US2014200332A1PendingUtilityA1

Low dose methods for treating disorders in which tnf-alpha activity is detrimental

Assignee: KAYMAKCALAN ZEHRAPriority: Oct 24, 2002Filed: Feb 19, 2014Published: Jul 17, 2014
Est. expiryOct 24, 2022(expired)· nominal 20-yr term from priority
A61P 37/02A61P 9/02A61P 3/10A61P 35/04A61P 9/10A61P 37/00A61P 37/06A61P 37/08A61P 43/00A61P 7/00A61P 9/00A61P 35/02A61P 25/00A61P 31/18A61P 31/04A61P 29/00A61P 31/00A61P 27/06A61P 35/00A61P 27/02A61P 3/00A61P 27/00A61P 25/04A61P 33/06A61P 19/04A61P 1/00A61P 13/12A61P 19/06A61P 19/00A61P 17/00A61P 1/04A61P 11/06A61P 1/16A61P 19/08A61P 19/02A61P 11/00A61K 2039/545A61K 38/1793C07K 2317/92C07K 2317/21A61K 2039/505C07K 2317/24C07K 16/241C07K 2317/94C07K 2317/70C07K 2317/76A61K 38/19A61K 39/395Y02A50/30
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Claims

Abstract

A method of treating TNFα disorders is described, wherein the method comprises administering a low dose amount of a TNFα inhibitor.

Claims

exact text as granted — not AI-modified
1 . A human anti-TNFα antibody which is either D2E7, or a human anti-TNFα antibody with equivalent properties to D2E7 which dissociates from human TNFα with a K d  of 1×10 −8  M or less and a keg rate constant of 1×10 −3  s −1  or less, both determined by surface plasmon resonance, and neutralizes human TNFα cytotoxicity in a standard in vitro L929 assay with an IC 50  of 1×10 −7  M or less, for use in the treatment or alleviation of arthritis, wherein the anti-TNFα antibody is to be administered in a low dose of 0.01-0.11 mg/kg, such that the arthritis is treated or alleviated. 
     
     
         2 . The human anti-TNFα antibody according to  claim 1 , for use in the treatment or alleviation of rheumatoid arthritis. 
     
     
         3 . The human anti-TNFα antibody according to  claim 1 , wherein symptoms associated with the arthritis are alleviated. 
     
     
         4 . The human anti-TNFα antibody according to  claim 1 , wherein symptoms selected from the group consisting of bone erosion, cartilage erosion, inflammation, and vascularity are alleviated. 
     
     
         5 . The human anti-TNFα antibody according to  claim 1 , wherein the arthritis is treated by alleviating symptoms selected from the group consisting of joint distortion, swelling, joint deformation, ankylosis on felxion, and severely impaired movement. 
     
     
         6 . The human anti-TNFα antibody according to  claim 1 , wherein the antibody sequesters TNFα into complexes in a subject suffering from said arthritis. 
     
     
         7 . The human anti-TNFα antibody according to  claim 6 , wherein the serum level of TNFα is higher than the serum level of TNFα a subject not suffering from said arthritis. 
     
     
         8 . The human anti-TNFα antibody according to  claim 1 , which is D2E7.

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