IP Library › Granted Patent US 9,220,775
Granted Patent B2
US 9,220,775 · App. 14/359,864 · Granted Dec 29, 2015

Binding molecules specific for HER3 and uses thereof

Inventors: Partha S. Chowdhury (Gaithersburg, MD); David Tice (Gaithersburg, MD); Zhan Xiao (Boyds, MD); Philipp Steiner (Washington, DC); Krista Kinneer (Montgomery Village, MD); Marlon Rebelatto (Gaithersburg, MD)
Assignee: MedImmune LLC
A61K39/39558A61K45/06C07K16/2863C07K16/32G01N33/57492A61K2039/505A61K2039/507C07K2317/21C07K2317/33C07K2317/55C07K2317/56C07K2317/565C07K2317/567C07K2317/73C07K2317/76C07K2317/77C07K2317/92
View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 9,220,775
App. No.
14/359,864
Granted
Dec 29, 2015
Kind
B2
Abstract

The present invention relates to antibodies and antigen binding fragments thereof that bind the extracellular domain of the HER3 receptor and inhibit various HER3 receptor related functions via ligand-dependent and/or ligand-independent mechanisms. Also provided are compositions with increased half-life. In addition, the invention provides compositions and methods for diagnosing and treating diseases associated with HER3 mediated signal transduction.

Claims (63)

1. An isolated antibody or an antigen-binding fragment thereof, which specifically binds to HER3, comprising an antibody variable light chain region (VL) and an antibody variable heavy chain region (VH), wherein the VL comprises the amino acid sequence:

[FW1]SGSLSNIGLNYVS 

(SEQ ID NO: 19)

[FW2]RNNQRPS 

(SEQ ID NO: 21)

[FW3]AAWDDSPPGEA 

(SEQ ID NO: 23)

[FW4]

wherein [FW1], [FW2], [FW3] and [FW4] represent VL framework regions, and

wherein the VH comprises the amino acid sequence:

[FW5]YYYMQ 

(SEQ ID NO: 31)

[FW6]YIGSSGGVTNYADSVKG 

(SEQ ID NO: 32)

[FW7]VGLGDAFDI 

(SEQ ID NO: 35)

[FW8]

wherein [FW5], [FW6], [FW7] and [FW8] represent VH framework regions.

2. The antibody or antigen-binding fragment of claim 1 , wherein the VL comprises an amino acid sequence at least 80% identical to the amino acid sequence of SEQ ID NO: 3, and wherein the VH comprises an amino acid sequence at least 80% identical to the amino acid sequence of SEQ ID NO: 2.

3. The antibody or antigen-binding fragment of claim 1 , wherein the VL comprises an amino acid sequence at least 90% identical to the amino acid sequence of SEQ ID NO: 3, and wherein the VH comprises an amino acid sequence at least 90% identical to the amino acid sequence of SEQ ID NO: 2.

4. The antibody or antigen-binding fragment of claim 1 , wherein the VL comprises an amino acid sequence at least 95% identical to the amino acid sequence of SEQ ID NO: 3, and wherein the VH comprises an amino acid sequence at least 95% identical to the amino acid sequence of SEQ ID NO: 2.

5. The antibody or antigen-binding fragment thereof of claim 1 , wherein FW1 comprises SEQ ID NO: 40 or 44, FW2 comprises SEQ ID NO: 41, FW3 comprises SEQ ID NO: 42, FW4 comprises SEQ ID NO: 43, FW5 comprises SEQ ID NO: 36, FW6 comprises SEQ ID NO: 37, FW7 comprises SEQ ID NO: 38 and FW8 comprises SEQ ID NO: 39.

6. The antibody or antigen-binding fragment thereof of claim 1 , which comprises a VL comprising SEQ ID NO: 3 and a VH comprising SEQ ID NO: 2.

7. The antibody or antigen-binding fragment thereof of claim 1 , which comprises a heavy chain constant region.

8. The antibody or antigen-binding fragment thereof of claim 7 , wherein the heavy chain constant region is a human IgG constant region.

9. The antibody or antigen-binding fragment thereof of claim 8 , wherein the human IgG constant region is an IgG1 constant region.

10. The antibody or antigen-binding fragment of claim 8 ,

(i) wherein the human IgG constant region comprises amino acid substitutions relative to a wild-type human IgG constant domain at positions 252, 254, and 256, wherein the numbering is according to the EU index as set forth in Kabat, and wherein

(a) the amino acid at position 252 Methionine) is substituted with Tyrosine (Y),

(b) the amino acid at position 254 (Serine) is substituted with Threonine (T), and

(c) the amino acid at position 256 (Threonine) is substituted with Glutamic acid (E).

11. The antibody or antigen-binding fragment thereof of claim 9 , which comprises a light chain constant region selected from the group consisting of a human kappa constant region and a human lambda constant region.

12. The antibody or antigen-binding fragment thereof of claim 11 , which comprises a human lambda constant region.

13. The antibody or antigen-binding fragment thereof of claim 1 , which comprises a light chain constant region selected from the group consisting of a human kappa constant region and a human lambda constant region.

14. The antibody or antigen-binding fragment of claim 1 , wherein the antibody is a human antibody, a humanized antibody, a chimeric antibody, a recombinant antibody, a multispecific antibody, or an antigen-binding fragment thereof; wherein the antigen-binding fragment is an Fv, Fab, F(ab′)2, Fab′, dsFv, scFv, or sc(Fv)2; or wherein the antibody or antigen-binding fragment thereof is conjugated to at least one heterologous agent.

15. The antibody or antigen-binding fragment of claim 1 , wherein the antibody is a monoclonal antibody.

16. The antibody or antigen-binding fragment thereof of claim 1 , comprising (i) an antibody light chain comprising an antibody VL comprising SEQ ID NO: 3 and a human lambda light chain constant region, and (ii) an antibody heavy chain comprising an antibody VH comprising SEQ ID NO: 2 and a human IgG1 heavy chain constant region, wherein the human IgG1 constant region comprises amino acid substitutions relative to a wild-type human IgG1 constant domain at positions 252, 254, and 256, wherein the numbering is according to the EU index as set forth in Kabat, and wherein

(a) the amino acid at position 252 (Methionine) is substituted with Tyrosine (Y),

(b) the amino acid at position 254 (Serine) is substituted with Threonine (T), and

(c) the amino acid at position 256 (Threonine) is substituted with Glutamic acid (E).

17. The antibody of claim 16 , wherein the antibody is a monoclonal antibody.

18. The antibody of claim 14 , wherein the antibody is a human antibody.

19. The antibody of claim 16 , wherein the antibody is a human antibody.

20. The antibody of claim 17 , wherein the antibody is a human antibody.

21. A composition comprising the antibody or antigen-binding fragment thereof of claim 1 , and a pharmaceutically acceptable carrier.

22. The composition of claim 21 , wherein the composition is refrigerator stable, wherein the antibody or antigen-binding fragment thereof is at a concentration of 25-100 mg/mL, and wherein the composition further comprises 25 mM histidine/histidine HCl, 205 mM sucrose, and 0.02% polysorbate 80 at pH 6.0.

23. A composition comprising the antibody of claim 16 , and a pharmaceutically acceptable carrier.

24. A kit comprising the antibody or antigen-binding fragment thereof of claim 1 for use in inhibiting the proliferation of a cell expressing HER3, wherein said cell is a human head and neck tumor cell, a human non-small cell lung cancer cell, a human colorectal tumor cell, a human prostate tumor cell, or a human breast cancer cell.

25. An isolated nucleic acid comprising a sequence encoding the antibody or antigen-binding fragment according to claim 1 .

26. An isolated vector comprising a nucleic acid according to claim 25 .

27. An in vitro host cell comprising a nucleic acid sequence according to claim 25 .

28. A method of making an antibody or antigen-binding fragment thereof, comprising (a) culturing a cell comprising the nucleic acid of claim 25 ; and (b) isolating the antibody or antigen-binding fragment thereof.

29. A method of inhibiting the proliferation of a cell expressing HER3, said method comprising contacting the cell with the antibody or antigen-binding fragment of claim 1 , wherein said cell is a human head and neck tumor cell, a human non-small cell lung cancer cell, a human colorectal tumor cell, a human prostate tumor cell, or a human breast cancer cell.

30. The method of claim 29 , wherein the inhibition of cell proliferation occurs in vivo.

31. A method of inhibiting the in vivo proliferation of a cell expressing HER3, said method comprising contacting the cell with the antibody or antigen-binding fragment of claim 6 , wherein said cell is a human head and neck tumor cell, a human non-small cell lung cancer cell, a human colorectal tumor cell, a human prostate tumor cell, or a human breast cancer cell.

32. A method of inhibiting the in vivo proliferation of a cell expressing HER3, said method comprising contacting the cell with the antibody or antigen-binding fragment of claim 11 , wherein said cell is a human head and neck tumor cell, a human non-small cell lung cancer cell, a human colorectal tumor cell, a human prostate tumor cell, or a human breast cancer cell.

33. A method of inhibiting the in vivo proliferation of a cell expressing HER3, said method comprising contacting the cell with the antibody or antigen-binding fragment of claim 10 , wherein said cell is a human head and neck tumor cell, a human non-small cell lung cancer cell, a human colorectal tumor cell, a human prostate tumor cell, or a human breast cancer cell.

34. A method of inhibiting the proliferation of a cell expressing HER3, said method comprising contacting the cell with the antibody or antigen-binding fragment of claim 16 , wherein said cell is a human head and neck tumor cell, a human non-small cell lung cancer cell, a human colorectal tumor cell, a human prostate tumor cell, or a human breast cancer cell.

35. The method of claim 34 , wherein the inhibition of cell proliferation occurs in vivo.

36. A method of inhibiting the proliferation of a cell expressing HER3, said method comprising contacting the cell with the antibody or antigen-binding fragment of claim 17 , wherein said cell is a human head and neck tumor cell, a human non-small cell lung cancer cell, a human colorectal tumor cell, a human prostate tumor cell, or a human breast cancer cell.

37. The method of claim 36 , wherein the inhibition of cell proliferation occurs in vivo.

38. A method of inhibiting the proliferation of a cell expressing HER3, said method comprising contacting the cell with the antibody or antigen-binding fragment of claim 20 , wherein said cell is a human head and neck tumor cell, a human non-small cell lung cancer cell, a human colorectal tumor cell, a human prostate tumor cell, or a human breast cancer cell.

39. The method of claim 38 , wherein the inhibition of cell proliferation occurs in vivo.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 8, 2014
From: CHOWDHURY, PARTHA S.; KINNEER, KRISTA; XIAO, ZHAN; REBELATTO, MARLON; STEINER, PHILIPP; TICE, DAVID
To: MEDIMMUNE, LLC
Reel/Frame 034421/0587 →
Continuity (4)
Provisional Application 61563092 · Nov 23, 2011
Provisional Application 61656670 · Jun 7, 2012
Provisional Application 61722558 · Nov 5, 2012
Related Publication 20140363429A1 · Dec 11, 2014