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RECRUITING
NCT07023302
PHASE3

A Study to Evaluate the Safety and Effectiveness of Upadacitinib Tablets in Adult and Adolescent Participants in Japan With Alopecia Areata

Sponsor: AbbVie

View on ClinicalTrials.gov

Summary

Alopecia areata (AA) is a disease that happens when the immune system attacks hair follicles and causes hair loss. AA usually affects the head and face, but hair loss can happen on any part of the body. The purpose of this study is to assess how safe, effective, and tolerable upadacitinib is in adolescent and adult participants in Japan with severe AA. Upadacitinib is an approved drug being investigated for the treatment of AA. In Period A, participants are placed in 1 of 3 groups, called treatment arms. Each group receives a different treatment. There is a 1 in 3 chance that participants will be assigned to placebo. In Period B, participants originally randomized to a upadacitinib dose group in Period A will continue their same treatment in Period B. Participants originally randomized to Placebo in Period A will be re-randomized in 1 of 2 groups receiving upadacitinib. Participants who complete Period B can join Period C and will receive 1 of 2 doses of upadacitinib for up to 52 weeks based on their SALT score. Around 123 adolescent and adult participants with severe AA will be enrolled in the study at approximately 20 sites in Japan. Participants will receive oral tablets of either upadacitinib or placebo once daily for up to 104 weeks with the potential of being re-randomized into a different treatment group at Weeks 24 and 52. Participants will be followed up for up to 30 days after their last study drug dose. 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.

Official title: A Phase 3 Randomized, Placebo-Controlled, Double-Blind Study to Evaluate Efficacy and Safety of Upadacitinib in Adult and Adolescent Subjects With Alopecia Areata and at Least 25% Scalp Hair Loss

Key Details

Gender

All

Age Range

12 Years - 63 Years

Study Type

INTERVENTIONAL

Enrollment

123

Start Date

2025-06-19

Completion Date

2029-02

Last Updated

2025-12-24

Healthy Volunteers

No

Conditions

Interventions

DRUG

Upadacitinib

Oral Tablets

DRUG

Upadacitinib Placebo

Oral Tablets

Locations (15)

Nagoya City University Hospital /ID# 275409

Nagoya, Aichi-ken, Japan

Kurume University Hospital /ID# 275519

Kurume-shi, Fukuoka, Japan

Kanazawa Medical University Hospital /ID# 275521

Kahoku-gun, Ishikawa-ken, Japan

Nagomi Dermatology Clinic /ID# 275418

Ebina-shi, Kanagawa, Japan

Rifu Dermatology Allergy Clinic /ID# 274875

Miyagi-gun, Miyagi, Japan

Tohoku University Hospital /ID# 274931

Sendai, Miyagi, Japan

Niigata University Medical & Dental Hospital /ID# 274775

Niigata, Niigata, Japan

Shinsaibashi Inui Dermatology Clinic /ID# 274851

Osaka, Osaka, Japan

Osaka Metropolitan University Hospital /ID# 274956

Osaka, Osaka, Japan

Hamamatsu University Hospital /ID# 274639

Hamamatsu, Shizuoka, Japan

Kyorin University Hospital /ID# 274882

Mitaka-shi, Tokyo, Japan

Tokyo Medical University Hospital /ID# 274844

Shinjuku-ku, Tokyo, Japan

Keio University Hospital /ID# 275640

Shinjuku-ku, Tokyo, Japan

Yamaguchi University Hospital /ID# 274638

Ube, Yamaguchi, Japan

Juntendo Tokyo Koto Geriatric Medical Center /ID# 275424

Tokyo, Japan