IP Library Granted Patent US 9,365,648
Granted Patent B1
US 9,365,648 · App. 15/044,552 · Granted Jun 14, 2016

Methods of using anti-CGRP antagonist antibodies

Inventors: Joerg Zeller (Ann Arbor, MI); Kristian T. Poulsen (San Francisco, CA); Yasmina Noubia Abdiche (Mountain View, CA); Jaume Pons (San Bruno, CA); Sierra Jones Collier (Menlo Park, CA); Arnon Rosenthal (Woodside, CA)
Assignee: LABRYS BIOLOGICS, INC.
C07K16/26A61K2039/505C07K2317/21C07K2317/24C07K2317/34C07K2317/52C07K2317/55C07K2317/56C07K2317/565C07K2317/71C07K2317/76C07K2317/92C07K2317/94
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Quick Facts
Patent No.
US 9,365,648
App. No.
15/044,552
Granted
Jun 14, 2016
Kind
B1
Abstract

The invention features methods for preventing or treating CGRP associated disorders such as vasomotor symptoms, including headaches (e.g., migraine, cluster headache, and tension headache) and hot flushes, by administering an anti-CGRP antagonist antibody. Antagonist antibody G1 and antibodies derived from G1 directed to CGRP are also described.

Claims (29)

1. A method for reducing incidence of or treating cluster headache in an individual, comprising administering to the individual an effective amount of an anti-CGRP antagonist antibody, wherein the anti-CGRP antagonist antibody is a human or humanized antibody that blocks or decreases cyclic adenosine monophosphate (cAMP) activation in cells.

2. The method of claim 1 , wherein the anti-CGRP antagonist antibody has a binding affinity (K D ) to human α-CGRP of 50 nM or less as measured by surface plasmon resonance at 37° C.

3. The method of claim 1 , wherein the anti-CGRP antagonist antibody has a binding affinity (K D ) to human α-CGRP of 10 nM or less as measured by surface plasmon resonance at 37° C.

4. The method of claim 1 , wherein the anti-CGRP antagonist antibody has a binding affinity (K D ) to human α-CGRP of 1 nM or less as measured by surface plasmon resonance at 37° C.

5. The method of claim 1 , wherein the anti-CGRP antagonist antibody has a binding affinity (K D ) to human α-CGRP of 500 pM or less as measured by surface plasmon resonance at 37° C.

6. The method of claim 1 , wherein the anti-CGRP antagonist antibody has a binding affinity (K D ) to human α-CGRP of 100 pM or less as measured by surface plasmon resonance at 37° C.

7. The method of claim 1 , wherein the anti-CGRP antagonist antibody has a binding affinity (K D ) to human α-CGRP of 50 pM or less as measured by surface plasmon resonance at 37° C.

8. The method of claim 1 , wherein the anti-CGRP antagonist antibody is a humanized antibody.

9. The method of claim 1 , wherein the anti-CGRP antagonist antibody comprises a heavy chain constant region selected from the group consisting of: IgG, IgM, IgD, IgA and IgE.

10. The method of claim 1 , wherein the anti-CGRP antagonist antibody comprises a heavy chain constant region derived from an IgG1 constant region.

11. The method of claim 1 , wherein the anti-CGRP antagonist antibody comprises a heavy chain constant region derived from an IgG2 constant region.

12. The method of claim 1 , wherein the anti-CGRP antagonist antibody comprises a heavy chain constant region derived from an IgG3 constant region.

13. The method of claim 1 , wherein the anti-CGRP antagonist antibody comprises a heavy chain constant region derived from an IgG4 constant region.

14. The method of claim 1 , wherein the anti-CGRP antagonist antibody comprises an Fc region with an impaired effector function.

15. The method of claim 1 , wherein the anti-CGRP antagonist antibody binds a C-terminal fragment having amino acids 25-37 of human α-CGRP.

16. The method of claim 1 , wherein the anti-CGRP antagonist antibody binds a C-terminal epitope within amino acids 25-37 of human α-CGRP.

17. The method of claim 1 , wherein the anti-CGRP antagonist antibody is: (a) an antibody having a CDR H1 as set forth in SEQ ID NO: 3; a CDR H2 as set forth in SEQ ID NO: 4; a CDR H3 as set forth in SEQ ID NO: 5; a CDR L1 as set forth in SEQ ID NO: 6; a CDR L2 as set forth in SEQ ID NO: 7; and a CDR L3 as set forth in SEQ ID NO: 8; or (b) a variant of an antibody according to (a) as shown in Table 6.

18. The method of claim 1 , wherein the anti-CGRP antagonist antibody comprises a V H domain that is at least 90% identical in amino acid sequence to SEQ ID NO: 1 and a V L domain that is at least 90% identical in amino acid sequence to SEQ ID NO: 2.

19. The method of claim 1 , wherein the anti-CGRP antagonist antibody comprises a V H domain comprising SEQ ID NO: 1 and a V L domain comprising SEQ ID NO: 2.

20. The method of claim 1 , wherein the anti-CGRP antagonist antibody comprises a heavy chain sequence of SEQ ID NO: 11 and a light chain sequence of SEQ ID NO: 12.

21. The method of claim 1 , wherein the anti-CGRP antagonist antibody comprises a light chain produced by an expression vector with ATCC Accession No. PTA-6866.

22. The method of claim 1 , wherein the anti-CGRP antagonist antibody comprises a heavy chain produced by an expression vector with ATCC Accession No. PTA-6867.

23. The method of claim 1 , wherein the individual is human.

24. The method of claim 1 , wherein route of administration of the anti-CGRP antagonist antibody is selected from the group consisting of systemically, intravenously, subcutaneously, intramuscularly, and transdermally.

25. The method of claim 1 , wherein a dose of the anti-CGRP antagonist antibody is at least about 3 μg/kg.

26. The method of claim 1 , wherein the anti-CGRP antagonist antibody is formulated with a pharmaceutically acceptable carrier, excipient, and/or stabilizer.

27. The method of claim 1 , wherein the anti-CGRP antagonist antibody blocks CGRP from binding to its receptor.

28. The method of claim 1 , wherein the anti-CGRP antagonist antibody blocks elicitation of a cellular response to CGRP.

29. The method of claim 1 , wherein the cells are SK-N-MC cells.

Assignments (3)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 21, 2016
From: LABRYS BIOLOGICS, INC.
To: TEVA PHARMACEUTICALS INTERNATIONAL GMBH
Reel/Frame 040449/0698 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 16, 2016
From: ZELLER, JÖRG; POULSEN, KRISTIAN T.; ABDICHE, YASMINA N.; PONS, JAUME; JONES, SIERRA L.; ROSENTHAL, ARNON
To: RINAT NEUROSCIENCE CORP.
Reel/Frame 037746/0077 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 16, 2016
From: RINAT NEUROSCIENCE CORP.
To: LABRYS BIOLOGICS, INC.
Reel/Frame 037746/0090 →
Continuity (7)
Continuation 14719015 · May 21, 2015
Continuation 14251925 · Apr 14, 2014
Continuation 14086816 · Nov 21, 2013
Continuation 13870871 · Apr 25, 2013
Continuation 13179846 · Jul 11, 2011
Division 12093638
Provisional Application 60736623 · Nov 14, 2005