IP Library Granted Patent US 11,639,397
Granted Patent B2
US 11,639,397 · App. 14/269,950 · Granted May 2, 2023

Bispecific antibodies specific for T-cell activating antigens and a tumor antigen and methods of use

Inventors: Peter Bruenker (Hittnau, CH); Tanja Fauti (Zurich, CH); Christiane Neumann (Wallisellen, CH); Christian Klein (Bonstetten, CH); Pablo Umana (Wollerau, CH)
Assignee: Roche Glycart AG
C07K16/468C07K16/3053C07K16/2809C07K16/30C07K2317/31C07K2317/52C07K2317/55C07K2317/66
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Quick Facts
Patent No.
US 11,639,397
App. No.
14/269,950
Granted
May 2, 2023
Kind
B2
Abstract

The present invention relates to bispecific antibodies that specifically bind a T-cell activating antigen and a Tumor Antigen (TA), comprising a first Fab fragment and a second Fab fragment, wherein either the variable regions or the constant regions of the second Fab heavy and light chain are exchanged; and wherein the bispecific antibody does not comprise a Fc domain; methods for their production, pharmaceutical compositions containing said antibodies, and uses thereof.

Claims (17)

1. A bispecific antibody that specifically binds CD3 and melanoma-associated chondroitin sulfate proteoglycan (MCSP), wherein the bispecific antibody comprises a first Fab fragment, a second Fab fragment, and a peptide linker, wherein either the variable regions or the constant regions of the second Fab heavy and light chain are exchanged, wherein the bispecific antibody does not comprise an Fc domain, wherein the peptide linker connects the C-terminus of the first Fab fragment to the N-terminus of the second Fab fragment or the N terminus of the first Fab fragment to the C-terminus of the second Fab fragment, and wherein the peptide linker comprises the amino acid sequence of SEQ ID NO: 148, (G x S) n , or (G x S) n G m , wherein:

(i) x is 3; n is 3, 4, 5, or 6; and m is 0, 1, 2, or 3; or

(ii) x is 4; n is 2, 3, 4, or 5; and m is 0, 1, 2, or 3.

2. The bispecific antibody of claim 1 , wherein the first fragment comprises at least one antigen binding site specific for MCSP; and the second Fab fragment comprises at least one antigen binding site specific for CD3.

3. The bispecific antibody of claim 1 , additionally comprising a third Fab fragment connected to the first Fab fragment or the second Fab fragment via a second peptide linker comprising the amino acid sequence of SEQ ID NO: 148, (G x S) n , or (G x S) n G m , wherein:

(i) x is 3; n is 3, 4, 5, or 6; and m is 0, 1, 2, or 3; or

(ii) x is 4; n is 2, 3, 4, or 5; and m is 0, 1, 2, or 3.

4. The bispecific antibody of claim 3 , wherein the third Fab fragment comprises at least one antigen binding site specific for MCSP.

5. The bispecific antibody of claim 3 , wherein the third Fab fragment is connected to the first Fab fragment.

6. The bispecific antibody of claim 5 , wherein the C-terminus of the third Fab fragment is connected to the N-terminus of the first Fab fragment.

7. The bispecific antibody of claim 3 , wherein the third Fab fragment is connected to the second Fab fragment.

8. The bispecific antibody of claim 7 , wherein the N-terminus of the third Fab fragment is connected to the C-terminus of the second Fab fragment.

9. The bispecific antibody of claim 1 , wherein the peptide linker is a (G4S) 2 linker.

10. A pharmaceutical composition comprising the bispecific antibody of claim 1 or 3 .

11. A prokaryotic or eukaryotic host cell comprising vectors comprising nucleic acid molecules encoding the light chains and heavy chains of the bispecific antibody of claim 1 or 3 .

12. A method of producing an antibody comprising culturing the host cell of claim 11 so that the antibody is produced.

13. The bispecific antibody of claim 3 , wherein the peptide linker connecting the first Fab fragment to the second Fab fragment is a (G4S) 2 linker and/or the second peptide linker connecting the third Fab fragment to the first Fab fragment or the second Fab fragment is a (G4S) 2 linker.

Priority Claims (1)
EP 1178410 · Aug 23, 2011 · regional
Continuity (2)
Continuation 13591024 · Aug 21, 2012
Related Publication 20150274845A1 · Oct 1, 2015