RecruitingPhase 4NCT05858645

Correction of Psoriatic T Cell Signatures by Deucravacitinib


Sponsor

University of California, San Francisco

Enrollment

25 participants

Start Date

Oct 1, 2023

Study Type

INTERVENTIONAL

Conditions

Summary

This study aims to assess cutaneous and blood immune cell function of patients with psoriasis before and after initiation of treatment with the Tyrosine kinase 2 (TYK2) blocker, deucravacitinib.


Eligibility

Min Age: 18 YearsMax Age: 75 Years

Plain Language Summary

Simplified for easier understanding

This study examines how deucravacitinib, a newer oral medication for moderate-to-severe psoriasis, restores abnormal immune cell patterns in the skin. Psoriasis involves overactive T cells — a type of immune cell — that drive inflammation. Deucravacitinib works by blocking a specific signaling pathway called TYK2, and researchers want to understand exactly how this reverses the harmful T cell signatures that cause psoriatic plaques. The study is open to adults aged 18 to 75 with moderate-to-severe psoriasis, defined as affecting at least 10% of body surface area, with a PASI score of 12 or higher and a physician's global assessment of 3 or above. People who are pregnant, breastfeeding, immunocompromised, have active serious infections or cancer, or have used systemic immunosuppressants in the past 12 weeks are excluded. Participants will receive deucravacitinib and provide skin biopsy samples at different timepoints for immune profiling. This research is important because it moves beyond simply measuring whether a drug reduces visible symptoms — it digs into the cellular and molecular machinery of the immune response, which could lead to better-targeted treatments and a deeper understanding of why psoriasis develops in the first place.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DRUGdeucravacitinib

Treatment with deucravacitinib, skin biopsy and blood analysis pre- and mid-treatment


Locations(1)

University of California, San Francisco

San Francisco, California, United States

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NCT05858645


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