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Last Updated: April 26, 2024

Claims for Patent: 8,591,888


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Summary for Patent: 8,591,888
Title:Cadherin-11 EC1 domain antagonists for treating inflammatory joint disorders
Abstract: The present invention relates to Cadherin-11 antagonists and compositions comprising Cadherin-11 antagonists. The invention also relates to methods for treating inflammatory joint disorders, such as rheumaotid arthritis, in a mammalian subject by administering a therapeutically effective amount of a Cadherin-11 antagonist.
Inventor(s): McArthur; James G. (Concord, MA)
Assignee: Synovex Corporation (Medford, MA)
Application Number:12/811,921
Patent Claims:1. A method of inhibiting the development of or reducing the severity of an inflammatory joint disorder in a mammalian subject in need thereof, comprising administering to the subject a therapeutically effective amount of an isolated antibody that specifically binds an EC1 domain of a mammalian Cadherin-11 protein, wherein the antibody binds an epitope comprising SEQ ID NO:11 in the EC1 domain of the mammalian Cadherin-11 protein, thereby inhibiting the development of or reducing the severity of the inflammatory joint disorder in the subject.

2. The method of claim 1, wherein the inflammatory joint disorder is selected from the group consisting of rheumatoid arthritis, osteoarthritis, psoriatic arthritis, Reiter's syndrome and ankylosing spondylitis.

3. The method of claim 1, wherein the inflammatory joint disorder is rheumatoid arthritis.

4. The method of claim 1, wherein the mammalian subject is a human.

5. The method of claim 1, wherein the isolated antibody inhibits migration, adhesion, invasion into cartilage, or intercellular signaling of cells that express said mammalian Cadherin-11 protein in one or more joints of said subject.

6. The method of claim 1, wherein the isolated antibody inhibits induction of expression or activity of an enzyme selected from the group consisting of a collagenase, a serine protease, and a matrix metalloproteinase in cells that express said mammalian Cadherin-11 protein in one or more joints of said subject.

7. The method of claim 1, wherein the isolated antibody inhibits induction of expression or activity of a cytokine or growth factor selected from the group consisting of a IL-6, IL-8, RANKL and TRANCE in cells that express said mammalian Cadherin-11 protein in one or more joints of said subject.

8. The method of claim 1, wherein isolated antibody is administered in combination with a disease-modifying anti-rheumatic drug.

9. The method of claim 1, wherein the isolated antibody binds SEQ ID NO:3.

10. The method of claim 1, wherein the isolated antibody is administered systemically.

11. The method of claim 1, wherein the isolated antibody is administered intravenously.

12. The method of claim 1, wherein the isolated antibody is administered by direct injection into a joint.

13. The method of claim 8, wherein the disease-modifying anti-rheumatic drug is methotrexate.

14. The method of claim 1, wherein the isolated antibody is administered in combination with an anti-inflammatory agent.

15. The method of claim 14, wherein the anti-inflammatory agent is an NSAID selected from the group consisting of detoprofen, diclofenac, diflunisal, etodolac, fenoprofen, flurbiprofen, ibuprofen, indomethacin, ketoprofen, meclofenameate, mefenamic acid, meloxicam, nabumeone, naproxen sodium, oxaprozin, piroxicam, sulindac, tolmetin, celecoxib, rofecoxib, aspirin, choline salicylate, salsalte, and sodium and magnesium salicylate.

16. The method of claim 14, wherein the anti-inflammatory agent is a disease modifying antirheumatic drug selected from the group consisting of cyclosporine, azathioprine, methotrexate, leflunomide, cyclophosphamide, hydroxychloroquine, sulfasalazine, D-penicillamine, minocycline, and gold.

17. The method of claim 14, wherein the anti-inflammatory agent is a steroid selected from the group consisting of cortisone, dexamethasone, hydrocortisone, methylprednisolone, prednisolone, prednisone, and triamcinolone.

18. The method of claim 14, wherein the anti-inflammatory agent is a recombinant protein selected from the group consisting of etanercept, infliximab, abatabacept, tocilizumab, and rituximab.

19. The method of claim 1, wherein the isolated antibody is administered to the subject in a dose of about 0.3 mg/kg to about 30 mg/kg body weight per treatment.

20. The method of claim 1, wherein the isolated antibody inhibits cartilage erosion in one or more joints of said subject.

21. A method of inhibiting the development of or reducing the severity of rheumatoid arthritis in a human subject in need thereof, comprising administering to the subject a therapeutically effective amount of an isolated antibody that specifically binds an EC1 domain of a human Cadherin-11 protein, wherein the antibody binds an epitope comprising SEQ ID NO:11 in the EC1 domain of the mammalian Cadherin-11 protein, thereby inhibiting the development of or reducing the severity of the rheumatoid arthritis in the subject.

22. The method of claim 21, wherein the isolated antibody is a humanized antibody.

23. The method of claim 21, wherein the isolated antibody inhibits cartilage erosion in one or more joints of said subject.

Details for Patent 8,591,888

Applicant Tradename Biologic Ingredient Dosage Form BLA Approval Date Patent No. Expiredate
Smith & Nephew, Inc. SANTYL collagenase Ointment 101995 06/04/1965 ⤷  Try a Trial 2028-01-11
Genentech, Inc. RITUXAN rituximab Injection 103705 11/26/1997 ⤷  Try a Trial 2028-01-11
Idec Pharmaceuticals Corp. RITUXAN rituximab Injection 103737 02/19/2002 ⤷  Try a Trial 2028-01-11
Janssen Biotech, Inc. REMICADE infliximab For Injection 103772 08/24/1998 ⤷  Try a Trial 2028-01-11
Immunex Corporation ENBREL etanercept For Injection 103795 11/02/1998 ⤷  Try a Trial 2028-01-11
Immunex Corporation ENBREL etanercept For Injection 103795 05/27/1999 ⤷  Try a Trial 2028-01-11
Immunex Corporation ENBREL etanercept Injection 103795 09/27/2004 ⤷  Try a Trial 2028-01-11
>Applicant >Tradename >Biologic Ingredient >Dosage Form >BLA >Approval Date >Patent No. >Expiredate

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