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Completed Phase 1 Interventional

A Study to Evaluate the Pharmacokinetics, Safety and Tolerability of Upadacitinib in Pediatric Participants With Severe Atopic Dermatitis

ClinicalTrials.gov ID: NCT03646604

Public ClinicalTrials.gov record NCT03646604. 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

An Open-label Multiple Dose Study to Evaluate the Pharmacokinetics, Safety and Tolerability of Upadacitinib in Pediatric Subjects With Severe Atopic Dermatitis

Study identification

NCT ID
NCT03646604
Recruitment status
Completed
Study type
Interventional
Phase
Phase 1
Lead sponsor
AbbVie
Industry
Enrollment
35 participants

Conditions and interventions

Interventions

  • Upadacitinib (ABT-494) Drug

Drug

Eligibility (public fields only)

Age range
2 Years to 12 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
Jan 30, 2019
Primary completion
Aug 28, 2024
Completion
Aug 28, 2024
Last update posted
Feb 9, 2025

2019 – 2024

United States locations

U.S. sites
15
U.S. states
12
U.S. cities
15
Facility City State ZIP Site status
Beach Pediatrics /ID# 207834 Huntington Beach California 92647-6818
Children's Hospital Los Angeles /ID# 206042 Los Angeles California 90027
Pediatric Skin Research, LLC /ID# 213468 Coral Gables Florida 33146-1837
Rybear, Inc /ID# 231801 Fort Lauderdale Florida 33316-1952
IACT Health-Columbus /ID# 216370 Columbus Georgia 31904-8946
Northwestern University Feinberg School of Medicine /ID# 206224 Chicago Illinois 60611-2927
Dawes Fretzin, LLC /ID# 214958 Indianapolis Indiana 46256
Duplicate_Washington University of St. Louis /ID# 206972 St Louis Missouri 63141-6399
University of New Mexico School of Medicine /ID# 206757 Albuquerque New Mexico 87131-0001
Cincinnati Children's Hospital /ID# 207071 Cincinnati Ohio 45229
Oregon Medical Research Center /ID# 206226 Portland Oregon 97239
Penn State University and Milton S. Hershey Medical Center /ID# 207096 Hershey Pennsylvania 17033-2360
Paddington Testing Co., Inc. /ID# 207079 Philadelphia Pennsylvania 19103
Arlington Research Center, Inc /ID# 222901 Arlington Texas 76011
West Virginia University Hospitals /ID# 206792 Morgantown West Virginia 26506

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 3 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT03646604, 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 9, 2025 · Synced May 18, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT03646604 live on ClinicalTrials.gov.

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