Antibodies for the prevention or the treatment of bleeding episodes

Patent metadata

Field	Value
Publication number	US-10544231-B2
Application number	US-201515303889-A
Country	US
Kind code	B2
Filing date	Apr 16, 2015
Priority date	Apr 16, 2014
Publication date	Jan 28, 2020
Grant date	Jan 28, 2020

Abstract

The invention relates to an isolated monoclonal antibody that specifically binds to the D4 domain of VWF, competes for binding to VWF D4 domain with ADAMTS13 and partially inhibits ADAMTS 13-mediated degradation of VWF. More particularly, the invention relates to an isolated monoclonal antibody comprising a heavy chain wherein the variable domain comprises at least one CDR having a sequence selected from the group consisting of SEQ ID NO: 3 for H-CDR1, SEQ ID NO: 4 for H-CDR2 and SEQ ID NO: 5 for H-CDR3 and a light chain wherein the variable domain comprises at least one CDR having a sequence selected from the group consisting of SEQ ID NO: 7 for L-CDR1, SEQ ID NO: 8 for L-CDR2 and SEQ ID NO: 9 for L-CDR3. Antibodies of the invention are presented to be useful in for the prevention or the treatment of bleeding episodes, such as bleeding episodes occurring in patients with aortic stenosis or patients with ventricular assist devices (VAD).

First claim

The invention claimed is:

1. An isolated monoclonal antibody that specifically binds to a peptide of SEQ ID NO: 1 derived from the D4 domain of human von Willebrand factor (VWF), which competes for binding to VWF D4 domain with A Disintegrin And Metalloprotease with ThmmboSpondin domains-13 (ADAMTS13) and inhibits between 50 and 80% of ADAMTS13-mediated degradation of high molecular weight (HMW)-multimers of VWF, wherein a heavy chain variable region comprises
i) an amino acid sequence as set forth in SEQ ID NO:2,
or
ii) an H-CDR1, having an amino acid sequence as set forth in SEQ ID NO:3; an H-CDR2, having an amino acid sequence as set forth in SEQ ID NO:4; and an H-CDR3, having an amino acid sequence as set forth in SEQ ID NO:5;

and
a light chain variable region comprises
iii) an amino acid sequence as set forth in SEQ ID NO:6,
or
iv) a L-CDR1, having an amino acid sequence as set forth in SEQ ID NO:7; a L-CDR2, having an amino acid sequence as set forth in SEQ ID NO:8; and a L-CDR3, having an amino acid sequence as set forth in SEQ ID NO:9.

2. The antibody according to claim 1 , wherein the heavy chain variable region of said antibody has the amino acid sequence as set forth in SEQ ID NO: 2 and the light chain variable region has the amino acid sequence as set forth in SEQ ID NO: 6.

3. The antibody according to claim 1 , which is a chimeric antibody.

4. The antibody according to claim 1 , which is a humanized antibody.

5. A fragment of a monoclonal antibody that specifically binds to a peptide of SEQ ID NO: 1 derived from the D4 domain of human von Willebrand factor (VWF), competes for binding to VWF D4 domain with A Disintegrin And Metalloprotease with ThromboSpondin domains-13 (ADAMTS13) and inhibits between 50 and 80% of ADAMTS13-mediated degradation of high molecular weight (HMW)-multimers of VWF, wherein the fragment is selected from the group consisting of Fv, Fab, F(ab′)2, Fab′, dsFv, scFv, sc(Fv)2 and diabodies, wherein the fragment comprises: a heavy chain variable region comprising
i) an amino acid sequence as set forth in SEQ ID NO:2,
or
ii) an H-CDR1, having an amino acid sequence as set forth in SEQ ID NO:3; an H-CDR2, having an amino acid sequence as set forth in SEQ ID NO:4; and an H-CDR3, having an amino acid sequence as set forth in SEQ IC ID NO:5;

and
a light chain variable region comprising
iii) an amino acid sequence as set forth in SEQ ID NO:6,
or
iv) a L-CDR1, having an amino acid sequence as set forth in SEQ ID NO:7; a L-CDR2, having an amino acid sequence as set forth in SEQ ID NO:8; and a L-CDR3, having an amino acid sequence as set forth in SEQ ID NO:9.

6. A pharmaceutical composition comprising a monoclonal antibody that specifically binds to a peptide of SEQ ID NO: 1 derived from the D4 domain of human von Willebrand factor (VWF), which competes for binding to VWF D4 domain with A Disintegrin And Metalloprotease with ThromboSpondin domains-13 (ADAMTS13) and inhibits between 50 and 80% of ADAMTS13-mediated degradation of high molecular weight (HMW)-multimers of VWF; or a fragment of the monoclonal antibody, wherein the monoclonal antibody or the fragment of the monoclonal antibody comprises:
a heavy chain variable region comprising
i) an amino acid sequence as set forth in SEQ ID NO:2,
or
ii) an H-CDR1, having an amino acid sequence as set forth in SEQ ID NO:3; an H-CDR2, having an amino acid sequence as set forth in SEQ ID NO:4; and an H-CDR3, having an amino acid sequence as set forth in SEQ ID NO:5;

and
a light chain variable region comprising
iii) an amino acid sequence as set forth in SEQ ID NO:6,
or
iv) a L-CDR1, having an amino acid sequence as set forth in SEQ ID NO:7; a L-CDR2, having an amino acid sequence as set forth in SEQ ID NO:8; and a L-CDR3, having an amino acid sequence as set forth in SEQ ID NO:9.

7. The antibody of claim 3 , which is a chimeric mouse/human antibody.

8. The pharmaceutical composition of claim 6 wherein the fragment of the monoclonal antibody that specifically binds to the D4 domain of human von Willebrand factor (VWF), competes for binding to VWF D4 domain with A Disintegrin and Metalloprotease with ThromboSpondin domains-13 (ADAMTS13) and inhibits between 50 and 80% of ADAMTS13-mediated degradation of high molecular weight (HMW)-multimers of VWF, wherein the fragment is selected from the group consisting of Fv, Fab, F(ab′)2, Fab′, dsFv, scFv, sc(Fv)2 and diabodies.

9. The pharmaceutical composition of claim 6 wherein the antibody comprises the heavy chain variable region having the amino acid sequence as set forth in SEQ ID NO: 2 and the light chain variable region having the amino acid sequence as set forth in SEQ ID NO: 6.

10. The pharmaceutical composition of claim 6 wherein the antibody is a chimeric antibody.

11. The pharmaceutical composition of claim 6 wherein the antibody is a humanized antibody.

Assignees

• Inst Nat Sante Rech Med
• Univ Paris—Sud
• Centre Hospitalier Regional Univ Lille
• Univ De Droit Et De La Sante De Lille 2

Inventors

• Lenting Petrus
• DENIS Cécile
• Christophe Olivier
• Legendre Paulette
• Rauch Antoine
• Susen Sophie

Classifications

• A61P7/04

  Antihaemorrhagics; Procoagulants; Haemostatic agents; Antifibrinolytic agents · CPC title

• C07K2317/34

  Identification of a linear epitope shorter than 20 amino acid residues or of a conformational epitope defined by amino acid residues · CPC title

• C07K16/36 Primary

  against blood coagulation factors · CPC title

• C07K2317/24

  containing regions, domains or residues from different species, e.g. chimeric, humanized or veneered · CPC title

• C07K2317/70

  characterized by effect upon binding to a cell or to an antigen · CPC title