A Observational Study to Evaluate Deucravacitinib in Patients With Moderate Plaque Psoriasis in China
- Sponsor
- Bristol-Myers Squibb
- Study ID
- NCT06512337
- Status
- Active Not Recruiting
Conditions
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- Deucravacitinib — DRUGAs per product label
Study Details
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.
Key Dates
- Start date
- Jan 20, 2025
- Status verified
- Apr 2026
- Primary completion
- Mar 11, 2027
- Completion
- Mar 11, 2027
Study Design
- Enrollment
- 153 participants (actual)
Arms
- Arm: Participants treated with deucravacitinibAdults with moderate plaque psoriasis who are newly initiating deucravacitinib according to the product label
Primary Outcome Measure
Number of participants achieving Static Physician's Global Assessment (sPGA) 0/1 score [ Time Frame: Week 16 ]
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