CI

At a glance

ClinicalIndex Comparison Record
Phase 3Active· 1,533 enrolled
Drug / intervention
Placebo +2 moredrug
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT03568318
NCT03568318Phase 3Active

A Phase 3 Randomized, Placebo-Controlled, Double-Blind Study to Evaluate Upadacitinib in Combination With Topical Corticosteroids in Adolescent and Adult Subjects With Moderate to Severe Atopic Dermatitis

AbbVie·interventional·Posted Jun 26, 2018·Updated Dec 23, 2025

In Brief

A Phase 3 clinical trial evaluating Placebo, Upadacitinib, and 1 other intervention for Atopic Dermatitis. Active but no longer recruiting, targeting 1,533 participants across 193 sites in 24 countries.

Detailed Summary

The objective of this study is to assess the efficacy and safety of upadacitinib combined with topical corticosteroids (TCS) for the treatment of adolescent and adult participants with moderate to severe atopic dermatitis (AD) who are candidates for systemic therapy.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesAustralia, Austria, Belgium, Canada, China, Czechia, France, Germany, Greece, Hong Kong, Hungary, Ireland, Israel, Italy, Japan, Netherlands, New Zealand, Norway, Puerto Rico, Slovakia, Spain, Sweden, United Kingdom, United States
Collaborators--

Timeline

Phase 3Active
2019202020212022202320242025202620272028202920302031
First PostedJun 26, 2018
Enrollment StartAug 9, 2018
Primary CompletionFeb 16, 2021
Study CompletionOct 23, 2030
TodayJul 2, 2026
Enrollment to primary: 2.5 yearsPosted 8.0 years ago

Interventions

Placebodrug

Tablets taken orally once a day

Upadacitinibdrug

Tablets taken orally once a day

Topical corticosteroids (TCS)drug

Topical corticosteroids will be applied in a stepdown regimen, starting with medium potency once daily to areas with active lesions until lesions are clear or almost clear, or for 3 consecutive weeks, whichever is shorter; then low potency topical corticosteroids once daily. If lesions return or persist, this step-down approach will be repeated until lesion resolution or evidence of local or systemic topical corticosteroids toxicity. Recommended TCS include triamcinolone acetonide 0.1% cream or fluocinolone acetonide 0.025% ointment as medium potency topical corticosteroids and hydrocortisone 1% cream as low potency topical corticosteroid.