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Completed Phase 2 Interventional Accepts healthy volunteers Results available

ATI-501 Oral Suspension Compared to Placebo in Subjects With Alopecia Areata, Alopecia Universalis or Alopecia Totalis

ClinicalTrials.gov ID: NCT03594227

Public ClinicalTrials.gov record NCT03594227. 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 21, 2026, 10:08 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-Blind, Placebo-Controlled Multicenter Study to Evaluate the Safety, Tolerability and Efficacy of ATI-501 Oral Suspension Compared to Placebo in Adult Subjects With Alopecia Areata, Alopecia Universalis or Alopecia Totalis

Study identification

NCT ID
NCT03594227
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Aclaris Therapeutics, Inc.
Industry
Enrollment
87 participants

Conditions and interventions

Conditions

Interventions

  • ATI-501 400mg BID (Low dose) Drug
  • ATI-501 600mg BID (Mid dose) Drug
  • ATI-501 800mg BID (High dose) Drug
  • Placebo Drug

Drug

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Accepts healthy volunteers

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Jun 10, 2018
Primary completion
Jun 5, 2019
Completion
Jun 17, 2019
Last update posted
Sep 15, 2020

2018 – 2019

United States locations

U.S. sites
25
U.S. states
15
U.S. cities
25
Facility City State ZIP Site status
Aclaris Investigator Site Hot Springs Arkansas 71913
Aclaris Investigator Site Rogers Arkansas 72758
Aclaris Investigator Site Denver Colorado 80210
Aclaris Investigator Site Boynton Beach Florida 33472
Aclaris Investigator Site Miami Florida 33137
Aclaris Investigator Site Sanford Florida 32771
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 Investigator Site Nashville Tennessee 37215
Aclaris Investigational Site Austin Texas 78745
Aclaris Investigator Site Houston Texas 77056
Aclaris Investigator Site San Antonio Texas 78213
Aclaris Investigator Site Lynchburg Virginia 24501
Aclaris Investigator Site Norfolk Virginia 23502

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 NCT03594227, 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 15, 2020 · Synced Jul 21, 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 protocol, eligibility criteria, and contact information for NCT03594227 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →