US2023279093A1PendingUtilityA1

Methods of Treatment Using Anti-IL-17A/F Antibodies

Assignee: UCB Biopharma SRLPriority: Oct 27, 2015Filed: Oct 11, 2022Published: Sep 7, 2023
Est. expiryOct 27, 2035(~9.2 yrs left)· nominal 20-yr term from priority
C07K 2317/33A61K 2039/505A61K 2039/54C07K 2317/24A61K 2039/545C07K 2317/76C07K 2317/92A61P 17/06A61P 19/02C07K 16/244C07K 2317/56C07K 2317/34A61K 2039/55A61K 39/395
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Claims

Abstract

The invention relates to therapeutic uses of antibody molecules having specificity for antigenic determinants of both IL-17A and IL-17F in the treatment of dermatological and rheumatological diseases, such as psoriasis, psoriatic arthritis and axial spondyloarthritis.

Claims

exact text as granted — not AI-modified
1 .- 25 . (canceled) 
     
     
         26 . A method of reducing psoriasis in a human comprising the step of administering to the human a neutralizing antibody which binds human IL-17A and human IL-17F. 
     
     
         27 . The method of  claim 26 , wherein the psoriasis is plaque psoriasis. 
     
     
         28 . The method of  claim 26 , wherein the reduction of plaque psoriasis is measured by PASI criteria. 
     
     
         29 . The method of  claim 26 , comprising administering an amount of antibody that achieves at least a 75% or 90% change in lesion severity score (LSS) compared to pre-treatment at four, six, or eight weeks following administration of the antibody. 
     
     
         30 . The method of  claim 26 , comprising administering an amount of antibody that achieves at least a 75% or 90% change in Psoriasis Area and Severity Index (PASI) compared to pre-treatment at four, six, or eight weeks following administration of the antibody. 
     
     
         31 .- 83 . (canceled) 
     
     
         84 . The method of treating psoriasis of any one of  claims 26 - 30  and  33 - 35 , wherein the method comprises administering (a) 64 mg of antibody every four weeks, (b) 160 mg of antibody every four weeks or every 8 weeks, (c) 320 mg of antibody every four weeks or every eight weeks, (d) 320 mg loading dose of antibody followed by a maintenance dose of 160 mg of antibody every four weeks, or (e) 480 mg of antibody every four weeks. 
     
     
         85 .- 88 . (canceled) 
     
     
         89 . A method of treating psoriatic arthritis, psoriasis, rheumatoid arthritis or ankylosing spondylitis in a human, comprising the step of administering to the human a loading dose of a neutralizing antibody which binds human IL-17A and human IL-17F followed by at least one maintenance dose of the antibody. 
     
     
         90 .- 124 . (canceled)

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