IP Library Granted Patent US 8,273,349
Granted Patent B2
US 8,273,349 · App. 12/974,938 · Granted Sep 25, 2012

Binding member which binds to both lewis-Y and lewis-B haptens, and its use for treating cancer

Assignee: Cephalon Australia Pty Ltd
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Quick Facts
Patent No.
US 8,273,349
App. No.
12/974,938
Granted
Sep 25, 2012
Kind
B2
Abstract

The invention relates to the use of a binding member which binds to Lewis Y and Lewis b haptens in the treatment of tumours and leukaemia. The binding member may be an antibody which binds to Lewis Y and Lewis b haptens and cancer cells and induces cells death.

Claims (19)

1. A method of treatment of a tumor in a patient, wherein the tumor expresses both Lewis y and Lewis b antigens, comprising:

administering to the patient an effective amount of a naked antibody or fragment thereof, in combination with an active agent, wherein the antibody or fragment thereof binds to both Lewis y and Lewis b haptens and does not bind to H blood group antigen wherein the antibody comprises all the complementarity determining regions (CDRs) of the antibody produced by the cell line deposited as ECACC Accession No. 01050118.

2. The method as claimed in claim 1 , wherein the antibody comprises a constant region of human antibody class IgM, IgA, IgG 2 or IgG 3 .

3. The method as claimed in claim 1 , wherein the active agent is a chemotherapeutic agent.

4. The method as claimed in claim 3 , wherein the chemotherapeutic agent is selected from the group consisting of doxorubicin, taxol, 5-fluorouracil (5 FU), leucovorin, irinotecan, mitomycin C, oxaliplatin, raltitrexed, tamoxifen and cisplatin.

5. The method as claimed in claim 1 , wherein the active agent is selected from the group consisting of aspirin, paracetamol, ibuprofen, ketoprofen, morphine and anti-emetics.

6. The method as claimed in claim 1 , wherein the antibody and active agent are administered simultaneously.

7. The method as claimed in claim 1 , wherein the antibody and active agent are administered sequentially.

8. The method of claim 1 , wherein the tumor is selected from the group consisting of colorectal, breast, ovarian, gastric, leukemia, lung, liver, skin, and myeloid cancer.

9. The method of claim 1 , wherein the patient is a mammal.

10. The method of claim 9 , wherein the patient is a human.

11. A method of treating a tumor in a human patient, wherein the tumor expresses both Lewis y and Lewis b antigens, comprising:

administering to the human patient an effective amount of an isolated antibody or fragment thereof comprising all the complementarity determining regions (CDRs) of the antibody produced by the cell line deposited as ECACC Accession No. 01050118, which antibody or fragment thereof specifically binds to both Lewis y and Lewis b haptens and does not bind to H blood group hapten.

12. The method of claim 11 , wherein the isolated antibody is produced by the cell line deposited as ECACC Accession No. 01050118.

13. A method of treating a tumor in a human patient, wherein the tumor expresses both Lewis y and Lewis b antigens, comprising:

administering to the human patient an effective amount of an isolated antibody fragment comprising all the complementarity determining regions (CDRs) produced by a cell line deposited as ECACC Accession No. 01050118, characterized by specifically binding to Lewis y and Lewis b and not binding to Lewis x .

14. The method of claim 13 , wherein the isolated antibody fragment further characterized by not binding to H blood group antigen by thin layer chromatography.

15. A method of treating a tumor in a human patient, wherein the tumor expresses both Lewis y and Lewis b antigens, comprising:

administering to the human patient an effective amount of an isolated antibody fragment comprising all the complementarity determining regions (CDRs) produced by a cell line deposited as ECACC Accession No. 01050118, characterized by specifically binding to Lewis y and Lewis b and not binding to H blood group antigen by thin layer chromatography.

Assignments (6)
CORRECTIVE ASSIGNMENT TO CORRECT THE CORRECTION OF THE ASSIGNEE ADDRESS TO REMOVE "RON KAL" FROM THE ADDRESS PREVIOUSLY RECORDED ON REEL 031485 FRAME 0798. ASSIGNOR(S) HEREBY CONFIRMS THE NAME CHANGE FROM CEPHALON AUSTRALIA PTY LTD TO TEVA PHARMACEUTICALS AUSTRALIA PTY. Recorded Feb 24, 2014
From: CEPHALON AUSTRALIA PTY LTD
To: TEVA PHARMACEUTICALS AUSTRALIA PTY LTD
Reel/Frame 032403/0365 →
CHANGE OF NAME Recorded Oct 24, 2013
From: CEPHALON AUSTRALIA PTY LTD
To: TEVA PHARMACEUTICALS AUSTRALIA PTY LTD
Reel/Frame 031485/0798 →
CHANGE OF NAME Recorded Jun 13, 2011
From: ARANA THERAPEUTICS PTY LTD
To: CEPHALON AUSTRALIA PTY LTD
Reel/Frame 026434/0978 →
CHANGE OF NAME Recorded Jun 13, 2011
From: ARANA THERAPEUTICS LIMITED
To: ARANA THERAPEUTICS PTY LTD
Reel/Frame 026436/0734 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 13, 2011
From: SCANCELL LIMITED
To: ARANA THERAPEUTICS LIMITED
Reel/Frame 026114/0096 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 12, 2011
From: DURRANT, LINDA G.; PARSONS, TINA
To: SCANCELL LIMITED
Reel/Frame 026119/0432 →
Priority Claims (1)
GB 0111628.4 · May 11, 2001 · national
Continuity (4)
Continuation In Part 12505313 · Jul 17, 2009
Continuation 11831125 · Jul 31, 2007
Continuation 10476233
Related Publication 20110150906A1 · Jun 23, 2011