IP Library Granted Patent US 10,201,586
Granted Patent B2
US 10,201,586 · App. 15/373,742 · Granted Feb 12, 2019

TFPI inhibitors and methods of use

Inventors: Michael Dockal (Vienna, AT); Rudolf Hartmann (Bisamberg, AT); Markus Fries (Vienna, AT); Friedrich Scheiflinger (Vienna, AT); Hartmut Ehrlich (Paris, FR); Ulrich Reineke (Berlin, DE); Frank Osterkamp (Berlin, DE); Thomas Polakowski (Berlin, DE)
Assignees: Baxalta GmbH; Baxalta Incorporated
A61K38/10C07K1/14C07K7/08C07K14/00C07K14/8114G01N33/68G06F19/16G06F19/18A61K38/00A61K2121/00G01N2333/745G01N2333/8114G01N2333/96444G01N2333/96447G01N2500/02G01N2500/04G01N2500/20
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Quick Facts
Patent No.
US 10,201,586
App. No.
15/373,742
Granted
Feb 12, 2019
Kind
B2
Abstract

The invention provides peptides that bind Tissue Factor Pathway Inhibitor (TFPI), including TFPI-inhibitory peptides, and compositions thereof. The peptides may be used to inhibit a TFPI, enhance thrombin formation in a clotting factor-deficient subject, increase blood clot formation in a subject, treat a blood coagulation disorder in a subject, purify TFPI, an identify a TFPI-binding compound.

Claims (17)

1. A peptide comprising (a) an amino acid sequence having at least 80% identity to SYYKWH[CA-Moo-RDLKGTFTC]VWVKF (SEQ ID NO: 1334) or (b) a variant of SEQ ID NO: 1334, wherein the variant comprises one or two amino acid substitution(s), deletion(s) or insertion(s).

2. The peptide of claim 1 , further comprising N-terminal amino acid(s) and/or moieties selected from the group consisting of FAM-Ttds, PE, Palm, 2-phenyl acetyl, 3-phenyl propionyl, 2-(naphtha-2-yl)acetyl, hexanoyl, 2-methyl propionyl, 3-methyl butanoyl, 2-naphthylsulfonyl, and 1-naphthylsulfonyl.

3. The peptide of claim 1 , further comprising C-terminal amino acid(s) and/or moieties selected from the group consisting of C, c, C(NEM), K(Ttds-maleimidopropionyl(EtSH)), FA19205, FA19204, FA19203, FA03202, K(Tdts-maleimide), K(AOA), and Cea.

4. The peptide of claim 1 , wherein the IC50 of the peptide is less than 250 nM or less than 50 nM and wherein the peptide comprises a disulfide bond between two cysteine residues.

5. The peptide of claim 1 , wherein the peptide inhibits TFPI activity and binds to TFPI 1-alpha with a dissociation constant of less than 10 μM and wherein the peptide comprises a disulfide bond between two cysteine residues.

6. The peptide of claim 1 , operably linked to a moiety that enhances the half-life of the peptide.

7. The peptide of claim 1 , wherein the peptide is conjugated to a polyethylene glycol (PEG) moiety, human serum albumin (HSA), an antibody or fragment thereof, hydroxyethyl starch, a multimer comprising proline, alanine, serine, or a combination thereof (PASylation), or a C12-C18 fatty acid.

8. The peptide of claim 1 , wherein the peptide comprises 90% identity to SEQ ID NO: 1334.

9. The peptide of claim 8 , wherein the peptide comprises SEQ ID NO: 1334.

10. The peptide of claim 8 , wherein the peptide consists of SEQ ID NO: 1334.

11. A TFPI-binding peptide comprising a homo-dimer, homo-multimer, hetero-dimer, or hetero-multimer of one or more peptides of claim 1 .

12. A pharmaceutical composition for treating a subject suffering from a blood coagulation disorder or at risk of suffering from a blood coagulation disorder, comprising the peptide according to claim 1 .

13. A pharmaceutical composition comprising the peptide of claim 1 and a pharmaceutically acceptable carrier.

14. A peptide complex comprising (i) the peptide of claim 1 and (ii) another peptide linked to the peptide of (i).

15. The peptide complex of claim 14 wherein peptide (i) is linked to peptide (ii) via a multimerization domain or chemical linkage.

16. The peptide complex of claim 14 , further comprising at least one moiety for improving peptide half life.

17. A pharmaceutical composition comprising the peptide complex of claim 14 for use in treating a subject suffering from a blood coagulation disorder or at risk of suffering from a blood coagulation disorder.

Assignments (7)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 31, 2021
From: BAXALTA GMBH; BAXALTA INCORPORATED
To: TAKEDA PHARMACEUTICAL COMPANY LIMITED
Reel/Frame 055189/0238 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 24, 2018
From: DOCKAL, MICHAEL; HARTMANN, RUDOLF; FRIES, MARKUS; SCHEIFLINGER, FRIEDRICH; EHRLICH, HARTMUT
To: BAXTER INTERNATIONAL INC.; BAXTER HEALTHCARE SA
Reel/Frame 047136/0086 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 24, 2018
From: 3B PHARMACEUTICALS GMBH
To: BAXTER INTERNATIONAL INC.; BAXTER HEALTHCARE SA
Reel/Frame 047136/0091 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 24, 2018
From: REINEKE, ULRICH; OSTERKAMP, FRANK; POLAKOWSKI, THOMAS
To: 3B PHARMACEUTICALS GMBH
Reel/Frame 046953/0919 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 24, 2018
From: BAXTER INTERNATIONAL INC.
To: BAXALTA GMBH; BAXALTA INCORPORATED
Reel/Frame 047622/0265 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 24, 2018
From: BAXTER HEALTHCARE SA
To: BAXALTA GMBH; BAXALTA INCORPORATED
Reel/Frame 047136/0195 →
CHANGE OF ADDRESS Recorded Oct 30, 2017
From: BAXALTA GMBH
To: BAXALTA GMBH
Reel/Frame 044322/0730 →
Continuity (5)
Continuation 14677581 · Apr 2, 2015
Continuation 13846359 · Mar 18, 2013
Division 13026070 · Feb 11, 2011
Provisional Application 61315758 · Mar 19, 2010
Related Publication 20170157198A1 · Jun 8, 2017
Cited By (3)
US 12,370,125 US 12,414,899 US 12,427,210