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Terminated Phase 2 Interventional Results available

ATI-502 Topical Solution for the Treatment of Alopecia Areata (AA), Alopecia Universalis (AU) and Alopecia Totalis (AT)

ClinicalTrials.gov ID: NCT03759340

Public ClinicalTrials.gov record NCT03759340. 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 21, 2026, 12:04 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

Open-Label Study of ATI-502 Topical Solution for the Treatment of Alopecia Areata (AA), Alopecia Universalis (AU) and Alopecia Totalis (AT)

Brief summary

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

This is an open label study of ATI-502 Topical Solution for the treatment of AA, AU, and AT with the following goals: * To assess the safety, tolerability, and efficacy of ATI-502 Topical Solution in subjects with AA, AU or AT following 24 weeks of treatment with ATI-501 Oral Suspension or Placebo Suspension. * To assess the ability of ATI-502 Topical Solution to maintain or improve hair regrowth in subjects previously treated with ATI-501 Oral Suspension or Placebo Suspension.

Study identification

NCT ID
NCT03759340
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 2
Lead sponsor
Aclaris Therapeutics, Inc.
Industry
Enrollment
56 participants

Conditions and interventions

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
Jan 15, 2019 (Actual)
Primary completion
Sep 11, 2019 (Actual)
Completion
Sep 11, 2019 (Actual)
Last update posted
Oct 6, 2020

2019

United States locations

U.S. sites
20
U.S. states
15
U.S. cities
20
Facility City State ZIP Site status
Aclaris Investigator Site Rogers Arkansas 72758 —
Aclaris Investigator Site Denver Colorado 80210 —
Aclaris Investigator Site Boynton Beach Florida 33472 —
Aclaris Investigator Site Snellville Georgia 30078 —
Aclaris Investigator Site Clinton Township Michigan 48038 —
Aclaris Investigator SIte Detroit Michigan 48202 —
Aclaris Investigator Site Fridley Minnesota 55432 —
Aclaris Investigator Site Minneapolis Minnesota 55455 —
Aclaris Investigator Site Saint Joseph Missouri 64506 —
Aclaris Investigator Site Omaha Nebraska 68144 —
Aclaris Investigator Site Las Vegas Nevada 89148 —
Aclaris Investigator Site New York New York 10075 —
Aclaris Investigator Site Rochester New York 14623 —
Aclaris Investigator Site Portland Oregon 97223 —
Aclaris Investigator Site Greenville South Carolina 29607 —
Aclaris Investigator Site Knoxville Tennessee 37922 —
Aclaris Investigational Site Nashville Tennessee 37215 —
Aclaris Investigational Site Austin Texas 78745 —
Aclaris Investigator Site Houston Texas 77056 —
Aclaris Investigator Site Lynchburg Virginia 24501 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT03759340, 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 Oct 6, 2020 · Synced Oct 21, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT03759340 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →