The goal of this clinical trial is to investigate the efficacy and safety of Deucravacitinib in patients with moderate-to-severe palmoplantar pustulosis. Approximately 25 subjects will be included in the study and receive Deucravacitinib 6mg per day for four months. This study will begin June 2025 and is expected to last 14 months.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
25
25 subjects with palmoplantar pustulosis will be allocated to receive oral Deucravacitinib 6mg everyday for 16 weeks.
Peking University First Hospital
Beijing, China
Primary efficacy endpoint
The primary efficacy endpoint was percentage change from baseline in Palmoplantar Pustular Area and Severity Index (PPPASI) at W16.
Time frame: From enrollment to the end of treatment at 16 weeks
Effect of Deucravacitinib on overall severity of palmoplantar pustulosis
Mean change in erythema and pustules from Baseline to week 16 will be evaluated by Palmoplantar Pustular Physician's Global Assessment (PPPGA).
Time frame: From enrollment to the end of treatment at 16 weeks
Effect of Deucravacitinib on quality of life: Dermatology Life Quality Index (DLQI)
Mean change in quality of life from Baseline to week 16 will be evaluated by Dermatology Life Quality Index (DLQI)
Time frame: From enrollment to the end of treatment at 16 weeks
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