IP Library Granted Patent US 8,877,197
Granted Patent B2
US 8,877,197 · App. 14/152,565 · Granted Nov 4, 2014

Anti-complement C1s

Inventors: Peter Van Vlasselaer (Portola Valley, CA); Graham Parry (South San Francisco, CA); Nancy E. Stagliano (South San Francisco, CA); Sandip Panicker (South San Francisco, CA)
Assignee: True North Therapeutics, Inc.
C07K16/40C07K2317/92C07K2317/24C07K16/18C07K2317/54C07K2317/35A61K2039/505C07K2317/55C07K2317/76
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Quick Facts
Patent No.
US 8,877,197
App. No.
14/152,565
Granted
Nov 4, 2014
Kind
B2
Abstract

The present disclosure provides antibodies that bind complement C1s protein; and nucleic acid molecules that encode such antibodies. The present disclosure also provides compositions comprising such antibodies, and methods to produce and use such antibodies, nucleic acid molecules, and compositions.

Claims (27)

1. A humanized antibody that binds complement C1s protein and comprises light chain CDRs of an antibody light chain variable region comprising amino acid sequence SEQ ID NO:7 and heavy chain CDRs of an antibody heavy chain variable region comprising amino acid sequence SEQ ID NO:8.

2. The humanized antibody of claim 1 , wherein the humanized antibody comprises a humanized light chain framework region.

3. The humanized antibody of claim 1 , wherein the humanized antibody comprises a humanized heavy chain framework region.

4. The humanized antibody of claim 1 , wherein the humanized antibody comprises a humanized light chain framework region and a humanized heavy chain framework region.

5. The humanized antibody of claim 1 , wherein the humanized antibody comprises a heavy chain constant region of the isotype IgG1, IgG2, IgG3, or IgG4.

6. The humanized antibody of claim 1 , wherein the humanized antibody is selected from the group consisting of a Fab fragment, a F(ab′) 2 fragment, a scFv, and a Fv.

7. A composition comprising: the humanized antibody of claim 1 ; and a pharmaceutically acceptable excipient.

8. The humanized antibody of claim 1 , wherein the humanized antibody comprises:

a) a light chain variable region comprising a complementarity-determining region (CDR) comprising a CDR-L1 having the amino acid sequence of SEQ ID NO:1, a CDR-L2 having the amino acid sequence of SEQ ID NO:2, a CDR-L3 having the amino acid sequence of SEQ ID NO:3; and

b) a heavy chain variable region comprising a CDR comprising a CDR-H1 having amino acid sequence SEQ ID NO:4, a CDR-H2 having amino acid sequence SEQ ID NO:5, and a CDR-H3 having amino acid sequence SEQ ID NO:6.

9. The humanized antibody of claim 8 , wherein the humanized antibody comprises a light chain variable region comprising the amino acid sequence of SEQ ID NO:44.

10. The humanized antibody of claim 8 , wherein the humanized antibody comprises a heavy chain variable region comprising the amino acid sequence of SEQ ID NO:42.

11. The humanized antibody of claim 8 , wherein the humanized antibody comprises a light chain variable region comprising the amino acid sequence of SEQ ID NO:44 and a heavy chain variable region comprising the amino acid sequence of SEQ ID NO:42.

12. The humanized antibody of claim 8 , wherein the humanized antibody comprises a humanized light chain framework region.

13. The humanized antibody of claim 8 , wherein the humanized antibody comprises a humanized heavy chain framework region.

14. The humanized antibody of claim 8 , wherein the humanized antibody comprises a humanized light chain framework region and a humanized heavy chain framework region.

15. The humanized antibody of claim 8 , wherein the humanized antibody comprises a heavy chain constant region of the isotype IgG1, IgG2, IgG3, or IgG4.

16. A humanized antibody that specifically binds complement C1s protein, wherein the humanized antibody comprises a heavy chain variable region comprising the amino acid sequence of any one of SEQ ID NOs:39-42.

17. The humanized antibody of claim 16 , wherein the humanized antibody comprises a humanized light chain framework region.

18. The humanized antibody of claim 16 , wherein the humanized antibody comprises a humanized heavy chain comprising the amino acid sequence of SEQ ID NO:42.

19. The humanized antibody of claim 17 , wherein the humanized antibody comprises a humanized light chain comprising the amino acid sequence of SEQ ID NO:44.

20. The humanized antibody of claim 16 , wherein the humanized antibody comprises a heavy chain constant region of the isotype IgG1, IgG2, IgG3, or IgG4.

21. A humanized antibody that specifically binds complement C1s protein, wherein the humanized antibody comprises a light chain variable region comprising the amino acid sequence of any one of SEQ ID NOs:43-45 and a heavy chain variable region comprising the amino acid sequence of any one of SEQ ID NOs:39-42.

22. The humanized antibody of claim 21 , wherein the humanized antibody comprises a humanized light chain comprising the amino acid sequence of SEQ ID NO:44.

23. The humanized antibody of claim 21 , wherein the humanized antibody comprises a humanized heavy chain comprising the amino acid sequence of SEQ ID NO:42.

24. The humanized antibody of claim 21 , wherein the humanized antibody comprises a humanized light chain comprising the amino acid sequence of SEQ ID NO:44 and a humanized heavy chain comprising the amino acid sequence of SEQ ID NO:42.

25. The humanized antibody of claim 21 , wherein the humanized antibody comprises a heavy chain constant region of the isotype IgG1, IgG2, IgG3, or IgG4.

Assignments (2)
CHANGE OF NAME Recorded Oct 4, 2017
From: TRUE NORTH THERAPEUTICS, INC.
To: BIOVERATIV USA INC.
Reel/Frame 044126/0710 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 11, 2014
From: VAN VLASSELAER, PETER; PARRY, GRAHAM; STAGLIANO, NANCY E.; PANICKER, SANDIP
To: TRUE NORTH THERAPEUTICS, INC.
Reel/Frame 032659/0887 →
Continuity (6)
Continuation 14070186 · Nov 1, 2013
Provisional Application 61721916 · Nov 2, 2012
Provisional Application 61754123 · Jan 18, 2013
Provisional Application 61779180 · Mar 13, 2013
Provisional Application 61846402 · Jul 15, 2013
Related Publication 20140127196A1 · May 8, 2014