Clinical Trials in China / NCT06512337
Active, not recruiting
Observational
A Observational Study to Evaluate Deucravacitinib in Patients With Moderate Plaque Psoriasis in China
NCT06512337 · tracked via the Priya Life Science China tracker
Condition(s) studied
Plaque Psoriasis
Study summary
The purpose of this study is to collect and evaluate real-world data on the effectiveness of deucravacitinib treatment in adults with moderate plaque psoriasis in China.
Eligibility
Inclusion Criteria:
* Participant aged 18 years or older
* Physician-reported (dermatologist) diagnosis of moderate plaque psoriasis with Body Surface Area ≥ 3% and \< 10%
* Participant newly initiated deucravacitinib according to the label
* Provided written informed consent to participate in the study
Exclusion Criteria:
* Participating in or planning to participate in an interventional clinical trial
* Concomitant use of other systemic treatments for psoriasis at baseline
* Prior treatment of deucravacitinib
Primary outcome measure(s)
- Number of participants achieving Static Physician's Global Assessment (sPGA) 0/1 score — Week 16
- Participant psoriasis Body Surface Area (BSA) involvement — Week 16
- Number of participants achieving absolute Psoriasis Area and Severity Index (PASI) score ≤ 3 — Week 16
Trial sites (5)
| Facility | City | Region | Status |
|---|---|---|---|
| Local Institution - 0001 | Guangzhou | Guangdong | |
| Local Institution - 0002 | Handan | Hebei | |
| Local Institution - 0005 | Dalian | Liaoning | |
| Local Institution - 0004 | Shanghai | Shanghai Municipality | |
| Local Institution - 0003 | Beijing | China |
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Other trials for the same condition
Official registry record
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT06512337 on ClinicalTrials.gov ↗ ← All trials in China