IP Library Granted Patent US 10,323,099
Granted Patent B2
US 10,323,099 · App. 15/092,847 · Granted Jun 18, 2019

Multispecific domain exchanged common variable light chain antibodies

Inventors: Peter Bruenker (Hittnau, CH); Christiane Neumann (Niederweningen, CH); Christian Klein (Bonstetten, CH); Ekkehard Moessner (Kreuzlingen, CH); Wolfgang Schaefer (Mannheim, DE)
Assignee: Hoffmann-La Roche Inc.
C07K16/40C07K16/2878C07K16/3053C07K2317/24C07K2317/31C07K2317/35C07K2317/41C07K2317/51C07K2317/515C07K2317/522C07K2317/524C07K2317/526C07K2317/56C07K2317/60C07K2317/73
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Quick Facts
Patent No.
US 10,323,099
App. No.
15/092,847
Granted
Jun 18, 2019
Kind
B2
Abstract

Multispecific antibodies based on antibodies that share a common light chain are described herein. The multispecific antibodies include: modified heavy chains having, by domain exchange, a common light chain variable domain VL; and two modified light chains having, by domain exchange, variable heavy chain domains of a first antibody (VH 1 ) and a second antibody (VH 2 ), wherein one light chain is of kappa isotype and one light chain is of lambda isotype. The present invention also relates to methods for the manufacture of such antibodies and their use.

Claims (29)

1. A multispecific antibody, comprising:

(a) a first modified light chain, wherein the first modified light chain comprises in C-terminal to N-terminal direction:

a constant light chain domain of kappa isotype (CLκ); and

a variable heavy chain domain (VH 1 ) derived from an antibody which specifically binds to a first antigen;

(b) a second modified light chain, wherein the second modified light chain comprises in C-terminal to N-terminal direction:

a constant light chain domain of lambda isotype (CLλ); and

a variable heavy chain domain (VH 2 ) derived from an antibody which specifically binds to a second antigen; and

(c) two modified heavy chains, wherein each modified heavy chain comprises in C-terminal to N-terminal direction:

heavy chain constant domains 3 and 2 (CH3 and CH2);

a hinge region;

a heavy chain constant domain 1 (CH1); and

a light chain variable domain (VL),

wherein the VL in one of the two modified heavy chains and the VL in the other of the two modified heavy chains are identical,

wherein the first modified light chain of (a) pairs with one of the two modified heavy chains to form a first antigen binding site which specifically binds to the first antigen, and

wherein the second modified light chain of (b) pairs with the other of the two modified heavy chains to form a second antigen binding site which specifically binds to the second antigen.

2. The multispecific antibody according to claim 1 , wherein the antibody is a bivalent, bispecific antibody.

3. The multispecific antibody according to claim 1 , wherein the antibody is of IgG class.

4. The multispecific antibody according to claim 1 , wherein the antibody is of IgG1 or IgG4 subclass.

5. A pharmaceutical composition comprising the multispecific antibody according to claim 1 and at least one pharmaceutically acceptable excipient.

6. A pharmaceutical composition comprising the multispecific antibody according to claim 2 and at least one pharmaceutically acceptable excipient.

7. A pharmaceutical composition comprising the multispecific antibody according to claim 3 and at least one pharmaceutically acceptable excipient.

8. A pharmaceutical composition comprising the multispecific antibody according to claim 4 and at least one pharmaceutically acceptable excipient.

9. A nucleic acid encoding a multispecific antibody according to claim 1 .

10. An expression vector containing a nucleic acid that encodes the multispecific antibody of claim 1 .

11. A prokaryotic or eukaryotic host cell comprising an expression vector according to claim 10 .

12. A method for the preparation of a multispecific antibody according to claim 1 , comprising the steps of

a) transforming a host cell with expression vectors comprising nucleic acid molecules encoding a multispecific antibody according to claim 1 ;

b) culturing the host cell under conditions that allow synthesis of said multispecific antibody molecule; and

c) recovering said multispecific antibody molecule from said culture.

Assignments (5)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 21, 2016
From: BRUENKER, PETER; JAEGER, CHRISTIANE; KLEIN, CHRISTIAN; MOESNER, EKKEHARD
To: ROCHE GLYCART AG
Reel/Frame 039216/0062 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 21, 2016
From: ROCHE DIAGNOSTICS GMBH
To: F. HOFFMANN-LA ROCHE AG
Reel/Frame 039216/0108 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 21, 2016
From: ROCHE GLYCART AG
To: F. HOFFMANN-LA ROCHE AG
Reel/Frame 039216/0162 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 21, 2016
From: SCHAEFER, WOLFGANG
To: ROCHE DIAGNOSTICS GMBH
Reel/Frame 039216/0186 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 21, 2016
From: F. HOFFMANN-LA ROCHE AG
To: HOFFMANN-LA ROCHE INC.
Reel/Frame 039216/0218 →
Priority Claims (1)
EP 13188283 · Oct 11, 2013 · regional
Continuity (2)
Continuation PCTEP2014071531 · Oct 8, 2014
Related Publication 20160319036A1 · Nov 3, 2016
Cited By (5)
US 12,252,533 US 12,358,997 US 12,509,527 US 12,540,194 US 12,735,497