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Terminated Phase 2 Interventional Results available

A Study to Assess Adverse Events and Disease Activity With Cedirogant (ABBV-157) in Adult Participants With Moderate to Severe Psoriasis

ClinicalTrials.gov ID: NCT05044234

Public ClinicalTrials.gov record NCT05044234. 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 23, 2026, 8:38 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 Phase 2b, Multicenter, Randomized, Double-Blind, Placebo-Controlled, Dose-Ranging Study to Evaluate the Safety and Efficacy of Cedirogant (ABBV-157) in Adult Subjects With Moderate to Severe Psoriasis

Brief summary

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

Psoriasis is a chronic disease characterized by marked inflammation and thickening of the skin that results in thick, scaly skin plaques. This study assessed how safe and effective cedirogant (ABBV-157) was compared to placebo in adult participants with moderate to severe psoriasis. Efficacy and safety-related measurements assessed disease activity in participants with plaque psoriasis. Cedirogant (ABBV-157) is an investigational drug being developed for the treatment of chronic plaque psoriasis. Participants were put into 1 of 4 groups, called treatment arms and each group received a different treatment. There was a 1 in 4 chance that participants were assigned to placebo. Participants received oral daily doses of cedirogant or placebo capsules for 16 weeks. There may have been a higher burden for participants in this study compared to usual standard of care. Participants attended regular visits per routine clinical practice. The effect of the treatment was checked by medical assessments, checking for side effects, and questionnaires.

Study identification

NCT ID
NCT05044234
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 2
Lead sponsor
AbbVie
Industry
Enrollment
156 participants

Conditions and interventions

Conditions

Interventions

Drug

Eligibility (public fields only)

Age range
18 Years to 65 Years
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
Nov 16, 2021 (Actual)
Primary completion
Nov 30, 2022 (Actual)
Completion
Nov 30, 2022 (Actual)
Last update posted
Nov 29, 2023

2021 – 2022

United States locations

U.S. sites
37
U.S. states
22
U.S. cities
34
Facility City State ZIP Site status
UAB Department of Dermatology /ID# 238563 Birmingham Alabama 35233 —
Medical Dermatology Specialist /ID# 238518 Phoenix Arizona 85006-2722 —
Arkansas Research Trials, LLC /ID# 238687 North Little Rock Arkansas 72117 —
Encino Research Center /ID# 245950 Encino California 91436 —
Velocity Clinical Research, Inc. /ID# 239536 North Hollywood California 91606 —
Medderm Associates /ID# 238834 San Diego California 92103 —
Lakes Research, LLC /ID# 238831 Miami Florida 33014 —
Florida International Rsrch cr /ID# 245959 Miami Florida 33173 —
Lenus Research & Medical Group /ID# 238695 Sweetwater Florida 33172 —
Advanced Clinical Research Institute /ID# 238697 Tampa Florida 33607-6429 —
Clinical Research Trials of Florida, Inc. /ID# 238709 Tampa Florida 33607 —
ForCare Clinical Research /ID# 238856 Tampa Florida 33613-1244 —
Cleaver Medical Group Dermatology - Dawsonville /ID# 246327 Dawsonville Georgia 30534-6369 —
Marietta Dermatology Clinical Research /ID# 238679 Marietta Georgia 30060-1047 —
Arlington Dermatology /ID# 238701 Rolling Meadows Illinois 60008 —
Dawes Fretzin, LLC /ID# 238704 Indianapolis Indiana 46256 —
Zel Skin & Laser Specialists - Edina /ID# 238714 Edina Minnesota 55424-1200 —
Skin Specialists, PC /ID# 238514 Omaha Nebraska 68144 —
Forest Hills Dermatology Group /ID# 238708 Kew Gardens New York 11415 —
Buffalo Medical Group /ID# 239068 Williamsville New York 14221 —
Darst Dermatology /ID# 238677 Charlotte North Carolina 28277 —
Wilmington Dermatology Center /ID# 246445 Wilmington North Carolina 28403 —
Univ Hosp Cleveland /ID# 245953 Cleveland Ohio 44106 —
Dermatologists of Southwest Ohio, Inc /ID# 238939 Mason Ohio 45040-4520 —
Oregon Dermatology and Research Center /ID# 238823 Portland Oregon 97210 —
University of Pittsburgh MC /ID# 246170 Pittsburgh Pennsylvania 15260 —
Clinical Partners, LLC /ID# 238620 Johnston Rhode Island 02919 —
Clinical Research Center of the Carolinas /ID# 238827 Charleston South Carolina 29407 —
Health Concepts /ID# 238510 Rapid City South Dakota 57702 —
Tennessee Clinical Research Center /ID# 238682 Nashville Tennessee 37215-2885 —
Arlington Research Center, Inc /ID# 244171 Arlington Texas 76011 —
Orion Clinical Research /ID# 238619 Austin Texas 78759-4100 —
Bellaire Dermatology Associates /ID# 247865 Bellaire Texas 77401 —
Center for Clinical Studies - Houston (Binz) /ID# 243700 Houston Texas 77004-8097 —
Progressive Clinical Research /ID# 238565 San Antonio Texas 78229 —
Dermatology Specialists of Spokane /ID# 238809 Spokane Washington 99202 —
West Virginia Research /ID# 238517 Morgantown West Virginia 26505-0589 —

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 16 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT05044234, 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 Nov 29, 2023 · Synced Oct 23, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT05044234 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →