Envudeucitinib
DrugESK-001
NCT Number: NCT06588738
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.
Looking for future studies?
Notify Me18 year and older
All sexes
Interventional
Phase 3
Klinik Hietzing, Vienna, State of Vienna, Austria
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
ESK-001
Placebo
Apremilast
Time frame: 16 weeks
Proportion of patients achieving ≥75% reduction in PASI score. Proportion of patients achieving a score of 0 or 1 on sPGA.
Time frame: 24 weeks
Proportion of patients achieving of ≥90% or 100% reduction in PASI
Time frame: 24 weeks
Proportion of patients achieving of ≥75% reduction in PASI
Time frame: 24 weeks
Proportion of patients achieving a score of 0 or 1 on sPGA
Time frame: 24 weeks
Change from baseline in %BSA
Time frame: 24 weeks
Proportion of patients achieving a score of 0 or 1 on ssPGA
Time frame: 24 weeks
Proportion of patients achieving a score of 0
Time frame: 24 weeks
Proportion of patients achieving a score of 0 or 1
Time frame: 24 weeks
Change from baseline in Pruritus NRS (scale is from 0 (no pain) to 10 (severe pain)).
Time frame: 24 weeks
Incidence of treatment-emergent adverse events (TEAEs) and serious adverse events (SAEs)
Time frame: 24 weeks
Maximum [Cmax] and minimum [Cmin] plasma concentration
Looking for future studies?
Notify MeAlumis Inc
Industry
A Multicenter, Randomized, Double-Blind, Placebo and Active Comparator Controlled Phase 3 Study in Patients With Moderate to Severe Plaque Psoriasis to Evaluate the Efficacy and Safety of ESK-001 (ONWARD2)
Acronym: ONWARD2
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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