NCT05858645PHASE4Recruiting
Correction of Psoriatic T Cell Signatures by Deucravacitinib
University of California, San Francisco
Start Date
10/1/2023
Completion Date
6/1/2028
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.
Detailed Description
This is a one-arm, open-label study to examine the effect of deucravacitinib on cutaneous and blood immune cells of psoriatic patients. 25 subjects with moderate to severe psoriasis will be enrolled. Biopsy and blood samples will be collected before and during treatment and undergo molecular profiling to assess for deucravacitinib-corrected signatures.
Eligibility Criteria
Age Range: 18 years to 75 years
Inclusion Criteria:
1. 18 years of age or older
2. Patients with moderate-severe psoriasis (BSA \>= 10%, PASI \>=12, static Physician's Global Assessment (sPGA) 3 and above)
Exclusion Criteria:
1. taking systemic immunosuppressives in the last 12 weeks
2. pregnancy
3. severe immunodeficiency (either from genetic or infectious causes).
4. tuberculosis or other active serious infection
5. active systemic malignancy.
6. breast-feeding
7. Presence of a condition or abnormality that in the opinion of the Investigator would compromise the safety of the patient or the quality of the data.
Interventions
DRUG
deucravacitinib
Conditions
Psoriasis Vulgaris
Locations
University of California, San Francisco
San Francisco, California 94115
United States