IP Library Granted Patent US 8,257,709
Granted Patent B2
US 8,257,709 · App. 12/533,552 · Granted Sep 4, 2012

Antibodies against

Assignees: University of Massachusetts; Medarex, Inc.
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 8,257,709
App. No.
12/533,552
Granted
Sep 4, 2012
Kind
B2
Abstract

Antibodies that specifically bind to toxins of C. difficile , antigen binding portions thereof, and methods of making and using the antibodies and antigen binding portions thereof are provided herein.

Claims (29)

1. An isolated monoclonal antibody that binds to Clostridium difficile ( C. difficile ) toxin B, or an antigen binding portion thereof, wherein the antibody binds to the same epitope of C. difficile toxin B recognized by an antibody comprising a heavy and light chain variable region having the amino acid sequences set forth in SEQ ID NOs: 54 and 58.

2. An isolated monoclonal antibody, or antigen binding portion thereof, that binds to C. difficile toxin B, wherein the antibody comprises a heavy chain variable region having the amino acid sequence set forth in SEQ ID NO:54.

3. An isolated monoclonal antibody, or antigen binding portion thereof, that binds to C. difficile toxin B, wherein the antibody comprises a light chain variable region having the amino acid sequence set forth in SEQ ID NO:58.

4. An isolated monoclonal antibody, or antigen binding portion thereof, that binds to C. difficile toxin B, wherein the antibody comprises heavy and light chain variable regions comprising the amino acid sequences set forth in SEQ ID NOs:54 and 58, respectively.

5. An isolated monoclonal antibody, or antigen binding portion thereof, that binds to C. difficile toxin B, wherein the antibody comprises:

(a) a heavy chain variable region CDR1 comprising SEQ ID NO:62;

(b) a heavy chain variable region CDR2 comprising SEQ ID NO:64;

(c) a heavy chain variable region CDR3 comprising SEQ ID NO:66;

(d) a light chain variable region CDR1 comprising SEQ ID NO:68;

(e) a light chain variable region CDR2 comprising SEQ ID NO:70; and

(f) a light chain variable region CDR3 comprising SEQ ID NO:72.

6. The isolated monoclonal antibody of claim 1 , wherein the antibody is a human antibody, a humanized antibody or a chimeric antibody.

7. The isolated monoclonal antibody of claim 1 , wherein the antigen binding portion of the antibody is a Fab, Fab′2, ScFv, Fd, Fv or dAb.

8. The isolated monoclonal antibody of claim 1 , wherein the K D of the antibody, or antigen binding portion thereof, is less than 20 ×10 −6 M.

9. A method of treating Clostridium difficile disease in a subject, the method comprising administering to the subject the antibody, or antigen binding portion thereof, of any one of the claim 1 - 4 , wherein C. difficile disease is treated in the subject.

10. The method of claim 9 wherein the subject is human.

11. The method of claim 9 , wherein the antibody, or antigen binding portion thereof, is administered intravenously, intramuscularly, or subcutaneously to the subject.

12. The method of claim 9 , wherein the antibody, or antigen binding portion thereof, is administered in combination with a second agent.

13. The method of claim 12 , wherein the second agent is a second antibody or antigen binding portion thereof.

14. The method of claim 12 , wherein the second agent is an antibiotic.

15. The method of claim 14 , wherein the second agent is vancomycin or metronidazole.

16. The isolated monoclonal antibody, or antigen binding portion thereof, of any one of claims 2 - 5 , wherein the antibody, or antigen binding portion thereof, binds to an epitope between amino acids 1777 and 2366 of C. difficile toxin B.

17. The isolated monoclonal antibody, or antigen binding portion thereof, of any one of claims 2 - 5 , wherein the antibody is a human antibody, a humanized antibody or a chimeric antibody.

18. The antigen binding port on of any one of claims 2 - 5 , wherein the antigen binding portion is a Fab, Fab′2, ScFv, Fd or dAb.

19. The isolated monoclonal antibody, or antigen binding portion thereof, of any one of claims 2 - 5 , wherein the K D of the antibody or antigen binding portion thereof is less than 20×10 −6 M.

20. The isolated monoclonal antibody, or antigen binding portion thereof, of any one of claims 2 - 5 , wherein the antibody or antigen binding portion thereof neutralizes toxin B in vitro or in vivo.

21. A composition comprising the isolated monoclonal antibody, or antigen binding portion thereof, of any one of claims 2 - 5 .

22. The composition of claim 21 further comprising an additional agent.

23. The composition of claim 22 wherein the additional agent is an antibody or an antibiotic.

Assignments (4)
MERGER Recorded Jun 3, 2015
From: MEDAREX, L.L.C.
To: E. R. SQUIBB & SONS, L.L.C.
Reel/Frame 035776/0116 →
CORRECTIVE ASSIGNMENT TO CORRECT THE RECEIVING PARTY DATA ON THE PATENT ASSIGNMENT COVER SHEET PREVIOUSLY RECORDED ON REEL 031582 FRAME 0141. ASSIGNOR(S) HEREBY CONFIRMS THE CONVEYING PARTY IS MEDAREX, INC. AND RECEIVING PARTY IS MEDAREX, L.L.C.. Recorded Nov 13, 2013
From: MEDAREX, INC.
To: MEDAREX, L.L.C.
Reel/Frame 031628/0318 →
MERGER Recorded Nov 12, 2013
From: MEDAREX, INC.
To: PAUL D. GOLIAN / MEDAREX, L.L.C.
Reel/Frame 031582/0141 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 29, 2009
From: AMBROSINO, DONNA; BABCOCK, GREGORY J.; BROERING, TERESA; HERNANDEZ, HECTOR JAVIER; MANDELL, ROBERT; MOLRINE, DEBORAH; THOMAS, WILLIAM D., JR.; GRAZIANO, ROBERT; LOWY, ISRAEL; ZHANG, HUI-FEN
To: MASSACHUSETTS, UNIVERSITY OF; MEDAREX, INC.
Reel/Frame 023297/0078 →
Continuity (4)
Division 11051453 · Feb 4, 2005
Provisional Application 60542357 · Feb 6, 2004
Provisional Application 60613854 · Sep 28, 2004
Related Publication 20100233182A1 · Sep 16, 2010