US2022313818A1PendingUtilityA1

Use of il-17 antagonists to inhibit the progression of structural damage in psoriatic arthritic patients

Assignee: NOVARTIS AGPriority: Sep 10, 2014Filed: Feb 15, 2022Published: Oct 6, 2022
Est. expirySep 10, 2034(~8.1 yrs left)· nominal 20-yr term from priority
C07K 16/244A61K 2039/545A61K 2039/505A61K 39/3955A61P 29/00A61K 45/00A61P 37/06A61P 43/00A61P 19/08A61P 19/02C07K 16/18A61P 17/06A61K 39/00C07K 2317/92
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Claims

Abstract

The present disclosure relates to methods, uses, medicaments, pharmaceutical formulations, dosage forms, and kits for inhibiting the progression of structural damage in psoriatic arthritis (PsA) patients using IL-17 antagonists, e.g., IL-17 antibodies and antigen-binding fragments thereof, e.g., secukinumab.

Claims

exact text as granted — not AI-modified
1 . A method of inhibiting the progression of structural damage in a PsA patient, comprising selectively administering 75 mg to 300 mg of an IL-17 antagonist to a patient in need thereof by subcutaneous administration, wherein the IL-17 antagonist is secukinumab, and wherein the patient is selected for treatment with the dose of about 75 mg to 300 mg based on the patient previously failing treatment with a Tumor Necrosis Factor (TNF) alpha antagonist or previously responding inadequately to treatment with a TNF alpha antagonist. 
     
     
         2 .- 6 . (canceled) 
     
     
         7 . The method according  claim 1 , wherein inhibition of the progression of structural damage is measured by the van der Heijde psoriatic arthritis-modified total Sharp score (mTSS). 
     
     
         8 .- 10 . (canceled) 
     
     
         11 . The method according  claim 1 , wherein the patient has concomitant psoriasis. 
     
     
         12 . The method according  claim 1 , wherein inhibiting the progression of structural damage is defined as a change from baseline in mTSS≤0.5. 
     
     
         13 - 18 . (canceled) 
     
     
         19 . The method according to  claim 1 , wherein secukinumab is s.c. administered to the patient at about 75 mg, or about 150 mg or about 300 mg weekly during weeks 0, 1, 2, 3, and 4 and thereafter at about 150 mg or about 300 mg every 4 weeks. 
     
     
         20 . The method according claim  17 , wherein secukinumab is s.c. administered to the patient at about 75 mg, or about 150 mg or about 300 mg monthly. 
     
     
         21 .- 28 . (canceled)

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