Methods for the treatment of rheumatoid arthritis
View Patent ↗The present invention provides compositions and methods of treating and improving the symptoms of rheumatoid arthritis using an antibody or antigen-binding fragment thereof that specifically binds human interleukin-6 receptor (hIL-6R).
1. A method of treating rheumatoid arthritis in a subject previously ineffectively treated by administering methotrexate and previously ineffectively treated by administering a TNF-α antagonist, the method comprising administering to the subject
(a) a therapeutically effective amount of methotrexate, and
(b) about 150 mg to about 200 mg of an antibody once every two weeks, wherein the antibody comprises a heavy chain variable region comprising the sequence SEQ ID NO:2 and a light chain variable region comprising the sequence SEQ ID NO:3 and the antibody is administered subcutaneously, wherein the subject achieves at least a 20% improvement in the American College of Rheumatology core set disease index (ACR20) after treatment.
2. A method of treating rheumatoid arthritis in a subject previously ineffectively treated by administering methotrexate and previously ineffectively treated by administering a TNF-α antagonist, the method comprising administering to the subject:
(a) a therapeutically effective amount of methotrexate, and
(b) about 150 mg of antibody once every two weeks, wherein the antibody comprises a heavy chain variable region comprising the sequence SEQ ID NO:2 and a light chain variable region comprising the sequence SEQ ID NO:3, and the antibody is administered subcutaneously,
wherein the subject achieves at least a 20% improvement in the American College of Rheumatology core set disease index (ACR20) after treatment.
3. A method of treating rheumatoid arthritis in a subject previously ineffectively treated by administering methotrexate and previously ineffectively treated by administering a TNF-α antagonist, the method comprising administering to the subject:
(a) a therapeutically effective amount of methotrexate, and
(b) about 200 mg of antibody once every two weeks, wherein the antibody comprises a heavy chain variable region comprising the sequence SEQ ID NO:2 and a light chain variable region comprising the sequence SEQ ID NO:3, and the antibody is administered subcutaneously,
wherein the subject achieves at least a 20% improvement in the American College of Rheumatology core set disease index (ACR20) after treatment.
4. The method of any one of claims 1 , 2 , or 3 , wherein the subject achieves at least a 50% improvement in the American College of Rheumatology core set disease index (ACR50) after treatment.
5. The method of claim 4 , wherein the subject achieves at least a 50% improvement in the American College of Rheumatology core set disease index after 12 weeks of treatment.
6. The method of any one of claims 1 , 2 , or 3 , wherein the subject achieves at least a 70% improvement in the American College of Rheumatology core set disease index (ACR70) after treatment.
7. The method of claim 6 , wherein the subject achieves at least a 70% improvement in the American College of Rheumatology core set disease index after 12 weeks of treatment.
8. The method of any one of claims 1 , 2 , or 3 , wherein the subject was treated with the TNF-α antagonist for at least 3 months in the last 2 years.
9. The method of any one of claims 1 , 2 , or 3 , wherein the TNF-α antagonist is a biologic anti-TNF-α.
10. The method of any of claims 1 , 2 , or 3 , wherein the TNF-α antagonist is selected from the group consisting of etanercept, infliximab, adalimumab, golimumab and certolizumab pegol.
11. The method of any one of claims 1 , 2 , or 3 , wherein the antibody is sarilumab.
12. The method of any one of claims 1 , 2 , or 3 , wherein the subject achieves at least a 20% improvement in the American College of Rheumatology core set disease index after 12 weeks of treatment.
13. The method of any one of claim 1 , 2 , or 3 , comprising administering between 6 and 25 mg of methotrexate per week.