A Study to Determine the Efficacy and Safety of Deucravacitinib Compared With Placebo in Participants With Active Psoriatic Arthritis (PsA) Who Are Naïve to Biologic Disease-modifying Anti-rheumatic Drugs
Part of paid clinical trials in Gilbert, Arizona.
- Sponsor
- Bristol-Myers Squibb
- Study ID
- NCT04908202
- Phase
- PHASE3
- Status
- Active Not Recruiting
Conditions
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- Deucravacitinib — DRUGSpecified dose on specified days
- Placebo — OTHERSpecified dose on specified days
Study Details
The purpose of this study is to evaluate the efficacy and safety of deucravacitinib versus placebo in participants with active psoriatic arthritis who are naïve to biologic disease-modifying anti-rheumatic drugs. The long term extension period will provide additional long-term efficacy and safety information.
Key Dates
- Start date
- Jul 13, 2021
- Status verified
- Apr 2026
- Primary completion
- Sep 5, 2024
- Completion
- Jun 10, 2027
Study Design
- Enrollment
- 670 participants (actual)
- Allocation
- RANDOMIZED
- Intervention model
- PARALLEL
- Primary purpose
- TREATMENT
Arms
- Experimental: Deucravacitinib
- Placebo Comparator: Placebo
Primary Outcome Measure
Percentage of Participants With ACR 20 Response at Week 16 [ Time Frame: Week 16 ]
Locations (33)
Related coverage on Hipa.ai
- Deucravacitinib Shows Superior ACR 20 Response in Psoriatic ArthritisDeucravacitinib · Oct 24, 2025 · ClinicalTrials.gov
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