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A Study to Evaluate Effectiveness and Safety of a TYK2 Inhibitor in Subjects With Moderate to Severe Plaque Psoriasis

A Study to Evaluate Effectiveness and Safety of a TYK2 Inhibitor in Subjects With Moderate to Severe Plaque Psoriasis

Recruiting
18-70 years
All
Phase N/A

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Overview

A Study to evaluate efficacy and safety in subjects with moderate to severe Plaque Psoriasis treated with a TYK2 Inhibitor for 12 weeks

Eligibility

Inclusion Criteria:

  • Male and female, ages 18 to 70 years
  • Body weight \>40 kg, body mass index (BMI) of 18 to 40 kg/m2
  • Clinical diagnosis of plaque psoriasis for ≥6 months before the Baseline visit
  • Women of childbearing potential (WOCBP) and males who are sexucally active must agree to follow instructions for method(s) of contraception.

Exclusion Criteria:

  • Diagnosed with non-plaque psoriasis
  • Previously received tyrosine kinase 2 (TYK2) inhibitors
  • Previously received other psoriasis treatments such as biological agents, immunoregulators, or hormonal drugs within a specific period before administration, and the investigator deems it may affect the immunity of the subjects
  • Has participated in any clinical trials within 30 days or 5 half-lives of the drug before the first administration, or currently undergoing visits for other clinical trials;
  • Has history of chronic disease that may affect the study, or acute or chronic severe infectious diseases, such as a history of active or inadequately treated latent tuberculosis infection, severe bone or joint infections within 6 months before screening, and other acute infectious diseases.
  • Has known or suspected skin or systemic autoimmune diseases other than psoriasis and psoriatic arthritis;
  • Other conditions that the investigator deems unsuitable for participation in this study.

Other protocol defined inclusion/exclusion criteria could apply

Study details
    Plaque Psoriasis
    Moderate to Severe Plaque Psoriasis

NCT07234591

Usynova Pharmaceuticals Ltd.

31 January 2026

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