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Completed Phase 2 Interventional Results available

A Study of Oral Upadacitinib Tablet Compared to Placebo in Adult Participants With Moderate to Severe Hidradenitis Suppurativa to Assess Change in Disease Symptoms

ClinicalTrials.gov ID: NCT04430855

Public ClinicalTrials.gov record NCT04430855. 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 May 18, 2026, 1:02 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 2, Multicenter, Randomized, Placebo-Controlled, Double-Blind Study to Evaluate Upadacitinib in Adult Subjects With Moderate to Severe Hidradenitis Suppurativa

Study identification

NCT ID
NCT04430855
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
AbbVie
Industry
Enrollment
68 participants

Conditions and interventions

Interventions

  • Placebo Drug
  • Upadacitinib Drug

Drug

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
Jul 13, 2020
Primary completion
Apr 21, 2021
Completion
Jan 24, 2022
Last update posted
Feb 5, 2023

2020 – 2022

United States locations

U.S. sites
18
U.S. states
16
U.S. cities
18
Facility City State ZIP Site status
Medical Dermatology Specialist /ID# 221084 Phoenix Arizona 85006-2722
University of Arkansas for Medical Sciences /ID# 218404 Little Rock Arkansas 72205
Medderm Associates /ID# 218317 San Diego California 92103
Skin Care Research - Boca Raton /ID# 218809 Boca Raton Florida 33486-2269
Lakes Research, LLC /ID# 218854 Miami Florida 33014
ForCare Clinical Research /ID# 218013 Tampa Florida 33613-1244
Northshore University Health System Dermatology Clinical Trials Unit /ID# 218319 Skokie Illinois 60077
Dawes Fretzin, LLC /ID# 218310 Indianapolis Indiana 46256
Beth Israel Deaconess Medical Center /ID# 218306 Boston Massachusetts 02215-5400
Washington University-School of Medicine /ID# 218331 St Louis Missouri 63110
Psoriasis Treatment Center of Central New Jersey /ID# 218330 East Windsor New Jersey 08520
Duke Cancer Center /ID# 218526 Durham North Carolina 27710-3000
University Hospitals Case Medical Center /ID# 218326 Cleveland Ohio 44106
Southside Dermatology /ID# 218321 Tulsa Oklahoma 74132
University of Pittsburgh MC /ID# 218329 Pittsburgh Pennsylvania 15260
Medical University of South Carolina /ID# 218318 Charleston South Carolina 29425
Duplicate_Center for Clinical Studies /ID# 218307 Houston Texas 77004
Dermatology Specialists of Spokane /ID# 218760 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 8 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT04430855, 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 Feb 5, 2023 · Synced May 18, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT04430855 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →