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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 Sep 2, 2026, 11:46 AM 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 19, 2024
Primary completion
Sep 22, 2025
Completion
Dec 17, 2025
Last update posted
Aug 9, 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 9, 2026 · Synced Sep 2, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT06588738 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →