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Completed Phase 2 Interventional Results available

ATI-450 vs Placebo in Participants With Moderate to Severe Hidradenitis Suppurativa (HS)

ClinicalTrials.gov ID: NCT05216224

Public ClinicalTrials.gov record NCT05216224. 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 23, 2026, 10:44 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 Phase 2a, Randomized, Double-blind, Placebo-controlled Study to Investigate the Efficacy, Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of ATI-450 vs Placebo in Patients With Moderate to Severe Hidradenitis Suppurativa (HS)

Study identification

NCT ID
NCT05216224
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Aclaris Therapeutics, Inc.
Industry
Enrollment
95 participants

Conditions and interventions

Interventions

  • ATI-450 Drug
  • Placebo oral tablet Drug

Drug

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
Dec 28, 2021
Primary completion
Dec 22, 2022
Completion
Jan 23, 2023
Last update posted
Jan 6, 2026

2021 – 2023

United States locations

U.S. sites
20
U.S. states
13
U.S. cities
20
Facility City State ZIP Site status
Aclaris Investigational Site Birmingham Alabama 35244
Aclaris Investigational Site Fort Smith Arkansas 72916
Aclaris Investigational Site Encino California 91436
Aclaris Investigational Site San Francisco California 94115
Aclaris Investigational Site Thousand Oaks California 91436
Aclaris Investigational Site Boca Raton Florida 33486
Aclaris Investigational Site Hollywood Florida 33021
Aclaris Investigational Site Tampa Florida 33613
Aclaris Investigational Site Marietta Georgia 30060
Aclaris Investigational Site Sandy Springs Georgia 30328
Aclaris Investigational Site Metairie Louisiana 70006
Aclaris Investigational Site Fort Gratiot Michigan 48059
Aclaris Investigational Site Charlotte North Carolina 28277
Aclaris Investigational Site Athens Ohio 45701
Aclaris Investigational Site Mason Ohio 45040
Aclaris Investigational Site Hershey Pennsylvania 17033
Aclaris Investigational Site Anderson South Carolina 29621
Aclaris Investigational Site Nashville Tennessee 37215
Aclaris Investigational Site Houston Texas 77054
Aclaris Investigational Site Sugar Land Texas 77478

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 NCT05216224, 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 Jan 6, 2026 · Synced Jul 23, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT05216224 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →