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Active, not recruiting Phase 2 Interventional

ATI-045 Versus Placebo in Patients With Moderate-to-Severe Atopic Dermatitis

ClinicalTrials.gov ID: NCT07011706

Public ClinicalTrials.gov record NCT07011706. 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 16, 2026, 10:11 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 Randomized, Double-Blinded, Placebo-Controlled Study to Evaluate the Efficacy and Safety of ATI-045 in Patients With Moderate-to-Severe Atopic Dermatitis

Brief summary

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

This study evaluates ATI-045 versus placebo in patients with Moderate-to-Severe Atopic Dermatitis.

Study identification

NCT ID
NCT07011706
Recruitment status
Active, not recruiting
Study type
Interventional
Phase
Phase 2
Lead sponsor
Aclaris Therapeutics, Inc.
Industry
Enrollment
110 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years to 70 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
May 30, 2025 (Actual)
Primary completion
Sep 21, 2026 (Actual)
Completion
Nov 24, 2026 (Estimated)
Last update posted
Sep 29, 2026

2025 – 2026

United States locations

U.S. sites
53
U.S. states
20
U.S. cities
50
Facility City State ZIP Site status
Aclaris Clinical Site Phoenix Arizona 85008 —
Aclaris Clinical Site Tucson Arizona 85704 —
Aclaris Study Site Bryant Arkansas 71913 —
Aclaris Clinical Site Beverly Hills California 90212 —
Aclaris Study Site Encinitas California 92024 —
Aclaris Clinical Site Encino California 91436 —
Aclaris Clinical Site Huntington Beach California 92647 —
Aclaris Study Site Los Angeles California 90045 —
Aclaris Study Site Oceanside California 92056 —
Aclaris Study Site Santa Monica California 90404 —
Aclaris Clinical Site Sherman Oaks California 91403 —
Aclaris Clinical Site Thousand Oaks California 91320 —
Aclaris Study Site Coral Gables Florida 33134 —
Aclaris Clinical Site Hollywood Florida 33486 —
Aclaris Clinical Site Jacksonville Florida 32256 —
Aclaris Clinical Site Margate Florida 33063 —
Aclaris Study Site North Miami Beach Florida 33162 —
Aclaris Study Site Sweetwater Florida 33172 —
Aclaris Study Site Tampa Florida 33607 —
Aclaris Clinical Site Wellington Florida 33449 —
Aclaris Clinical Site Atlanta Georgia 30315 —
Aclaris Clinical Site Savannah Georgia 31405 —
Aclaris Study Site Boise Idaho 83706 —
Aclaris Study Site Clarksville Indiana 47129 —
Aclaris Study Site Indianapolis Indiana 46250 —
Aclaris Clinical Site Lafayette Indiana 47906 —
Aclaris Study Site West Lafayette Indiana 47906 —
Aclaris Study Site Bowling Green Kentucky 42104 —
Aclaris Clinical Site Ann Arbor Michigan 48103 —
Aclaris Study Site Auburn Hills Michigan 48326 —
Aclaris Clinical Site Troy Michigan 48084 —
Aclaris Clinical Site Ridgeland Mississippi 39157 —
Aclaris Study Site Saint Joseph Missouri 64506 —
Aclaris Clinical Site Missoula Montana 59804 —
Aclaris Study Site New York New York 10023 —
Aclaris Study Site New York New York 10075 —
Aclaris Clinical Site New York New York 10128 —
Aclaris Clinical Site The Bronx New York 10455 —
Aclaris Clinical Site Cary North Carolina 27518 —
Aclaris Clinical Site Wilmington North Carolina 28405 —
Aclaris Study Site Camp Hill Pennsylvania 17011 —
Aclaris Clinical Site Philadelphia Pennsylvania 19103 —
Aclaris Clinical Site Myrtle Beach South Carolina 29588 —
Aclaris Clinical Site Dallas Texas 75230 —
Aclaris Clinical Site Houston Texas 77004 —
Aclaris Study Site San Antonio Texas 78213 —
Aclaris Study Site San Antonio Texas 78218 —
Aclaris Clinical Site The Woodlands Texas 77380 —
Aclaris Study Site Webster Texas 77598 —
Aclaris Clinical Site Providence Utah 84332 —
Aclaris Study Site Norfolk Virginia 23502 —
Aclaris Clinical Site Seattle Washington 98004 —
Aclaris Clinical Site Spokane Washington 99202 —

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 7 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT07011706, 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 Sep 29, 2026 · Synced Oct 16, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT07011706 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →