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 — DRUG
    ESK-001
  • Apremilast — DRUG
    Apremilast
  • Placebo — DRUG
    Placebo

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-001
    ESK-001 administered as an oral tablet
  • Placebo Comparator: Placebo
    Matching oral placebo
  • Active Comparator: Apremilast
    Apremilast 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)

FacilityCityStateZIPSite coordinators
Alliance DermatologyPhoenixArizona85032-
Scottsdale Clinical TrialsScottsdaleArizona85260-
Northwest Arkansas Clinical Trials Center (NWACTC), PLLCRogersArkansas72758-8600-
Exalt Clinical ResearchChula VistaCalifornia91910-
California Dermatology & Clinical Research InstituteEncinitasCalifornia92024-7700-
First OC Dermatology Research IncFountain ValleyCalifornia92708-
Marvel Clinical Research, LLCHuntington BeachCalifornia92647-
Sunwise Clinical Research, LLCLafayetteCalifornia94549-
Wallace Medical Group IncLos AngelesCalifornia90056-
Northridge Clinical Trials - Elite Clinical NetworkNorthridgeCalifornia91325-
Pasadena Clinical TrialsPasadenaCalifornia91101-
Therapeutics Clinical ResearchSan DiegoCalifornia92123-
Unison Clinical Trials/ Shahram Jacobs MDSherman OaksCalifornia91403-1814-
Olive View - UCLA Education & Research InstituteSylmarCalifornia91342-
California Dermatology Institute - Thousand OaksThousand OaksCalifornia91320-2130-
Clearlyderm Dermatology - West Boca RatonBoca RatonFlorida33428-
Driven Clinical ResearchCoral GablesFlorida33134-
Jacksonville Center for Clinical ResearchJacksonvilleFlorida32216-
Glick Skin Institute - MargateMargateFlorida33063-7011-
San Marcus Research Clinic, Inc - MiamiMiami LakesFlorida33014-
Savin Medical Group LLCMiami LakesFlorida33014-
Oceanic Research GroupNorth Miami BeachFlorida33169-
LENUS ResearchSweetwaterFlorida33172-
Caban Skin InstituteTampaFlorida33607-
ForCare Medical CenterTampaFlorida33613-1244-
Skin Care Physicians of Georgia - Warner RobinsMaconGeorgia31217-
MetroMed Clinical TrialsChicagoIllinois60614-3625-
Arlington DermatologyRolling MeadowsIllinois60008-
NorthShore Medical Group - Dermatology - SkokieSkokieIllinois60077-1049-
Dundee DermatologyWest DundeeIllinois60118-
Dawes Fretzin Clinical Research GroupColumbusIndiana47201-
The South Bend ClinicSouth BendIndiana46617-
Equity Medical - Bowling GreenBowling GreenKentucky42104-
Velocity Clinical Research at The Dermatology Clinic, Baton RougeBaton RougeLouisiana70808-
Tulane University School of MedicineNew OrleansLouisiana70112-
MetroBoston Clinical PartnersBrightonMassachusetts02135-
Cleaver DermatologyKirksvilleMissouri63501-5362-
OptiSkinNew YorkNew York10128-0724-
The Ohio State University Wexner Medical Center (OSUWMC) - OSU Dermatology East - ColumbusGahannaOhio43230-5317-
Dermatologists of Southwestern Ohio, LLCMasonOhio45040-4520-
Unity Clinical Research (UCR)Oklahoma CityOklahoma73118-
Velocity Clinical Research, MedfordMedfordOregon97504-
Oregon Medical Research CenterPortlandOregon97201-
Paddington Testing Company Inc.PhiladelphiaPennsylvania19103-
UPMC Department of DermatologyPittsburghPennsylvania15213-
Health ConceptsRapid CitySouth Dakota57702-9208-
Discover Dermatology, LLC d/b/a Goodlettsville Dermatology ResearchGoodlettsvilleTennessee37072-2301-
Discover Dermatology, LLC d/b/a Cumberland Skin Center for Clinical Research under Objective HealthHermitageTennessee37076-
UT Health Houston Department of DermatologyBellaireTexas77401-
Studies in Dermatology, LLCCypressTexas77429-
Reveal Research InstituteFriscoTexas75033-
Austin Institute for Clinical Research - HoustonHoustonTexas77056-
Center for Clinical Studies - Texas Medical CenterHoustonTexas77004-
University of Utah Health Care - Midvalley Health CenterMurrayUtah84107-
Frontier DermatologyMill CreekWashington98012-

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