IP Library Granted Patent US 11,279,771
Granted Patent B2
US 11,279,771 · App. 15/508,229 · Granted Mar 22, 2022

Antibodies capable of binding two epitopes on tissue factor pathway inhibitor (1-161)

Inventors: Helle Heibroch Petersen (Koebenhavn V, DK); Berit Olsen Krogh (Roedovre, DK); Jens Breinholt (Dyssegaerd, DK); Mikael Kofod-Hansen (Broenshoej, DK); Ida Hilden (Vanloese, DK)
Assignee: NOVO NORDISK A/S
C07K16/38A61K2039/507C07K2317/24C07K2317/31C07K2317/34C07K2317/53C07K2317/55C07K2317/56C07K2317/565C07K2317/76C07K2317/92
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Quick Facts
Patent No.
US 11,279,771
App. No.
15/508,229
Granted
Mar 22, 2022
Kind
B2
Abstract

The application discloses bispecific TFPI antibodies that are capable of specifically and simultaneously binding two epitopes within TFPI (1-161). Such bispecific antibodies strongly enhance thrombin generation by neutralising TFPI, even where the concentration of TFPI is elevated. Bispecific antibodies of the invention or compositions comprising them may be used for the treatment of subjects with a coagulopathy.

Claims (22)

1. A bispecific antibody capable of specifically binding a first epitope within positions 1-76 and a second epitope within positions 77-161 of human Tissue Factor Pathway Inhibitor (TFPI) (SEQ ID NO:1),

wherein the heavy chain of the first antigen recognition site comprises:

a complementary determining region (CDR) 1 sequence corresponding to amino acids 31 to 35 of SEQ ID NO: 6 (NYGVH); and

a CDR2 sequence corresponding to amino acids 50 to 65 of SEQ ID NO: 6 (VIWRGGSIDYNAAFMS); and

a CDR3 sequence corresponding to amino acids 98 to 110 of SEQ ID NO: 6 (NSHGNYVGYAMDY); and

wherein the light chain of the first antigen recognition site comprises:

a CDR1 sequence corresponding to amino acids 24 to 34 of SEQ ID NO: 7 (KASQSVGPAVA); and

a CDR2 sequence corresponding to amino acids 50 to 56 of SEQ ID NO: 7 (SASNRYT); and

a CDR3 sequence corresponding to amino acids 89 to 96 of SEQ ID NO: 7 (QQYTSYPT); and

wherein the heavy chain of the second antigen recognition site comprises:

a CDR1 sequence corresponding to amino acids 31 to 35 (NYAMS) of SEQ ID NO:19; and

a CDR2 sequence corresponding to amino acids 50 to 66 SEQ ID NO: 25 (TISRSGSYSYYADSVKG); and

a CDR3 sequence corresponding to amino acids 99 to 110 (LGGYDEGDAMDS) of SEQ ID NO:19; and

wherein the light chain of the second antigen recognition site comprises:

a CDR1 sequence corresponding to amino acids 24 to 39 (KSSQSLLESDGKTYLN) of SEQ ID NO: 20; and

a CDR2 sequence corresponding to amino acids 55 to 61 (LVSILDS) of SEQ ID NO: 20; and

a CDR3 sequence corresponding to amino acids 94 to 102 (LQATHFPQT) of SEQ ID NO: 20.

2. The bispecific antibody according to claim 1 , wherein the bispecific antibody is a bispecific Fab-Fab conjugate (BiFab).

3. A method of treating a coagulopathy in a subject in need thereof comprising administering the bispecific antibody according to claim 1 to said subject.

4. The method of claim 3 , wherein the coagulopathy is haemophilia A or B, with or without inhibitors.

5. The bispecific antibody of claim 1 , which is humanized or human.

6. The bispecific antibody of claim 1 , which is a full-length bispecific antibody or a chemical conjugate of two antigen binding fragments.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 3, 2017
From: PETERSEN, HELLE HEIBROCH; KROGH, BERIT OLSEN; BREINHOLT, JENS; KOFOD-HANSEN, MIKAEL; HILDEN, IDA
To: NOVO NORDISK A/S
Reel/Frame 042222/0179 →
Priority Claims (1)
EP 14185138 · Sep 17, 2014 · regional
Continuity (1)
Related Publication 20170260289A1 · Sep 14, 2017