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A Study to Evaluate Safety of Upadacitinib in Combination With Topical Corticosteroids in Adolescent and Adult Participants With Moderate to Severe Atopic Dermatitis

Phase 3
Completed
Conditions
Atopic Dermatitis
Interventions
Drug: Topical Corticosteroids (TCS)
Registration Number
NCT03661138
Lead Sponsor
AbbVie
Brief Summary

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.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
272
Inclusion Criteria
  • Active moderate to severe atopic dermatitis defined by Eczema Area and Severity Index (EASI), Investigator's Global Assessment (IGA), Body surface area (BSA), and pruritus.
  • Candidate for systemic therapy or have recently required systemic therapy for atopic dermatitis.
  • Able to tolerate topical corticosteroids for atopic dermatitis lesions.
Exclusion Criteria
  • Prior exposure to any Janus kinase (JAK) inhibitor.
  • Unable or unwilling to discontinue current atopic dermatitis (AD) treatments prior to the study.
  • Requirement of prohibited medications during the study.
  • Female participant who is pregnant, breastfeeding, or considering pregnancy during the study.

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Arm BTopical Corticosteroids (TCS)Upadacitinib Dose B is administered once daily along with Topical Corticosteroids (TCS).
Arm CPlacebo for upadacitinibPlacebo administered once daily and TCS followed by Upadacitinib Dose A once daily along with TCS.
Arm ATopical Corticosteroids (TCS)Upadacitinib Dose A is administered once daily along with Topical Corticosteroids (TCS).
Arm DPlacebo for upadacitinibPlacebo administered once daily and TCS followed by Upadacitinib Dose B once daily along with TCS.
Arm DTopical Corticosteroids (TCS)Placebo administered once daily and TCS followed by Upadacitinib Dose B once daily along with TCS.
Arm CTopical Corticosteroids (TCS)Placebo administered once daily and TCS followed by Upadacitinib Dose A once daily along with TCS.
Arm AUpadacitinibUpadacitinib Dose A is administered once daily along with Topical Corticosteroids (TCS).
Arm BUpadacitinibUpadacitinib Dose B is administered once daily along with Topical Corticosteroids (TCS).
Arm CUpadacitinibPlacebo administered once daily and TCS followed by Upadacitinib Dose A once daily along with TCS.
Arm DUpadacitinibPlacebo administered once daily and TCS followed by Upadacitinib Dose B once daily along with TCS.
Primary Outcome Measures
NameTimeMethod
Number of participants experiencing adverse eventsUp to 141 Weeks

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.

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (43)

Fukuyama City Hospital /ID# 206761

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Fukuyama-shi, Hiroshima, Japan

Nagoya City University Hospital /ID# 207566

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Nagoya shi, Aichi, Japan

Central Clinic /ID# 206558

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Nagoya-shi, Aichi, Japan

Kiryu Dermatology Clinic /ID# 206044

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Fukuoka-shi, Fukuoka, Japan

Ichinomiya Municipal Hospital /ID# 205942

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Ichinomiya-shi, Aichi, Japan

Yasumoto Dermatology Clinic /ID# 206480

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Chikushino-shi, Fukuoka, Japan

Matsuda Tomoko Dermatological Clinic /ID# 206288

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Fukuoka-shi, Fukuoka, Japan

Nagasaki University Hospital /ID# 206118

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Nagasaki-shi, Nagasaki, Japan

Medical Corporation Matsuo Clinic /ID# 207323

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Fukuoka-shi, Fukuoka, Japan

Gunma University Hospital /ID# 207016

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Maebashi-shi, Gunma, Japan

Asahikawa Medical University Hospital /ID# 206521

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Asahikawa-shi, Hokkaido, Japan

Kitago Dermatology Clinic /ID# 207025

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Sapporo-shi, Hokkaido, Japan

Hokkaido P.W.F.A.C. Sapporo-Kosei General Hospital /ID# 206519

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Sapporo-shi, Hokkaido, Japan

Mita Dermatology /ID# 206694

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Minato-ku, Tokyo, Japan

Medical Corporation Jitai-kai Nakano Dermatology Clinic /ID# 206882

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Nakano-ku, Tokyo, Japan

Tampopo Dermatology Clinic /ID# 207013

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Ota-ku, Tokyo, Japan

Toyama Prefectural Central Hospital /ID# 206286

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Toyama-shi, Toyama, Japan

Naoko Dermatology Clinic /ID# 205334

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Setagaya-ku, Tokyo, Japan

Tachikawa Dermatology Clinic /ID# 206996

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Tachikawa-shi, Tokyo, Japan

Kobe University Hospital /ID# 206200

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Kobe-shi, Hyogo, Japan

Central Japan International Medical Center /ID# 205684

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Minokamo-shi, Gifu, Japan

Kiryu Kosei General Hospital /ID# 206155

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Kiryu-shi, Gunma, Japan

Higuchi Dermatology Urology Clinic /ID# 206287

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Kasuga-shi, Fukuoka, Japan

Medical Corporation Kato Dermatology Clinic /ID# 206561

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Sapporo-shi, Hokkaido, Japan

Kansai Rosai Hospital /ID# 205918

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Amagasaki-shi, Hyogo, Japan

Hyogo Prefectural Amagasaki General Medical Center /ID# 206974

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Amagasaki-shi, Hyogo, Japan

Nippon Medical School Musashi Kosugi Hospital /ID# 206656

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Kawasaki-shi, Kanagawa, Japan

Tokai University Hospital /ID# 206657

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Isehara-shi, Kanagawa, Japan

Medical corporation Kojunkai Kosugi Dermatology Clinic /ID# 206766

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Kawasaki-shi, Kanagawa, Japan

Yokohama Rosai Hospital /ID# 206648

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Yokohama-shi, Kanagawa, Japan

Suizenji Dermatology Clinic /ID# 205871

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Kumamoto-shi, Kumamoto, Japan

Nagaoka Red Cross Hospital /ID# 209817

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Nagaoka-shi, Niigata, Japan

Isonokami dermatological clinic /ID# 206923

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Daito-shi, Osaka, Japan

Shizuoka General Hospital /ID# 207122

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Shizuoka-shi, Shizuoka, Japan

Medical corporation Kojinkai Yoshioka Dermatology Clinic /ID# 209704

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Neyagawa-shi, Osaka, Japan

Mildix Skin Clinic /ID# 206829

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Adachi-ku, Tokyo, Japan

Hosono Clinic /ID# 205953

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Chuo-ku, Tokyo, Japan

Yaesu Nihonbashi Skin Clinic /ID# 207125

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Chuo-ku, Tokyo, Japan

Fukuwa clinic /ID# 206760

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Chuo-ku, Tokyo, Japan

Nihon University Itabashi Hospital /ID# 206186

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Itabashi-ku, Tokyo, Japan

Matsuyama Dermatology /ID# 205998

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Nakano-ku, Tokyo, Japan

Miu Skin Clinic /ID# 206911

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Ota-ku, Tokyo, Japan

Tokyo Rosai Hospital /ID# 205809

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Ota-ku, Tokyo, Japan

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