 1 and at least one pharmaceutically acceptable excipient.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 30, 2010
From: F. HOFFMANN-LA ROCHE AG
To: HOFFMANN-LA ROCHE, INC.
Reel/Frame 024910/0105 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 30, 2010
From: IMHOF-JUNG, SABINE; KLEIN, CHRISTIAN; REGULA, JOERG THOMAS; SCHAEFER, WOLFGANG; SCHANZER, JUERGEN MICHAEL
To: F. HOFFMANN-LA ROCHE AG
Reel/Frame 024918/0986 →
Priority Claims (1)
EP 09007857 · Jun 16, 2009 · regional
Continuity (1)
Related Publication 20100316645A1 · Dec 16, 2010