Methods of administering anti-TNFα antibodies
Methods of treating disorders in which TNFα activity is detrimental via biweekly, subcutaneous administration of human antibodies, preferably recombinant human antibodies, that specifically bind to human tumor necrosis factor α (hTNFα) are disclosed. The antibody may be administered with or without methotrexate. These antibodies have high affinity for hTNFα (e.g., K d =10 −8 M or less), a slow off rate for hTNFα dissociation (e.g., K off =10 −3 sec −1 or less) and neutralize hTNFα activity in vitro and in vivo. An antibody of the invention can be a full-length antibody or an antigen-binding portion thereof. Kits containing a pharmaceutical composition and instructions for dosing, and preloaded syringes containing pharmaceutical compositions are also encompassed by the invention.
1. A method for treating rheumatoid arthritis in a human subject, comprising administering subcutaneously to a human subject having rheumatoid arthritis a total body dose of 40 mg of a human anti-TNFα antibody once every 13-15 days for a time period sufficient to treat the rheumatoid arthritis, wherein the anti-TNFα antibody comprises: an IgG1 heavy chain constant region; a variable light (“VL”) chain region comprising a CDR1 having the amino acid sequence of SEQ ID NO:7, a CDR2 having the amino acid sequence of SEQ ID NO:5, and a CDR3 having the amino acid sequence of SEQ ID NO:3; and a variable heavy (“VH”) chain region comprising a CDR1 having the amino acid sequence of SEQ ID NO:8, a CDR2 having the amino acid sequence of SEQ ID NO:6 and a CDR3 having the amino acid sequence of SEQ ID NO:4, wherein the human subject achieves an ACR20.
2. The method of claim 1 , wherein the V L chain region of the anti-TNFα antibody has the amino acid sequence of SEQ ID NO:1 and the VH chain region of the anti-TNFα antibody has the amino acid sequence of SEQ ID NO:2.
3. The method of claim 1 , wherein the anti-TNFα antibody is administered for a period of at least 24 weeks.
4. The method of claim 2 , wherein the anti-TNFα antibody is administered for a period of at least 24 weeks.
5. The method of claim 1 , wherein the anti-TNFα antibody is administered in combination with methotrexate.
6. The method of claim 2 , wherein the anti-TNFα antibody is administered in combination with methotrexate.
7. The method of claim 3 , wherein the anti-TNFα antibody is administered in combination with methotrexate.
8. The method of claim 4 , wherein the anti-TNFα antibody is administered in combination with methotrexate.
9. A method for treating rheumatoid arthritis in a human subject, comprising administering subcutaneously to a human subject having rheumatoid arthritis a total body dose of 40 mg of a human anti-TNFα antibody once every 13-15 days for a time period sufficient to treat the rheumatoid arthritis, wherein the anti-TNFα antibody comprises: an IgG1 heavy chain constant region; a variable light (“VL”) chain region comprising a CDR1 having the amino acid sequence of SEQ ID NO:7, a CDR2 having the amino acid sequence of SEQ ID NO:5, and a CDR3 having the amino acid sequence of SEQ ID NO:3; and a variable heavy (“VH”) chain region comprising a CDR1 having the amino acid sequence of SEQ ID NO:8, a CDR2 having the amino acid sequence of SEQ ID NO:6 and a CDR3 having the amino acid sequence of SEQ ID NO:4, wherein the human subject achieves an ACR50.
10. The method of claim 9 , wherein the V L chain region of the anti-TNFα antibody has the amino acid sequence of SEQ ID NO:1 and the V H chain region of the anti-TNFα antibody has the amino acid sequence of SEQ ID NO:2.
11. The method of claim 9 , wherein the anti-TNFα antibody is administered for a period of at least 24 weeks.
12. The method of claim 10 , wherein the anti-TNFα antibody is administered for a period of at least 24 weeks.
13. The method of claim 9 , wherein the anti-TNFα antibody is administered in combination with methotrexate.
14. The method of claim 10 , wherein the anti-TNFα antibody is administered in combination with methotrexate.
15. The method of claim 11 , wherein the anti-TNFα antibody is administered in combination with methotrexate.
16. The method of claim 12 , wherein the anti-TNFα antibody is administered in combination with methotrexate.
17. A method for treating rheumatoid arthritis in a human subject, comprising administering subcutaneously to a human subject having rheumatoid arthritis a total body dose of 40 mg of a human anti-TNFα antibody once every 13-15 days for a time period sufficient to treat the rheumatoid arthritis, wherein the anti-TNFα antibody comprises: an IgG1 heavy chain constant region; a variable light (“VL”) chain region comprising a CDR1 having the amino acid sequence of SEQ ID NO:7, a CDR2 having the amino acid sequence of SEQ ID NO:5, and a CDR3 having the amino acid sequence of SEQ ID NO:3; and a variable heavy (“VH”) chain region comprising a CDR1 having the amino acid sequence of SEQ ID NO:8, a CDR2 having the amino acid sequence of SEQ ID NO:6 and a CDR3 having the amino acid sequence of SEQ ID NO:4, wherein the human subject achieves an ACR70.
18. The method of claim 17 , wherein the V L chain region of the anti-TNFα antibody has the amino acid sequence of SEQ ID NO:1 and the V H chain region of the anti-TNFα antibody has the amino acid sequence of SEQ ID NO:2.
19. The method of claim 17 , wherein the anti-TNFα antibody is administered for a period of at least 24 weeks.
20. The method of claim 18 , wherein the anti-TNFα antibody is administered for a period of at least 24 weeks.
21. The method of claim 17 , wherein the anti-TNFα antibody is administered in combination with methotrexate.
22. The method of claim 18 , wherein the anti-TNFα antibody is administered in combination with methotrexate.
23. The method of claim 19 , wherein the anti-TNFα antibody is administered in combination with methotrexate.
24. The method of claim 20 , wherein the anti-TNFα antibody is administered in combination with methotrexate.