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Completed Phase 3 Interventional

A Study in Patients With Moderate to Severe Plaque Psoriasis to Evaluate the Efficacy and Safety of ESK-001

ClinicalTrials.gov ID: NCT06588738

Public ClinicalTrials.gov record NCT06588738. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 17, 2026, 5:19 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

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)

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

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.

Study identification

NCT ID
NCT06588738
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Alumis Inc
Industry
Enrollment
862 participants

Conditions and interventions

Interventions

Drug

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Aug 20, 2024 (Actual)
Primary completion
Sep 23, 2025 (Actual)
Completion
Dec 18, 2025 (Actual)
Last update posted
Aug 10, 2026

2024 – 2025

United States locations

U.S. sites
43
U.S. states
16
U.S. cities
39
Facility City State ZIP Site status
Total Skin and Beauty Dermatology Center, PC Birmingham Alabama 35203 —
Chandler Clinical Trials Chandler Arizona 85224 —
Noble Clinical Research Tucson Arizona 85704 —
Zenith Research Inc. Beverly Hills California 90211-1705 —
Raoof MD Encino California 91436 —
Long Beach Research Institute Long Beach California 90805 —
Dermatology Research Associates Los Angeles California 90045 —
Empire Clinical Research - Pomona Pomona California 91767 —
Integrative Skin Science and Research Sacramento California 95815 —
UC San Diego San Diego California 92122 —
Southern California Clinical Research Santa Ana California 92701 —
Clinical Science Institute Dermatology Institute Santa Monica California 90404 —
FXM Clinical Research Ft. Lauderdale LLC Fort Lauderdale Florida 33308 —
Direct Helpers Research Center (DHRC) Hialeah Florida 33012 —
AppleMed Research Group under WCG Miami Florida 33126 —
FAX Pharma Clinical Research Inc Miami Florida 33146 —
FXM Clinical Research - Miami LLC Miami Florida 33175 —
Las Mercedes Medical Research Miami Florida 33196 —
FXM Clinical Research Miramar LLC Miramar Florida 33027 —
Renstar Medical Research Ocala Florida 34470 —
DS Research of Southern Indiana Clarksville Indiana 47129 —
The Indiana Clinical Trials Center Plainfield Indiana 46168 —
DS Research of Kentucky Louisville Kentucky 40241 —
Michigan Center for Research Company Clarkston Michigan 48346 —
Henry Ford Medical Center - Farmington Road Detroit Michigan 48202 —
Revival Research Institute Troy Michigan 48084 —
Grekin Skin Institute Warren Michigan 48088 —
Associated Skin Care Specialists - Minnesota Clinical Study Center New Brighton Minnesota 55112 —
Schlessinger MD Omaha Nebraska 68144 —
Las Vegas Clinical Trials Las Vegas Nevada 89030 —
NYC Health and Hospitals Elmhurst Elmhurst New York 11373 —
Pioneer Clinical Research NY New York New York 10016 —
Cameron Dermatology New York New York 10023 —
DermResearchCenter of New York Stony Brook New York 11790 —
Asheville Clinical Trials Asheville North Carolina 28803 —
WDC Cosmetic and Research Wilmington North Carolina 28405 —
Optima Research Boardman Boardman Ohio 44512 —
Clinical Partners LLC Johnston Rhode Island 02919 —
Modern Research Associates PLLC Dallas Texas 75231 —
SMS Clinical Research Mesquite Texas 75149 —
Progressive Clinical Research - San Antonio San Antonio Texas 78213 —
Center for Clinical Studies (CCS) - Webster/Clear Lake Location Webster Texas 77598 —
Jordan Valley Dermatology South Jordan Utah 84095 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 81 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT06588738, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Aug 10, 2026 · Synced Oct 17, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT06588738 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →