Effectiveness and Safety of BMS-986165 Compared to Placebo and Active Comparator in Participants With Psoriasis
Part of paid clinical trials in Birmingham, Alabama.
- Sponsor
- Bristol-Myers Squibb
- Study ID
- NCT03624127
- Phase
- PHASE3
- Status
- Completed
Conditions
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- BMS-986165 — DRUGSpecified dose on specified days
- Placebo — OTHERSpecified dose on specified days
- Apremilast — DRUGSpecified dose on specified days
Study Details
The purpose of this study is to investigate the experimental medication BMS-986165 compared to placebo and a currently available treatment in participants with moderate to severe plaque psoriasis.
Key Dates
- First listed
- Aug 9, 2018
- Start date
- Aug 7, 2018
- Status verified
- Jan 2023
- Primary completion
- Sep 2, 2020
- Completion
- Sep 2, 2020
Study Design
- Enrollment
- 666 participants (actual)
- Allocation
- RANDOMIZED
- Intervention model
- PARALLEL
- Primary purpose
- TREATMENT
Arms
- Experimental: BMS-986165
- Placebo Comparator: Placebo
- Active Comparator: Apremilast
Primary Outcome Measure
The Number of Participants With a Static Physician's Global Assessment (sPGA) Score of 0 or 1 in Participants Receiving BMS-986165 Compared to Placebo at Week 16 (sPGA 0/1) [ Time Frame: Week 16 ]
Locations (67)
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