IP Library Granted Patent US 11,773,166
Granted Patent B2
US 11,773,166 · App. 16/159,231 · Granted Oct 3, 2023

CD3/CD38 T cell retargeting hetero-dimeric immunoglobulins and methods of their production

Inventors: Romain Ollier (La Chaux-de-Fonds, CH); Samuel Hou (La Chaux-de-Fonds, CH); Rami Lissilaa (La Chaux-de-Fonds, CH); Darko Skegro (La Chaux-de-Fonds, CH); Jonathan Back (La Chaux-de-Fonds, CH)
Assignee: Ichnos Sciences SA
C07K16/2809A61P35/00C07K16/2896A61K38/00C07K2317/24C07K2317/31C07K2317/33C07K2317/52C07K2317/524C07K2317/55C07K2317/565C07K2317/622C07K2317/73C07K2317/94
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Quick Facts
Patent No.
US 11,773,166
App. No.
16/159,231
Granted
Oct 3, 2023
Kind
B2
Abstract

The present invention relates to hetero-dimeric immunoglobulins that target both a component of the human CD3 antigen and a component of the human CD38 antigen and methods of making the same. The present invention also relates to antibodies which bind to the human CD38 antigen and derivatives thereof for use as therapeutic or diagnostic reagents and methods of making the same.

Claims (12)

1. A bispecific antibody or fragment thereof that binds to human CD38 comprising a heavy chain variable region CDR1 comprising the amino acid sequence of SEQ ID NO: 25 or SEQ ID NO: 208, a heavy chain variable region CDR2 comprising the amino acid sequence of SEQ ID NO: 26 or SEQ ID NO: 209, and a heavy chain variable region CDR3 comprising the amino acid sequence of SEQ ID NO: 27 or SEQ ID NO: 210; and comprising a light chain variable region CDR1 comprising the amino acid sequence of SEQ ID NO: 28 or SEQ ID NO: 211 or SEQ ID NO: 214, a light chain variable region CDR2 comprising the amino acid sequence of SEQ ID NO: 29 or SEQ ID NO: 212, and a light chain variable region CDR3 comprising the amino acid sequence of SEQ ID NO: 30 or SEQ ID NO: 213.

2. The bispecific antibody or fragment thereof of claim 1 , wherein the bispecific antibody or fragment thereof is a murine antibody, chimeric antibody or a humanized antibody.

3. The bispecific antibody or fragment thereof of claim 1 , wherein the bispecific antibody or fragment thereof comprises a heavy chain variable region sequence comprising the amino acid sequence selected from the group consisting of SEQ ID NO: 52, SEQ ID NO: 58, and SEQ ID NO: 60 or a sequence at least 80% identical to the non-CDR region of said heavy chain variable region sequences and/or wherein the bispecific antibody or fragment thereof comprises a light chain variable region sequence comprising the amino acid sequence selected from the group consisting of SEQ ID NO: 55, SEQ ID NO: 59, and SEQ ID NO: 61 or a sequence at least 80% identical to the non-CDR region of any one of said light chain variable region sequences.

4. The bispecific antibody or fragment thereof of claim 1 , wherein the bispecific antibody or fragment thereof comprises a heavy chain sequence comprising the amino acid sequence selected from the group consisting of SEQ ID NO: 73, SEQ ID NO: 75, SEQ ID NO: 76, SEQ ID NO: 145, SEQ ID NO: 147, and SEQ ID NO: 149 or a sequence at least 80% identical to the non-CDR region of said heavy chain variable region sequences and/or wherein the bispecific antibody or fragment thereof comprises a light chain region sequence comprising the amino acid sequence selected from the group consisting of SEQ ID NO: 74, SEQ ID NO: 77, SEQ ID NO: 146, SEQ ID NO: 148, and SEQ ID NO: 150 or a sequence at least 80% identical to the non-CDR region of any one of said light chain variable region sequences.

5. The bispecific antibody or fragment thereof of claim 1 , wherein said bispecific antibody or fragment comprises human heavy and/or light chain constant regions and wherein the human heavy constant region is selected from the group of human immunoglobulins consisting of IGHG1, non fucosylated IGHG1 and IGHG4.

6. The bispecific antibody or fragment thereof of claim 1 , wherein said bispecific antibody fragment is selected from the group consisting of Fab, Fab′, Fab′-SH, Fd, Fv, dAb, F(ab′)2, scFv, bispecific single chain Fv dimers, diabodies, triabodies and scFv.

7. The bispecific antibody or fragment thereof of claim 1 , further comprising an anti-CD3 antibody fragment selected from the group consisting of Fab, Fab′, Fab′-SH, Fd, Fv, dAb, F(ab′)2, scFv, bispecific single chain Fv dimers, diabodies, triabodies and scFv.

8. The bispecific antibody or fragment thereof of claim 7 , wherein said anti-CD3 antibody fragment comprises a heavy chain variable region CDR1 comprising the amino acid sequence of SEQ ID NO: 3, a heavy chain variable region CDR2 comprising the amino acid sequence of SEQ ID NO: 4, and a heavy chain variable region CDR3 comprising the amino acid sequence of SEQ ID NO: 5 or SEQ ID NO: 9; and comprises a light chain variable region CDR1 comprising the amino acid sequence of SEQ ID NO: 6, a light chain variable region CDR2 comprising the amino acid sequence of SEQ ID NO: 7 or SEQ ID NO: 11, and a light chain variable region CDR3 comprising the amino acid sequence of SEQ ID NO: 8, SEQ ID NO: 10, or SEQ ID NO: 12; or wherein said anti-CD3 antibody fragment comprises a heavy chain variable region CDR1 comprising the amino acid sequence of SEQ ID NO: 163, a heavy chain variable region CDR2 comprising the amino acid sequence of SEQ ID NO: 164, and a heavy chain variable region CDR3 comprising the amino acid sequence of SEQ ID NO: 165; and comprises a light chain variable region CDR1 comprising the amino acid sequence of SEQ ID NO: 166, a light chain variable region CDR2 comprising the amino acid sequence of SEQ ID NO: 167, and a light chain variable region CDR3 comprising the amino acid sequence of SEQ ID NO: 168.

9. A composition comprising the bispecific antibody or fragment thereof of claim 1 and a pharmaceutically acceptable carrier.

10. An immunoconjugate comprising the bispecific antibody or fragment thereof of claim 1 , linked to a therapeutic agent.

11. A method of treating a disease selected from the group consisting of malignant hematological diseases, including multiple myeloma, B-cell chronic lymphocytic leukaemia, B-cell acute lymphocytic leukaemia, Waldenstrom's macroglobulinemia, primary systemic amyloidosis, mantle-cell lymphoma, pro-lymphocytic/myelocytic leukaemia, acute myeloid leukaemia, chronic myeloid leukaemia, follicular lymphoma, NK-cell leukaemia, and plasma-cell leukaemia comprising administering the bispecific antibody or fragment thereof of claim 1 to a subject in need thereof.

12. The bispecific antibody or fragment thereof of claim 7 , wherein said anti-CD3 antibody fragment comprises the amino acid sequence of SEQ ID NO: 67, 68, 69, or 70.

Assignments (3)
CHANGE OF NAME Recorded Aug 25, 2025
From: ICHNOS SCIENCES SA
To: IGI THERAPEUTICS SA
Reel/Frame 072111/0007 →
CHANGE OF NAME Recorded Jan 31, 2020
From: GLENMARK PHARMACEUTICALS S.A.
To: ICHNOS SCIENCES SA
Reel/Frame 052159/0045 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 14, 2019
From: OLLIER, ROMAIN; HOU, SAMUEL; LISSILAA, RAMI; SKEGRO, DARKO; BACK, JONATHAN
To: GLENMARK PHARMACEUTICALS S.A.
Reel/Frame 047988/0925 →
Priority Claims (1)
EP 15167034 · May 8, 2015 · regional
Continuity (2)
Continuation 15524485
Related Publication 20190135918A1 · May 9, 2019
Cited By (1)
US 12,433,953