Actively Recruiting
Immune Cell Study in Psoriasis Skin During Anti-interleukin 23 Therapy Analysis of Immune Cells in Lesions of Moderate-Severe Plaque Psoriasis
Led by Fondazione Policlinico Universitario Agostino Gemelli IRCCS · Updated on 2025-01-24
20
Participants Needed
1
Research Sites
121 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Psoriasis is a chronic immune-related skin condition marked by red, itchy plaques. This research focuses on patients with moderate to severe psoriasis who are receiving treatment with anti-interleukin-23 (IL-23) biologic drugs. Although IL-23 blockers are effective, some patients experience relapses or resistant skin areas. The study aims to identify the specific immune cells producing key signaling proteins called cytokines that contribute to the persistence or return of psoriatic lesions during this treatment. Participants will undergo a skin biopsy procedure where a small sample (6 mm punch biopsy) is taken from the psoriatic skin lesion that is resistant to treatment or has flared during anti-IL-23 therapy. This allows researchers to study the immune cells within the affected skin. The study includes patients who have been treated with anti-IL-23 drugs for at least six months and currently have active resistant or recurring lesions. Throughout the study, which lasts approximately one year, researchers will analyze the immune cells in the skin samples to determine the source of important cytokines involved in the disease's persistence or relapse. Participants will provide informed consent and undergo evaluations to ensure the collection of relevant data. The study is designed to improve understanding of immune activity in psoriasis during anti-IL-23 treatment and may inform future therapeutic strategies.
CONDITIONS
Official Title
Immune Infiltrate Analysis of Psoriasis Skin During Therapy With Anti-interleukin 23 (IL-23)
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Moderate to severe psoriasis with a PASI score greater than 10
- Receiving anti-IL-23 biologic therapy for at least 6 months (for patients under treatment)
- During therapy, having at least one area resistant to treatment or at least one disease flare (for patients under treatment)
- Ability to provide informed consent
You will not qualify if you...
- Unable to provide informed consent
- Complete response to anti-IL-23 therapy with no resistant plaques or disease flare-ups
AI-Screening
AI-Powered Screening
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Trial Site Locations
Total: 1 location
1
Fondazione Policlinico Universitario A. Gemelli IRCCS, UOC Dermatologia
Rome, Lazio, Italy, 00168
Actively Recruiting
Research Team
K
Ketty Peris, Prof
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
2
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