A Real-world Study to Evaluate the Effectiveness of Deucravacitinib in Adults With Plaque Psoriasis in France (RePhlect)
- Sponsor
- Bristol-Myers Squibb
- Study ID
- NCT06701513
- Status
- Recruiting
Conditions
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- Deucravacitinib — DRUGAs prescribed by treating clinician
Study Details
The purpose of this study is to assess the real-world effectiveness of deucravacitinib treatment in adults diagnosed with moderate-to-severe plaque psoriasis
Key Dates
- Start date
- Jan 29, 2025
- Status verified
- May 2026
- Primary completion
- Apr 30, 2028
- Completion
- Apr 30, 2028
Study Design
- Enrollment
- 350 participants (estimated)
Arms
- Arm: Participants that have initiated deucravacitinib treatment
Primary Outcome Measure
Physician's Global Assessment (PGA) 0/1 response [ Time Frame: Baseline and at months 4, 12, 18 (optional), and 24 ]
Central Contacts
- BMS Clinical Trials Contact Center www.BMSClinicalTrials.com855-907-3286
- First line of the email MUST contain NCT # and Site #.
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