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

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 deucravacitinib
    Adults 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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