Methods of administering anti-TNFα antibodies
CAFCFirst Claim
1. A method of reducing signs and symptoms in a patient with moderately to severely active rheumatoid arthritis, comprising:
- administering to said patient, in combination with methotrexate, a human anti-TNFα
antibody,wherein the human anti-TNFα
antibody is administered subcutaneously in a total body dose of 40 mg once every 13-15 days, andwherein 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.
2 Assignments
1 Petition
Accused Products
Abstract
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., Kd=10−8 M or less), a slow off rate for hTNFα dissociation (e.g., Koff=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.
86 Citations
4 Claims
-
1. A method of reducing signs and symptoms in a patient with moderately to severely active rheumatoid arthritis, comprising:
-
administering to said patient, in combination with methotrexate, a human anti-TNFα
antibody,wherein the human anti-TNFα
antibody is administered subcutaneously in a total body dose of 40 mg once every 13-15 days, andwherein 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. - View Dependent Claims (2, 3, 4)
-
Specification