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Active, not recruiting Phase 3 Interventional

A Study of Upadacitinib in Adult Participants With Moderate-to-Severe Atopic Dermatitis and Inadequate Response to Dupilumab

ClinicalTrials.gov ID: NCT06389136

Public ClinicalTrials.gov record NCT06389136. 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 Oct 19, 2026, 7:45 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 3b/4 Randomized, Open-label, Efficacy Assessor-Blinded Study, to Evaluate the Efficacy and Safety of Upadacitinib for the Treatment of Adult Subjects With Moderate to Severe Atopic Dermatitis and Inadequate Response to Dupilumab (SWITCH-UP)

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

Atopic dermatitis (AD) is a skin condition that may cause a rash and itching due to inflammation of the skin. Therapies spread over the skin may not be enough to control the AD in trial participants who require systemic anti-inflammatory treatment. This study aims to provide data on the efficacy and safety of upadacitinib at different doses in adult participants with moderate to severe AD. Upadacitinib is an approved drug for the treatment of moderate to severe atopic dermatitis (AD). This study is conducted in 2 periods. During Period 1, participants are randomly assigned into 1 of 2 groups called treatment arms to receive upadacitinib 15mg or dupilumab 300mg. Based on the participants response to upadacitinib 15mg, they may have their dose increased to upadacitinib 30mg after 2 weeks. In Period 2, participants that completed Period 1 will either remain on their assigned dose or be reassigned to a different dose based on their Eczema Area and Severity Index (EASI) response. Approximately 200 adult participants ages 18 to less than 64 with moderate to severe AD who are current users of dupilumab and had a history of inadequate response to dupilumab will be enrolled at up to 130 sites worldwide. The study is comprised of a 35-day Screening Period, an 8-week Open-Label Period 1 and a 24-week Open-Label Period 2 for participants that completed Period 1. Participants will receive upadacitinib oral tablets once daily or dupilumab subcutaneous (SC) injection every other week for 32 weeks and followed for 30 days. There may be higher treatment burden for participants in this trial compared to their standard of care. Participants will attend regular visits during the study at a hospital or clinic. The effect of the treatment will be checked by medical assessments, blood tests, checking for side effects and completing questionnaires.

Study identification

NCT ID
NCT06389136
Recruitment status
Active, not recruiting
Study type
Interventional
Phase
Phase 3
Lead sponsor
AbbVie
Industry
Enrollment
184 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years to 63 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
Jun 14, 2024 (Actual)
Primary completion
Nov 2026 (Estimated)
Completion
May 2027 (Estimated)
Last update posted
Oct 16, 2026

2024 – 2027

United States locations

U.S. sites
84
U.S. states
28
U.S. cities
73
Facility City State ZIP Site status
Cahaba Dermatology and Skin Health Center /ID# 263855 Birmingham Alabama 35244 —
One Of A Kind Clinical Research Center - Scottsdale /ID# 278675 Scottsdale Arizona 85253 —
Clinical Trials Institute - Northwest Arkansas /ID# 267290 Fayetteville Arkansas 72703 —
Exalt Clinical Research /ID# 281611 Chula Vista California 91910 —
Private Practice - Dr. Tooraj Raoof /ID# 263849 Encino California 91436 —
First Oc Dermatology /ID# 263349 Fountain Valley California 92708 —
NorCal Medical Research /ID# 278397 Greenbrae California 94904 —
Allergy & Asthma Associates of Southern California - Mission Viejo /ID# 266574 Mission Viejo California 92691 —
Dermatologist Medical Group of North County- Profound Research /ID# 266512 Oceanside California 92056 —
Comprehensive Dermatology Center of Pasadena /ID# 281014 Pasadena California 91105 —
Stanford University School of Medicine - Redwood City /ID# 263776 Redwood City California 94063 —
West Dermatology La Jolla /ID# 265014 San Diego California 92121 —
Clinical Trials Research Institute /ID# 263846 Thousand Oaks California 91320 —
Yale University School of Medicine /ID# 263836 New Haven Connecticut 06510 —
Clearlyderm Dermatology - West Boca /ID# 264923 Boca Raton Florida 33428 —
Skin Care Research Boca Raton /ID# 263733 Boca Raton Florida 33486-2269 —
Apex Clinical Trials /ID# 263747 Brandon Florida 33511 —
TrueBlue Clinical Research - Brandon /ID# 265037 Brandon Florida 33511 —
Life Clinical Trials - Coral Springs /ID# 267195 Coral Springs Florida 33071 —
Revival Research - Doral /ID# 263541 Doral Florida 33122 —
FXM Clinical Research Ft. Lauderdale /ID# 280911 Fort Lauderdale Florida 33308 —
Skin Care Research - Hollywood /ID# 263739 Hollywood Florida 33021-6748 —
Solutions Through Advanced Research /ID# 263392 Jacksonville Florida 32256 —
GSI Clinical Research /ID# 263760 Margate Florida 33063-7011 —
Research Associates of South Florida /ID# 267291 Miami Florida 33134 —
International Dermatology Research /ID# 264961 Miami Florida 33144 —
FAX Pharma Clinical Research /ID# 280915 Miami Florida 33146 —
Sullivan Dermatology /ID# 263537 Miami Florida 33162 —
Lenus Research and Medical Group /ID# 263779 Miami Florida 33172 —
Quality Research of South Florida /ID# 266496 Miami Lakes Florida 33016 —
Fxm Clinical Research - Miramar /ID# 280934 Miramar Florida 33027 —
Global Clinical Professionals (GCP) /ID# 266474 St. Petersburg Florida 33705 —
Skin Care Research - Tampa /ID# 263750 Tampa Florida 33607-6438 —
Alliance Clinical Research of Tampa /ID# 264531 Tampa Florida 33615 —
Encore Medical Research - Weston /ID# 278491 Weston Florida 33331 —
Centricity Research Columbus Dermatology /ID# 266529 Columbus Georgia 31904 —
Cleaver Medical Group Dermatology /ID# 263788 Dawsonville Georgia 30534 —
Georgia Skin and Cancer Clinic /ID# 267199 Savannah Georgia 31419 —
Treasure Valley Medical Research /ID# 263738 Boise Idaho 83706 —
DeNova Research /ID# 264513 Chicago Illinois 60610 —
Northwestern Medicine - Northwestern Memorial Hospital /ID# 264983 Chicago Illinois 60611 —
Dawes Fretzin /ID# 264534 Indianapolis Indiana 46256 —
Options Research Group /ID# 264564 West Lafayette Indiana 47906 —
Dermatology Specialists Research (DS Research) - Kentucky /ID# 263388 Louisville Kentucky 40241 —
Velocity Clinical Research at The Dermatology Clinic - Baton Rouge /ID# 267169 Baton Rouge Louisiana 70808-4691 —
Boston Specialists /ID# 265810 Boston Massachusetts 02111-1901 —
Beth Israel Deaconess Medical Center /ID# 263703 Boston Massachusetts 02215 —
Beacon Clinical Research /ID# 263843 Quincy Massachusetts 02169 —
Great Lakes Research Group - Bay City /ID# 263535 Bay City Michigan 48706 —
Henry Ford Medical Center - New Center One /ID# 263522 Detroit Michigan 48202-3046 —
Onyx Clinical Research - Flint - South Linden Road /ID# 267773 Flint Michigan 48532 —
MediSearch Clinical Trials /ID# 263579 Saint Joseph Missouri 64506 —
Physician Research Collaboration, LLC /ID# 263583 Lincoln Nebraska 68516 —
Skin Specialists /ID# 263345 Omaha Nebraska 68144 —
Las Vegas Dermatology /ID# 265801 Las Vegas Nevada 89144 —
Skin Cancer and Dermatology Institute - Reno /ID# 263771 Reno Nevada 89509 —
Dartmouth Hitchcock Medical Center - Old Etna Road /ID# 263840 Lebanon New Hampshire 03766 —
Forest Hills Dermatology Group @ Union Turnpike /ID# 263755 Kew Gardens New York 11415 —
Equity Medical /ID# 265814 New York New York 10023-7340 —
Weill Cornell Medicine /ID# 265793 New York New York 10065 —
Piedmont Plastic Surgery and Dermatology - Huntersville /ID# 266545 Huntersville North Carolina 28078-7961 —
Vital Prospects Clinical Research Institute - Tulsa /ID# 263645 Tulsa Oklahoma 74136 —
Oregon Health and Science University /ID# 263736 Portland Oregon 97239 —
Clinical Research of Philadelphia /ID# 264972 Philadelphia Pennsylvania 19114 —
University of Pittsburgh Medical Center /ID# 264526 Pittsburgh Pennsylvania 15213 —
Dermatology Associates of Plymouth Meeting /ID# 267286 Plymouth Meeting Pennsylvania 19462 —
Medical University of South Carolina /ID# 263655 Charleston South Carolina 29425 —
Advanced Dermatology And Cosmetic Surgery - Spartanburg /ID# 267185 Spartanburg South Carolina 29307 —
Health Concepts /ID# 263383 Rapid City South Dakota 57702 —
Arlington Research Center, Inc /ID# 263665 Arlington Texas 76011 —
Orion Clinical Research /ID# 263658 Austin Texas 78759 —
Bellaire Dermatology Associates /ID# 263794 Bellaire Texas 77401 —
Studies in Dermatology /ID# 263335 Cypress Texas 77429 —
Dermatology Treatment and Research Center /ID# 265812 Dallas Texas 75230 —
Modern Research Associates /ID# 263852 Dallas Texas 75231 —
BRCR Global - Katy /ID# 267304 Katy Texas 77450 —
The Dermatology Institute of South Texas /ID# 267332 McAllen Texas 78501 —
Sms Clinical Research /ID# 278676 Mesquite Texas 75149 —
Texas Dermatology Research Center /ID# 264528 Plano Texas 75025 —
Stride Clinical Research /ID# 267331 Sugar Land Texas 77479 —
The Woodlands Dermatology Associates /ID# 266547 The Woodlands Texas 77380 —
Dermatology Associates of Tyler /ID# 264980 Tyler Texas 75703 —
Fred Hutchinson Cancer Center - Seattle - Fairview Avenue North /ID# 264537 Seattle Washington 98109 —
West Virginia Research Institute - Morgantown /ID# 264930 Morgantown West Virginia 26505 —

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 45 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT06389136, 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 Oct 16, 2026 · Synced Oct 19, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT06389136 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →