US2013004507A1PendingUtilityA1

METHODS OF ADMINISTERING ANTI-TNFalpha ANTIBODIES

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Assignee: ABBOTT BIOTECH LTDPriority: Jun 8, 2001Filed: Jun 22, 2012Published: Jan 3, 2013
Est. expiryJun 8, 2021(expired)· nominal 20-yr term from priority
A61P 43/00A61P 37/02A61P 9/10A61P 3/10A61P 37/00A61P 37/08A61P 37/06A61P 9/00A61P 41/00A61P 7/04A61P 7/00A61P 31/20A61P 31/00A61P 31/04A61P 25/00A61P 3/00A61P 27/02A61P 27/00A61P 31/14A61P 31/12A61P 29/02A61P 29/00A61P 35/00A61P 1/00A61P 19/08A61P 1/04A61P 17/00A61P 13/00A61P 1/16A61P 13/12A61P 19/06A61P 19/10A61P 11/00A61P 19/02A61P 17/02A61P 19/00C07K 2317/52C07K 2317/56A61K 39/3955A61K 31/519C07K 16/241A61K 9/0019A61K 2039/505A61K 39/395A61K 2039/545C07K 2317/76C07K 2317/565A61K 2039/54A61K 2300/00A61K 45/06C07K 2317/21A61K 38/00C07K 16/24A61M 5/28C07K 16/00Y02A50/30A61K 31/00
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Claims

Abstract

Methods of treating disorders in which TFNα 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.

Claims

exact text as granted — not AI-modified
1 . A method for treating a disorder in a human subject in which the disease is treatable with a TNFα antibody, comprising administering a composition to the human subject in need thereof, on a biweekly dosing regimen such that the disorder is treated, said composition containing an anti-TNFα antibody or an antigen binding portion thereof. 
     
     
         2 . A kit containing a formulation comprising:
 a) a pharmaceutical composition comprising an anti-TNFα antibody and a pharmaceutically acceptable carrier; and   b) instructions for biweekly dosing of the pharmaceutical composition for the treatment of a disorder in which an anti-TNFα antibody or a binding portion thereof is effective in treating the disorder.

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