发明名称 Methods of administering anti-TNFα antibodies
摘要 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.
申请公布号 US9073987(B2) 申请公布日期 2015.07.07
申请号 US201414292759 申请日期 2014.05.30
申请人 AbbVie Biotechnology Ltd. 发明人 Fischkoff Steven A.;Kempeni Joachim;Weiss Roberta
分类号 A61K39/395;C07K16/24;A61K9/00;A61K39/00 主分类号 A61K39/395
代理机构 Dechert LLP 代理人 Dechert LLP
主权项 1. A method of reducing signs and symptoms in a patient with moderately to severely active rheumatoid arthritis, comprising: administering to said patient a total body dose of 40 mg of a human anti-TNFα antibody, wherein the dose is administered subcutaneously from a 40 mg dosage unit form once every 13-15 days, and 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.
地址 Hamilton BM