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Terminated Phase 2Phase 3 Interventional Results available

A Study to Learn About the Study Medicine Etrasimod in Adults With Moderate to Severe Atopic Dermatitis (AD) Who Have Already Tried Treatments Taken by Mouth or by Injection

ClinicalTrials.gov ID: NCT05732454

Public ClinicalTrials.gov record NCT05732454. 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 22, 2026, 1:12 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 2/3, TWO-PART STUDY TO EVALUATE THE EFFICACY AND LONG-TERM SAFETY WITH ORAL ETRASIMOD, 2 MG, ONCE DAILY IN ADULT PARTICIPANTS WITH MODERATE-TO-SEVERE ATOPIC DERMATITIS WITH A HISTORY OF PRIOR SYSTEMIC TREATMENT FAILURE

Brief summary

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

The purpose of this study is to learn about the safety and effects of the study medicine called etrasimod for the possible treatment of atopic dermatitis (AD), also called eczema, in adults who have already tried AD treatments taken by mouth or by injection that work all over the body. These adults can have moderate to severe AD. This study is seeking participants who: * have AD for at least 1 year * have moderate-to-severe AD * have tried treatments that work all over the body and saw no effects * are willing to apply a moisturizer at least once daily during the study This is a 2-part study that is only selecting about 60 participants for Part 1 as of now. In Part 1, half of the participants will receive etrasimod, a pill to be taken by mouth once daily. The other half will receive a placebo, a pill that looks like etrasimod but has no medicine also taken by mouth once daily. No one will know what treatment the participant is taking. The Sponsor will compare participant experiences of those taking etrasimod to those taking placebo for 16 weeks. This will help determine if the study medicine is safe and effective. After the first 16 weeks, some participants may continue the study knowing they are taking etrasimod for an additional 52 weeks. Those participating for just the first 16-weeks, will need to visit the study clinic at least 6 times during the study (about every 4 weeks), and will have to come for 2 safety follow up visits at 2nd and 4th week after the last dose of study medicine. People who want to and can continue for an additional 52 weeks will need to visit the study clinic for at least 6 more visits making 12 total visits over 68 weeks followed by 2 safety follow up visits at the 2nd and 4th week after the last dose of study medicine. In Part 2 of the study, around 340 more participants will be participating. Everyone will receive etrasimod pills once daily for 52 weeks. Participants will need to go to the study clinic at least 9 times after which they will have to go for 2 more safety follow up visits at the 2nd and 4th weeks after the last dose of study medicine. At every study visit in Part 1 and Part 2, the focus will be on signs and symptoms of AD (like lesions, itch, and pain) as well as general health and overall side effects. Blood samples and vital signs will be taken at every visit. Due to the way the study medicine works, the in-study clinic visit will last at least 4 hours on Day 1 (Part 1 and Part 2) and Week 16 (Part 1).

Study identification

NCT ID
NCT05732454
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 2, Phase 3
Lead sponsor
Pfizer
Industry
Enrollment
58 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years to 80 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
Jan 18, 2023 (Actual)
Primary completion
Apr 29, 2024 (Actual)
Completion
Apr 29, 2024 (Actual)
Last update posted
May 8, 2025

2023 – 2024

United States locations

U.S. sites
44
U.S. states
6
U.S. cities
20
Facility City State ZIP Site status
First OC Dermatology Research Inc Fountain Valley California 92708 —
Jared R. Younger, MD (Ophthalmologist) Fountain Valley California 92708 —
Bryan D. Vo. MD (Pulmonologist) Laguna Hills California 92653 —
California Allergy and Asthma Medical Group Los Angeles California 90025 —
Dr. Carolyn M. Wong Los Angeles California 90025 —
Dr. Gerald Markovitz Los Angeles California 90025 —
Resolution Advanced Imaging Center Santa Monica California 90404 —
Ponce PFT & Medical services, INC [for pulmonology examination] Aventura Florida 33180 —
Advanced Eye Center: Rodrigo Belalcazar, MD Hialeah Florida 33012 —
Direct Helpers Research Center Hialeah Florida 33012 —
Gsi Clinical Research Margate Florida 33063 —
Randy Burks, MD, FACS Margate Florida 33063 —
D & H National Research Centers, Inc. Miami Florida 33155 —
Imaging - Advanced Health Imaging Miami Florida 33155 —
The Selem Center [Ophthalmologist JOSEPH SELEM] Miami Florida 33165 —
Miami Dermatology and Laser Research Miami Florida 33173 —
Ophthalmology - Dr. Edward Boshnick's Global Vision Rehabilitation Center Miami Florida 33173 —
Pulmonology - Miami Pulmonology Specialists Miami Florida 33173 —
Pelletier Jesse MD North Miami Beach Florida 33162 —
Santos Carlos R MD North Miami Beach Florida 33162 —
Tory Sullivan, Md Pa North Miami Beach Florida 33162 —
Gateway Radiology Pinellas Park Florida 33781 —
Hull & Hull Medical Specialists Plantation Florida 33324 —
GCP Research, Global Clinical professionals St. Petersburg Florida 33705 —
St. Anthonys Hospital St. Petersburg Florida 33705 —
USF Health Tampa Florida 33612 —
Lung and Sleep Disorder Center Lathrup Village Michigan 48076 —
Revival Research Institute, LLC Troy Michigan 48084 —
Somerset Opthalmology PC Troy Michigan 48084 —
Eye Institute Tulsa Oklahoma 74136 —
Pulmonary and Sleep Center of Oklahoma Tulsa Oklahoma 74136 —
Vital Prospects Clinical Research Institute, PC Tulsa Oklahoma 74136 —
Monument Health Rapid City Hospital Rapid City South Dakota 57701 —
Health Concepts Rapid City South Dakota 57702 —
In Vision Optical and Eyecare Rapid City South Dakota 57702 —
Eye Care Associates of Arlington Arlington Texas 76010 —
Arlington Research Center Arlington Texas 76011 —
Texas Pulmonary Arlington Texas 76012 —
Alpesh D. Desai, DO PLLC Houston Texas 77008 —
Becky Fredrickson, MD [Optometrist/Ophthalmologist] Houston Texas 77008 —
Rupesh Vakil, MD [Pulmonologist] Houston Texas 77008 —
Acclaim Dermatology Sugar Land Texas 77479 —
Horizon Eye Care and Optical Sugar Land Texas 77479 —
Sweetwater Pulmonary Associates Sugar Land Texas 77479 —

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 30 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT05732454, 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 May 8, 2025 · Synced Oct 22, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT05732454 live on ClinicalTrials.gov.

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