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Terminated Phase 2 Interventional Results available

A Study of ATI-50002 Topical Solution for the Treatment of Alopecia Areata

ClinicalTrials.gov ID: NCT03354637

Public ClinicalTrials.gov record NCT03354637. 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 Jul 24, 2026, 8:32 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 Randomized, Double-Blind, Vehicle-Controlled Multicenter Study to Evaluate the Safety, Tolerability and Efficacy of ATI-50002 Topical Solution Administered Twice-Daily for 6 Months in Adolescents and Adult Subjects With Stable Patchy Alopecia Areata With Optional Long-Term Open-Label Extension

Study identification

NCT ID
NCT03354637
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 2
Lead sponsor
Aclaris Therapeutics, Inc.
Industry
Enrollment
129 participants

Conditions and interventions

Interventions

  • ATI-50002 high dose Drug
  • ATI-50002 low dose Drug
  • Placebo Drug

Drug

Eligibility (public fields only)

Age range
12 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
Nov 28, 2017
Primary completion
Apr 17, 2019
Completion
Sep 9, 2019
Last update posted
Jun 4, 2020

2017 – 2019

United States locations

U.S. sites
23
U.S. states
13
U.S. cities
21
Facility City State ZIP Site status
Aclaris Investigator Site Encinitas California 92024
Aclaris Investigator Site Laguna Hills California 92653
Aclaris Investigator Site Redwood City California 94063
Aclaris Investigator Site Washington D.C. District of Columbia 20037
Aclaris Investigator Site Boynton Beach Florida 33472
Aclaris Investigator Site Miami Florida 33136
Aclaris Investigator Site Boston Massachusetts 02115
Aclaris Investigator Site Clinton Township Michigan 48038
Aclaris Investigator Site Warren Michigan 48088
Aclaris Investigator Site Fridley Minnesota 55432
Aclaris Investigator Site Minneapolis Minnesota 55455
Aclaris Investigator Site Omaha Nebraska 68144
Aclaris Investigator Site New York New York 10155
Aclaris Investigator Site Durham North Carolina 27710
Aclaris Investigator Site Winston-Salem North Carolina 27104
Aclaris Investigator Site Portland Oregon 97210
Aclaris Investigator Site Fort Washington Pennsylvania 19034
Aclaris Investigator Site Knoxville Tennessee 37922
Aclaris Investigator Site Nashville Tennessee 37215
Aclaris Investigator Site Austin Texas 78745
Aclaris Investigator Site Austin Texas 78759
Aclaris Investigator Site San Antonio Texas 78229
Aclaris Investigator Site San Antonio Texas 78745

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 NCT03354637, 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 Jun 4, 2020 · Synced Jul 24, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT03354637 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →