IL-23p19 Antibody Dosing Schedule for Long-Interval Psoriasis Remission

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Solution Overview

Problem

There is a significant unmet need for effective, safe, and affordable biologic treatments for psoriasis, particularly in Chinese patients, as existing IL-23p19 monoclonal antibodies are under-utilized and there is a demand for domestic biological agents with lower treatment costs.

Innovation Solution

A dosing regimen for an IL-23p19 antibody with specific CDR sequences is administered at Weeks 0, 4, and 8, followed by doses every 8 to 20 weeks, preferably every 12 weeks, with a first dose of 200 mg, to improve skin lesions and maintain long-term remission in psoriasis patients.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Reliability

If existing IL-23p19 monoclonal antibodies are used for treatment, then therapeutic efficacy is achieved, but treatment cost is high and accessibility is limited

Engineering Contradiction:
Improvetherapeutic efficacyVSAvoidtreatment cost
Core Design Contradiction:
ReliabilityVSEase of manufacture

Solution Approach 1:

The patent creates a domestic copy/version of existing IL-23p19 monoclonal antibodies by identifying and utilizing homologous protein sequences in Chinese patients. This allows development of a treatment that replicates the therapeutic mechanism of imported biologics while being manufactured locally at lower cost, directly addressing the contradiction between efficacy and affordability

Inventive Principle:
Principle #26Copying

Solution Approach 2:

The patent changes the parameter of antigen target specificity by identifying a homologous protein sequence that is specific to Chinese patients rather than using the exact same target as imported antibodies. This parameter change enables the development of a cost-effective domestic alternative that maintains therapeutic efficacy while improving accessibility for Chinese psoriasis patients

Inventive Principle:
Principle #35Parameter changes

2Reliability

If frequent injections are administered to maintain remission, then therapeutic efficacy is maintained, but patient compliance decreases due to physical and psychological burden

Engineering Contradiction:
Improveremission maintenanceVSAvoidpatient compliance
Core Design Contradiction:
ReliabilityVSEase of operation

Solution Approach 1:

The patent implements a periodic dosing regimen where patients receive initial loading doses followed by maintenance doses at extended intervals (every 8 to 20 weeks). This periodic action pattern maintains therapeutic remission while significantly reducing injection frequency compared to weekly or bi-weekly regimens, thereby improving patient compliance by reducing physical burden and psychological stress associated with frequent injections

Inventive Principle:
Principle #19Periodic action

3Adaptability or versatility

If biologics are made more accessible to Chinese patients, then health equity improves, but demand for affordable domestic alternatives increases

Engineering Contradiction:
ImproveaccessibilityVSAvoiddemand for affordable alternatives
Core Design Contradiction:
Adaptability or versatilityVSEase of manufacture

Solution Approach 1:

The patent develops a cost-effective domestic biologic alternative that can be manufactured at lower cost than imported biologics. By creating an affordable domestic version targeting Chinese patients specifically, the patent makes biologics accessible to a broader population while meeting the demonstrated demand for affordable alternatives, thus improving health equity without requiring expensive imported products

Inventive Principle:
Principle #27Cheap short-living objects (Disposable)

Data Source

PatentEP4703379A1Method for treating psoriasis with recombinant interleukin 23p19 antibody
Publication Date: 2026.03.04 INNOVENT BIOLOGICS (SUZHOU) CO LTD
  • EP4703379A1 patent drawing
  • EP4703379A1 patent drawing
  • EP4703379A1 patent drawing

AI summary

The present invention relates to a method for preventing or treating psoriasis in a subject, comprising administering an IL-23p19 antibody to the subject, wherein a first dose of the IL-23p19 antibody is administered at Weeks 0, 4, and 8, respectively, followed by administration of a second dose of the IL-23p19 antibody every 8 Weeks to 20 weeks; and wherein the first dose is 200 mg, and the second dose is 50 mg to 250 mg, and preferably 100 mg to 200 mg.