The objective of this study is to assess the safety of upadacitinib combined with topical corticosteroids (TCS) in adolescent and adult participants in Japan with moderate to severe atopic dermatitis (AD) who are candidates for systemic therapy.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Enrollment
272
Upadacitinib is administered orally.
Placebo is administered orally.
It is administered concomitantly with upadacitinib or placebo.
Number of participants experiencing adverse events
Adverse events are defined as those that began or worsened in severity after the first dose of study drug but within 30 days after the last dose of study drug.
Time frame: Up to 141 Weeks
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Ichinomiya Municipal Hospital /ID# 205942
Ichinomiya-shi, Aichi-ken, Japan
Central Clinic /ID# 206558
Nagoya, Aichi-ken, Japan
Nagoya City University Hospital /ID# 207566
Nagoya, Aichi-ken, Japan
Yasumoto Dermatology Clinic /ID# 206480
Chikushino-shi, Fukuoka, Japan
Kiryu Dermatology Clinic /ID# 206044
Fukuoka, Fukuoka, Japan
Medical Corporation Matsuo Clinic /ID# 207323
Fukuoka, Fukuoka, Japan
Matsuda Tomoko Dermatological Clinic /ID# 206288
Fukuoka, Fukuoka, Japan
Higuchi Dermatology Urology Clinic /ID# 206287
Kasuga-shi, Fukuoka, Japan
Central Japan International Medical Center /ID# 205684
Minokamo-shi, Gifu, Japan
Kiryu Kosei General Hospital /ID# 206155
Kiryu-shi, Gunma, Japan
...and 33 more locations