IP Library Granted Patent US 8,119,135
Granted Patent B2
US 8,119,135 · App. 12/355,689 · Granted Feb 21, 2012

Antibodies which bind to epitopes of glycoprotein VI

Assignees: Helmhotz Zentrum Munchen, Deutsches Forschungszentrum fur Gesundheit und Umwelt (GmbH); Corimmun GmbH
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Quick Facts
Patent No.
US 8,119,135
App. No.
12/355,689
Granted
Feb 21, 2012
Kind
B2
Abstract

The present invention provides anti-thrombotic agents, methods for screening for said anti-thrombotics agents and methods of treating thrombotic and other cardiovascular disorders.

Claims (44)

1. A pharmaceutical formulation comprising

a monoclonal antibody secreted by the hGP 5C4 cell line deposited with DSMZ-Deutsche Sammlung von Mikroorganismen und Zellkulturen under Accession No. 2631, a humanized form of the monoclonal antibody, or an antigen binding fragment of the monoclonal antibody, wherein the monoclonal antibody, humanized form or antigen binding fragment specifically binds to glycoprotein VI; and

a pharmaceutically acceptable excipient.

2. The pharmaceutical formulation according to claim 1 , wherein glycoprotein VI is a human glycoprotein VI.

3. The pharmaceutical formulation according to claim 1 , comprising the monoclonal secreted by the hGP 5C4 cell line deposited with DSMZ-Deutsche Sammlung von Mikroorganismen und Zellkulturen under Accession No. 2631.

4. The pharmaceutical formulation according to claim 1 comprising the antigen binding fragment of the monoclonal antibody.

5. The pharmaceutical formulation comprising the antigen binding fragment of the monoclonal antibody according to claim 4 , wherein the antigen binding fragment is a Fab.

6. The pharmaceutical formulation according to claim 1 , comprising the humanized form of the monoclonal antibody.

7. A pharmaceutical formulation comprising a conjugate comprising an effector moiety and the monoclonal antibody, antigen binding fragments or humanized form of the monoclonal antibody, according to claim 1 , and a pharmaceutically acceptable excipient.

8. A hybridoma cell line deposited with DSMZ-Deutsche Sammlung von Mikroorganismen and Zellkulturen under Accession number 2631.

9. A method of treating thrombosis in a subject, comprising

administering to the subject a therapeutically effective amount of the pharmaceutical formulation of claim 1 or a pharmaceutical formulation comprising a conjugate of the antibody secreted by the hGP 5C4 cell line deposited with DSMZ-Deutsche Sammlung von Mikroorganismen and Zellkulturen under Accession No. 2631, a humanized form of the monoclonal antibody, or an antigen binding fragment of the monoclonal antibody and an effector molecule,

thereby treating the thrombosis in the subject.

10. The method of claim 9 , wherein the pharmaceutical formulation is formulated for parenteral administration.

11. An isolated monoclonal antibody comprising a heavy chain and a light chain variable domain, or an antigen binding fragment thereof or a humanized form thereof,

wherein the heavy chain comprises a heavy chain complementarity determining region (HCDR) 1 comprising Kabat position 31 to 35b of the amino acid sequence set forth as SEQ ID NO: 151, a HCDR2 comprising Kabat position 50 to 65, 95 to 102 of the amino acid sequence set forth as SEQ ID NO: 151, a HCDR3 comprising Kabat position 95 to 102 of the amino acid sequence set forth as SEQ ID NO: 151;

and wherein the light chain comprises light chain complementarity determining region (LCDR) 1 comprising Kabat position 24 to 34 of the amino acid sequence set forth as SEQ ID NO: 149, a LCDR 2 comprising Kabat position 50 to 56 of the amino acid sequence set forth as SEQ ID NO: 149, and a LCDR 3 comprising Kabat position 95-102 of the amino acid sequence set forth as SEQ ID NO: 149, and wherein the monoclonal antibody, the antigen binding fragment, and the humanized form specifically bind human glycoprotein IV.

12. The monoclonal antibody, the antigen binding fragment, or humanized form according to claim 11 , wherein the heavy chain variable domain comprises the amino acid sequence set forth as SEQ ID NO: 151, and wherein the light chain variable domain comprises the amino acid sequence set forth as SEQ ID NO: 149.

13. A pharmaceutical composition comprising the monoclonal antibody, the antigen binding fragment, or the humanized form according to claim 11 .

14. The humanized form of the monoclonal antibody according to claim 11 .

15. A monoclonal antibody produced by the hybridoma cell of claim 8 , an antigen binding fragment thereof or a humanized form thereof, wherein the monoclonal antibody, antigen binding fragment and humanized form specifically bind human glycoprotein IV.

16. An isolated monoclonal antibody secreted by the hGP 5C4 cell line deposited-with DSMZ-Deutsche Sammlung von Mikroorganismen and Zellkulturen under Accession No. 2631, a humanized form of the monoclonal antibody, or an antigen binding fragment of the monoclonal antibody, wherein the monoclonal antibody, humanized form or antigen binding fragment specifically binds to human glycoprotein VI.

17. The humanized form of the isolated monoclonal antibody according to claim 16 .

18. The antigen binding fragment of the isolate monoclonal antibody according to claim 16 .

19. The antigen binding fragment according to claim 16 , wherein the antigen binding fragment is a Fab fragment.

20. A conjugate comprising the monoclonal antibody, antigen binding fragment or humanized form according to claim 16 and an effector molecule.

21. The conjugate according to claim 20 , wherein the effector molecule is a label.

22. A method of inhibiting the aggregation and/or activation of human platelets, comprising

contacting the human platelets with an effective amount of the monoclonal antibody, humanized form, or antigen binding fragment according to claim 16 ,

thereby inhibiting the aggregation and/or activation of the human platelets.

23. A method of inhibiting the aggregation and/or activation of human platelets, comprising

contacting the human platelets with an effective amount of the pharmaceutical composition according to claim 1 ,

thereby inhibiting the aggregation and/or activation of the human platelets.

24. A method of inhibiting the aggregation and/or activation of human platelets, comprising

contacting the human platelets with an effective amount of the pharmaceutical composition according to claim 11 ,

thereby inhibiting the aggregation and/or activation of the human platelets.

25. The method of claim 24 , comprising

contacting the human platelets with an effective amount of the monoclonal antibody, humanized form or antigen binding fragment according to claim 11 ex vivo.

26. A method of treating thrombosis in a subject, comprising

administering to the subject a therapeutically effective amount of the monoclonal antibody, humanized form or antigen binding fragment according to claim 11 ,

thereby treating the thrombosis in the subject.

27. A method of treating thrombosis in a subject, comprising

administering to the subject a therapeutically effective amount of the monoclonal antibody, humanized form or antigen binding fragment according to claim 16 ,

thereby treating the thrombosis in the subject.

Assignments (4)
ASSET SALE AND TRANSFER AGREEMENT Recorded Sep 19, 2016
From: CORIMMUN GMBH
To: AVA VIER VERMOGENSVERWALTUNG GMBH
Reel/Frame 040073/0265 →
CHANGE OF NAME Recorded Sep 19, 2016
From: AVA VIER VERMOGENSVERWALTUNG GMBH
To: ADVANCECOR GMBH
Reel/Frame 039783/0293 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 29, 2011
From: MUNCH, GOTZ; BULTMANN, ANDREAS; GAWAZ, MEINRAD
To: CORIMMUN GMBH
Reel/Frame 027289/0864 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 29, 2011
From: KREMMER, ELISABETH
To: HELMHOTZ ZENTRUM MUNCHEN, DEUTSCHES FORSCHUNGSZENTRUM FUR GESUNDHEIT UND UMWELT (GMBH)
Reel/Frame 027289/0874 →
Priority Claims (3)
EP 02012742 · Jun 7, 2002 · regional
EP 03027772 · Dec 3, 2003 · regional
GB 0511590.2 · Jun 7, 2005 · national
Continuity (6)
Continuation 11446537 · Jun 2, 2006
Continuation In Part 11009106 · Dec 10, 2004
Continuation In Part 10489053
Continuation In Part 12355689
Continuation In Part PCTEP2004013779 · Dec 3, 2004
Related Publication 20100003244A1 · Jan 7, 2010