A Real-world Observational Study to Compare Effectiveness of Deucravacitinib Vs Apremilast in Adults With Plaque Psoriasis
Part of paid clinical trials in Waltham, Massachusetts.
- Sponsor
- Bristol-Myers Squibb
- Study ID
- NCT05744466
- Status
- Recruiting
Conditions
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- Deucravacitinib — DRUGAs prescribed by treating clinician
- Apremilast — DRUGAs prescribed by treating clinician
Study Details
The purpose of this study is to understand the comparative effectiveness of deucravacitinib versus apremilast in adults with plaque psoriasis.
Key Dates
- Start date
- Sep 30, 2022
- Status verified
- Jul 2024
- Primary completion
- Dec 10, 2027
- Completion
- Dec 10, 2027
Study Design
- Enrollment
- 1,500 participants (estimated)
Arms
- Arm: Cohort 1Participants that have initiated deucravacitinib
- Arm: Cohort 2Participants that have initiated apremilast
Primary Outcome Measure
Change in body surface area (BSA) [ Time Frame: At baseline and every 6 months up to 60 months or treatment discontinuation ]
Central Contacts
- BMS Study Connect Contact Center www.BMSStudyConnect.com855-907-3286
- First line of the email MUST contain the NCT# and Site #.
Locations (1)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| Local Institution | Waltham | Massachusetts | 02451 | - |
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