Compositions and methods for treating rheumatoid arthritis
AssigneesSanofi Biotechnology, Regeneron Pharmaceuticals, Inc.
InventorsDeborah BAUER, Alexander BODDY, Neil GRAHAM, Yong LIN, Janie PARRINO, Rahul PATEL, Janet VAN ADELSBERG, Hubert VAN HOOGSTRATEN
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Abstract
The present invention relates to the use of an anti-IL6 receptor antibody in monotherapy for treating rheumatoid arthritis and for improving the physical function and the quality of life of a subject suffering from rheumatoid arthritis.
Claims25
1-23. (canceled)
A method of improving the physical function of a subject suffering from rheumatoid arthritis comprising administering an antibody, wherein:
- the antibody comprises the heavy chain variable region comprising the sequence SEQ ID NO:1 and the light chain variable region comprising the sequence SEQ ID NO:2,
- the antibody is administered subcutaneously at about 150 mg or about 200 mg once every two weeks to the subject,
- the subject is not administered with any other disease-modifying antirheumatic drug (DMARD) in course of administration with the antibody, and
- the subject was previously ineffectively treated for rheumatoid arthritis by administering at least one DMARD different from the antibody.
A method of improving the health related quality of life of a subject suffering from rheumatoid arthritis comprising administering an antibody, wherein:
- the antibody comprises a heavy chain variable region comprising sequence SEQ ID NO:1 and a light chain variable region comprising sequence SEQ ID NO:2,
- the antibody is administered subcutaneously at about 150 mg or about 200 mg once every two weeks to the subject,
- the subject is not administered with any other disease-modifying antirheumatic drug (DMARD) in course of administration with the antibody, and
- the subject was previously ineffectively treated for rheumatoid arthritis by administering at least one DMARD different from the antibody.
A method of treating rheumatoid arthritis in a subject comprising administering an antibody, wherein:
- the antibody comprises a heavy chain variable region comprising sequence SEQ ID NO:1 and a light chain variable region comprising sequence SEQ ID NO:2,
- the antibody is administered subcutaneously at about 150 mg or about 200 mg once every two weeks to the subject,
- the subject is not administered with any other Disease-Modifying AntiRheumatic Drug (DMARD) in course of administration with the antibody, and
- the subject was previously ineffectively treated for rheumatoid arthritis by administering at least one DMARD different from the antibody.
The method according to claim 42, wherein the DMARD is methotrexate.
(canceled)
Dependencies are inferred from the claim text.