A Study to Assess Adverse Events and Change in Disease Activity Comparing Oral Upadacitinib to Subcutaneous Dupilumab in Children From 2 to Less Than 12 Years of Age With Moderate to Severe Atopic Dermatitis
Public ClinicalTrials.gov record NCT06461897. 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.
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 3, Open-label, Efficacy-Assessor-Blinded Study, Comparing the Safety and Efficacy of Upadacitinib to Dupilumab in Children From 2 to Less Than 12 Years of Age With Moderate to Severe Atopic Dermatitis
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. Topical therapies applied over the skin may not be enough to control the AD in trial participants who require systemic anti-inflammatory treatment. This study compares upadacitinib to dupilumab in pediatric participants with moderate to severe AD who are candidates for systemic therapy. Adverse events and change in the disease activity will be assessed. Upadacitinib is an approved drug for treating AD patients aged 12 or older. Participants will receive upadacitinib (given as daily dose) or dupilumab (given at label indicated dose every 2 or 4 weeks). Participants will be stratified depending on disease severity, age and response to previous treatment. There is 1 in 5 chance for participants to receive dupilumab during the randomized cohort. Approximately 675 participants aged 2 to less than 12 years of age will be enrolled in this study at approximately 150 sites worldwide. The study population (As defined by participants age or prior treatment) to be enrolled in the study is dependent on local regulatory requirement and/or agreement. Participants will receive upadacitinib oral tablets once daily (or oral solution twice a day) for 160 weeks, or dupilumab as per its label for 52 weeks, and followed for 30 days after the last dose of upadacitinib and at least 12 weeks after the last dose of dupilumab. 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 clinical assessments, blood tests, checking for side effects and completing questionnaires.
Study identification
- NCT ID
- NCT06461897
- Recruitment status
- Recruiting
- Study type
- Interventional
- Phase
- Phase 3
- Enrollment
- 675 participants
Conditions and interventions
Conditions
Eligibility (public fields only)
- Age range
- 2 Years to 11 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
- Aug 18, 2024
- Primary completion
- Jun 30, 2030
- Completion
- Jun 30, 2030
- Last update posted
- Aug 5, 2026
2024 – 2030
United States locations
- U.S. sites
- 31
- U.S. states
- 19
- U.S. cities
- 30
| Facility | City | State | ZIP | Site status |
|---|---|---|---|---|
| Applied Research Center and Wellness Clinic /ID# 268547 | Little Rock | Arkansas | 72205 | Recruiting |
| Stanford University School of Medicine /ID# 269622 | Palo Alto | California | 94304 | Recruiting |
| Integrative Skin Science and Research /ID# 265108 | Sacramento | California | 95815 | Recruiting |
| Clearlyderm Dermatology - West Boca /ID# 266323 | Boca Raton | Florida | 33428 | Completed |
| Pediatric Skin Research - Coral Gables /ID# 266308 | Coral Gables | Florida | 33146 | Recruiting |
| Neoclinical Research - Hialeah /ID# 269694 | Hialeah | Florida | 33016 | Completed |
| Emory University School Of Medicine - Atlanta /ID# 268832 | Atlanta | Georgia | 30322 | Recruiting |
| Cleaver Medical Group Dermatology /ID# 265099 | Dawsonville | Georgia | 30534 | Completed |
| Aeroallergy Research Laboratory /ID# 267247 | Savannah | Georgia | 31406 | Recruiting |
| Treasure Valley Medical Research /ID# 266838 | Boise | Idaho | 83706 | Recruiting |
| Northwestern University Feinberg School of Medicine /ID# 265117 | Chicago | Illinois | 60611-2927 | Recruiting |
| Sneeze Wheeze & Itch Associates /ID# 267238 | Normal | Illinois | 61761 | Recruiting |
| Dawes Fretzin /ID# 265097 | Indianapolis | Indiana | 46256 | Recruiting |
| Equity Medical, LLC /ID# 268270 | Bowling Green | Kentucky | 42104 | Recruiting |
| Maryland Allergy & Asthma Center /ID# 268032 | Lanham | Maryland | 20706 | Recruiting |
| DermAssociates - Rockville /ID# 266457 | Rockville | Maryland | 20850 | Completed |
| Washington University School of Medicine - St. Louis /ID# 268545 | St Louis | Missouri | 63130 | Recruiting |
| Skin Specialists /ID# 266331 | Omaha | Nebraska | 68144 | Recruiting |
| DOCS Clinical Research - Canal Winchester /ID# 268271 | Canal Winchester | Ohio | 43110-2069 | Recruiting |
| Wright State Physicians Health Center /ID# 268841 | Fairborn | Ohio | 45324 | Recruiting |
| Oregon Health and Science University /ID# 266483 | Portland | Oregon | 97239 | Recruiting |
| Medical University of South Carolina /ID# 265113 | Charleston | South Carolina | 29425 | Recruiting |
| International Clinical Research - Tennessee /ID# 268548 | Murfreesboro | Tennessee | 37130 | Completed |
| Arlington Research Center, Inc /ID# 266330 | Arlington | Texas | 76011 | Recruiting |
| 3A Research - East location /ID# 267622 | El Paso | Texas | 79925 | Recruiting |
| Prime Clinical Research - Mansfield - East Broad Street /ID# 268042 | Mansfield | Texas | 76063 | Recruiting |
| Texas Dermatology and Laser Specialists /ID# 267249 | San Antonio | Texas | 78218 | Recruiting |
| Progressive Clinical Research - San Antonio /ID# 267262 | San Antonio | Texas | 78229 | Recruiting |
| Jordan Valley Dermatology & Research Center /ID# 267092 | South Jordan | Utah | 84095 | Recruiting |
| West Virginia University Hospitals /ID# 265114 | Morgantown | West Virginia | 26506 | Recruiting |
| Medical College Of Wisconsin - Milwaukee Campus /ID# 267236 | Milwaukee | Wisconsin | 53226 | Recruiting |
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 119 non-U.S. sites.
About this trial record page
- What this page shows
- Public field values for ClinicalTrials.gov record NCT06461897, 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 Aug 5, 2026 · Synced Sep 11, 2026
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Open the official record
The complete protocol, eligibility criteria, and contact information for NCT06461897 live on ClinicalTrials.gov.