IP Library Granted Patent US 10,358,492
Granted Patent B2
US 10,358,492 · App. 14/040,023 · Granted Jul 23, 2019

Bispecific IgG antibodies as T cell engagers

Inventors: Alexander Berthold Hendrik Bakker (Utrecht, NL); Pieter Fokko Van Loo (Utrecht, NL); Ton Logtenberg (Utrecht, NL)
Assignee: Merus N.V.
C07K16/28C07K16/2809C07K16/2851C07K16/3061A61K2039/505C07K2317/21C07K2317/31C07K2317/526C07K2317/53C07K2317/55C07K2317/569C07K2317/70C07K2317/71C07K2317/73C07K2317/92
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 10,358,492
App. No.
14/040,023
Granted
Jul 23, 2019
Kind
B2
Abstract

Bispecific IgG antibodies which bind to CLEC12A and an antigen on an immune effector cell are provided.

Claims (48)

1. A bispecific IgG antibody comprising

a first arm that specifically recognizes CLEC12A, wherein said first arm comprises a heavy chain CDR1 comprising the amino acid sequence SGYTFTGY (SEQ ID NO: 1), a heavy chain CDR2 comprising the amino acid sequence IINPSGGS (SEQ ID NO: 2), and a heavy chain CDR3 comprising the amino acid sequence GTTGDWFDY (SEQ ID NO: 3); and

a second arm that specifically recognizes an antigen on immune effector cells capable of recruiting such cells to an aberrant cell expressing CLEC12A.

2. The bispecific IgG antibody according to claim 1 , wherein the arm that specifically recognizes CLEC12A comprises a variable heavy chain that is at least 90% identical to the amino acid sequence:

QVQLVQSGAEVKKPGASVKVSCKASGYTFTSYYMHWVRQAPGQGLEWMGIINPS GGSTSYAQKFQGRVTMTRDTSTSTVYMELSSLRSEDTAVYYCAKGTTGDWFDYW GQGTLVTVSS (SEQ ID NO: 4).

3. The bispecific antibody according to claim 1 , wherein said first arm that specifically recognizes CLEC12A comprises a variable heavy chain comprising the amino acid sequence:

QVQLVQSGAEVKKPGASVKVSCKASGYTFTSYYMHWVRQAPGQGLEWMGIINPS GGSTSYAQKFQGRVTMTRDTSTSTVYMELSSLRSEDTAVYYCAKGTTGDWFDYW GQGTLVTVSS (SEQ ID NO: 4).

4. The bispecific IgG antibody according to claim 1 , wherein the variable light chain of said first arm comprises a variable light chain CDR1 comprising the amino acid sequence RASQSISSYLN (SEQ ID NO: 17), a light chain CDR2 comprising the amino acid sequence AASSLQS (SEQ ID NO: 18), and a light chain CDR3 comprising the amino acid sequence QQSYSTPPT (SEQ ID NO: 19).

5. The bispecific IgG antibody according to claim 4 , wherein the first arm comprises a variable light chain that is at least 90% identical to the amino acid sequence:

DIQMTQSPSSLSASVGDRVTITCRASQSISSYLNWYQQKPGKAPKLLIYAASSLQSGV PSRFSGSGSGTDFTLTISSLQPEDFATYYCQQSYSTPPTFGQGTKVEIK (SEQ ID NO: 20).

6. The bispecific IgG antibody according to claim 5 , wherein the first arm comprises a variable light chain comprising the amino acid sequence:

DIQMTQSPSSLSASVGDRVTITCRASQSISSYLNWYQQKPGKAPKLLIYAASSLQSGV PSRFSGSGSGTDFTLTISSLQPEDFATYYCQQSYSTPPTFGQGTKVEIK (SEQ ID NO: 20).

7. The bispecific IgG antibody according to claim 1 , wherein said first and second arms comprise a common light chain.

8. The bispecific IgG antibody according to claim 1 , comprising a mutated CH2 and/or lower hinge domains wherein the binding of said bispecific antibody with Fcγ receptors is significantly reduced.

9. The bispecific IgG antibody according to claim 8 , wherein said mutated CH2 and/or lower hinge domains comprise amino acid substitution L235G and/or G236R.

10. The bispecific IgG according to claim 1 , wherein said second arm specifically recognizes CD3.

11. A bispecific IgG antibody comprising

a first arm comprising a V H and a V L , wherein said first arm specifically recognizes CLEC12A and comprises a heavy chain CDR1 comprising the amino acid sequence SGYTFTSY (SEQ ID NO: 5), a heavy chain CDR2 comprising the amino acid sequence IINPSGGS (SEQ ID NO: 6), and a heavy chain CDR3 comprising the amino acid sequence GNYGDEFDY (SEQ ID NO: 7); and

a second arm comprising a V H and a V L , wherein said second arm specifically recognizes an antigen on immune effector cells capable of recruiting such cells to an aberrant cell expressing CLEC12A.

12. The bispecific IgG antibody according to claim 11 , wherein the arm that specifically recognizes CLEC12A comprises a variable heavy chain that is at least 90% identical to the amino acid sequence:

EVQLVQSGAEVKKPGASVKVSCKASGYTFTSYYMHWVRQAPGQGLEWMGIINPSG GSTSYAQKFQGRVTMTRDTSTSTVYMELSSLRSEDTAVYYCARGNYGDEFDYWGQ GTLVTVSS (SEQ ID NO: 8).

13. The bispecific antibody according to claim 11 , wherein said first arm that specifically recognizes CLEC12A comprises a variable heavy chain comprising the amino acid sequence:

EVQLVQSGAEVKKPGASVKVSCKASGYTFTSYYMHWVRQAPGQGLEWMGIINPSG GSTSYAQKFQGRVTMTRDTSTSTVYMELSSLRSEDTAVYYCARGNYGDEFDYWGQ GTLVTVSS (SEQ ID NO: 8).

14. The bispecific IgG antibody according to claim 11 , wherein the variable light chain of said first arm comprises a variable light chain CDR1 comprising the amino acid sequence RASQSISSYLN (SEQ ID NO: 17), a light chain CDR2 comprising the amino acid sequence AASSLQS (SEQ ID NO: 18), and a light chain CDR3 comprising the amino acid sequence QQSYSTPPT (SEQ ID NO: 19).

15. The bispecific IgG antibody according to claim 14 , wherein the first arm comprises a variable light chain that is at least 90% identical to the amino acid sequence:

DIQMTQSPSSLSASVGDRVTITCRASQSISSYLNWYQQKPGKAPKLLIYAASSLQSGV PSRFSGSGSGTDFTLTISSLQPEDFATYYCQQSYSTPPTFGQGTKVEIK (SEQ ID NO: 20).

16. The bispecific IgG antibody according to claim 15 , wherein the first arm comprises a variable light chain comprising the amino acid sequence:

DIQMTQSPSSLSASVGDRVTITCRASQSISSYLNWYQQKPGKAPKLLIYAASSLQSGV PSRFSGSGSGTDFTLTISSLQPEDFATYYCQQSYSTPPTFGQGTKVEIK (SEQ ID NO: 20).

17. The bispecific IgG antibody according to claim 11 , wherein said first and second arms comprise a common light chain.

18. The bispecific IgG antibody according to claim 11 , comprising a mutated CH2 and/or lower hinge domains wherein the binding of said bispecific antibody with Fcγ receptors is significantly reduced.

19. The bispecific IgG antibody according to claim 18 , wherein said mutated CH2 and/or lower hinge domains comprise amino acid substitution L235G and/or G236R.

20. The bispecific IgG according to claim 11 , wherein said second arm specifically recognizes CD3.

21. A bispecific IgG antibody comprising

a first arm comprising a V H and a V L , wherein said first arm specifically recognizes CLEC12A, and a heavy chain CDR1 comprising the amino acid sequence SGYTFTGY (SEQ ID NO: 9), a heavy chain CDR2 comprising the amino acid sequence WINPNSGG (SEQ ID NO: 10), and a heavy chain CDR3 comprising the amino acid sequence DGYFADAFDY (SEQ ID NO: 11); and

a second arm comprising a V H and a V L , wherein said second arm specifically recognizes an antigen on immune effector cells capable of recruiting such cells to an aberrant cell expressing CLEC12A.

22. The bispecific IgG antibody according to claim 21 , wherein the arm that specifically recognizes CLEC12A comprises a variable heavy chain that is at least 90% identical to the amino acid sequence:

QVQLVQSGAEVKKPGASVKVSCKASGYTFTSYYMHWVRQAPGQGLEWMGIINPS GGSTSYAQKFQGRVTMTRDTSTSTVYMELSSLRSEDTAVYYCAKGTTGDWFDYW GQGTLVTVSS (SEQ ID NO: 4).

23. The bispecific antibody according to claim 21 , wherein said first arm that specifically recognizes CLEC12A comprises a variable heavy chain comprising the amino acid sequence:

QVQLVQSGAEVKKPGASVKVSCKASGYTFTGYYMHWVRQAPGQGLEWMGWINP NSGGTNYAQKFQGRVTMTRDTSISTAYMELSRLRSDDTAVYYCARDGYFADAFDY WGQGTLVTVSS (SEQ ID NO: 12).

24. The bispecific IgG antibody according to claim 21 , wherein the variable light chain of said first arm comprises a variable light chain CDR1 comprising the amino acid sequence RASQSISSYLN (SEQ ID NO: 17), a light chain CDR2 comprising the amino acid sequence AASSLQS (SEQ ID NO: 18), and a light chain CDR3 comprising the amino acid sequence QQSYSTPPT (SEQ ID NO: 19).

25. The bispecific IgG antibody according to claim 24 , wherein the first arm comprises a variable light chain that is at least 90% identical to the amino acid sequence:

DIQMTQSPSSLSASVGDRVTITCRASQSISSYLNWYQQKPGKAPKLLIYAASSLQSGV PSRFSGSGSGTDFTLTISSLQPEDFATYYCQQSYSTPPTFGQGTKVEIK (SEQ ID NO: 20).

26. The bispecific IgG antibody according to claim 25 , wherein the first arm comprises a variable light chain comprising the amino acid sequence:

DIQMTQSPSSLSASVGDRVTITCRASQSISSYLNWYQQKPGKAPKLLIYAASSLQSGV PSRFSGSGSGTDFTLTISSLQPEDFATYYCQQSYSTPPTFGQGTKVEIK (SEQ ID NO: 20).

27. The bispecific IgG antibody according to claim 21 , wherein said first and second arms comprise a common light chain.

28. The bispecific IgG antibody according to claim 21 , comprising a mutated CH2 and/or lower hinge domains wherein the binding of said bispecific antibody with Fcγ receptors is significantly reduced.

29. The bispecific IgG antibody according to claim 22 , wherein said mutated CH2 and/or lower hinge domains comprise amino acid substitution L235G and/or G236R.

30. The bispecific IgG according to claim 21 , wherein said second arm specifically recognizes CD3.

Assignments (5)
NOTICE OF GRANT OF SECURITY INTEREST IN PATENTS Recorded Jan 30, 2026
From: MERUS B.V.
To: WILMINGTON TRUST, NATIONAL ASSOCIATION
Reel/Frame 074562/0322 →
SECURITY INTEREST Recorded Jan 29, 2026
From: MERUS B.V.
To: MORGAN STANLEY SENIOR FUNDING, INC.
Reel/Frame 074532/0434 →
CHANGE OF ADDRESS Recorded Jun 9, 2017
From: MERUS N.V.
To: MERUS N.V.
Reel/Frame 042745/0056 →
CHANGE OF NAME Recorded Jun 1, 2016
From: MERUS B.V.
To: MERUS N.V.
Reel/Frame 039038/0866 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 23, 2013
From: BAKKER, ALEXANDER BERTHOLD HENDRIK; VAN LOO, PIETER FOKKO; LOGTENBERG, TON
To: MERUS B.V.
Reel/Frame 031840/0980 →
Continuity (3)
Provisional Application 61706543 · Sep 27, 2012
Provisional Application 61834915 · Jun 14, 2013
Related Publication 20140120096A1 · May 1, 2014
Cited By (6)
US 12,195,551 US 12,247,078 US 12,600,784 US 12,606,604 US 12,622,976 US 12,668,638