A Study to Evaluate the Efficacy and Safety of ESK-001 in Patients With Moderate to Severe Plaque Psoriasis
Part of paid clinical trials in Phoenix, Arizona.
- Sponsor
- Alumis Inc
- Study ID
- NCT06586112
- Phase
- PHASE3
- Status
- Completed
Conditions
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- Envudeucitinib — DRUGESK-001
- Apremilast — DRUGApremilast
- Placebo — DRUGPlacebo
Study Details
The goal of this clinical trial is to learn if ESK-001 works to treat moderate to severe plaque psoriasis. The main questions it aims to answer are: * Does ESK-001 reduce the severity of people's psoriasis? * How safe is ESK-001 in people with moderate to severe plaque psoriasis? The study includes 2 comparators: a placebo control (a 'dummy' tablet that does not contain the medicine ESK-001 but looks just like it) and an active control (apremilast, which is a medicine approved to treat psoriasis). People taking part in this study must be men or women aged at least 18 years and have had plaque psoriasis for at least 6 months, currently moderate to severe. Participants will: * take drug every day for 24 weeks. * visit the clinic for checkups and tests. * fill out questionnaires about their psoriasis, itch severity, and change in quality of life. * be assessed for health issues and side effects, physical examinations, vital signs, heart electrical activity measurements, and psychological health. * provide blood and urine samples.
Key Dates
- Start date
- Jul 25, 2024
- Status verified
- Apr 2026
- Primary completion
- Sep 19, 2025
- Completion
- Nov 20, 2025
Study Design
- Enrollment
- 912 participants (actual)
- Allocation
- RANDOMIZED
- Intervention model
- PARALLEL
- Primary purpose
- TREATMENT
Arms
- Experimental: ESK-001ESK-001 administered as an oral tablet
- Placebo Comparator: PlaceboMatching oral placebo
- Active Comparator: ApremilastApremilast administered as an oral capsule
Primary Outcome Measure
To determine whether ESK-001 reduces the severity of psoriasis by 75% (using the PASI) or by at least 2 points (using sPGA score) compared to placebo [ Time Frame: 16 weeks ]
Locations (55)
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