🏥 治験ポータル
← 治験一覧に戻る

中等度から重度のアトピー性皮膚炎の成人患者を対象とした、経口ウパダシチニブ錠の目標治療効果と投与量の柔軟性を評価する試験

基本情報

NCT ID
NCT05507580
ステータス
完了
試験のフェーズ
第4相
試験タイプ
介入
目標被験者数
461
治験依頼者名
AbbVie

概要

Atopic dermatitis (AD) is a skin condition that may cause a rash and itching due to inflammation of the skin. Therapies spread over the skin may not be enough to control the AD in trial participants who require systemic anti-inflammatory treatment. This study evaluates the dosing flexibility of upadacitinib in adult participants with moderate to severe AD. Adverse events and change in the disease activity will be assessed. Upadacitinib is an approved drug for the treatment of moderate to severe/active immune-mediated inflammatory diseases such as rheumatoid arthritis, psoriatic arthritis, ankylosing spondylitis, ulcerative colitis (UC), Crohn's Disease (CD), and AD. The study is comprised of a 35-day Screening Period, a 12-week double-blind period and a 12-week single-blind period. During the double-blind period, participants are placed in 1 of 2 groups, called treatment arms and will be randomized in a 1:1 ratio to receive upadacitinib. At 12 weeks during the single blind period, participants will be blinded to the upadacitinib dose based on their EASI response and reassigned to in 1 of 4 arms. After the last study visit, there is a 30-day follow-up visit. Approximately 454 adult participants ages 18 to 64 with moderate to severe AD who are candidates for systemic therapy will be enrolled at up to 160 sites worldwide. The study is comprised of a 12-week double-blind period, followed by a 12-week single-blind period. Participants will receive upadacitinib oral tablets once daily for up to 24 weeks. There may be higher treatment burden for participants in this trial compared to their standard of care (due to study procedures). 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.

対象疾患

Atopic Dermatitis

介入

Upadacitinib(DRUG)

依頼者(Sponsor)

実施施設 (6)

福岡大学病院

Fukuoka, Fukuoka, Japan

東北大学病院

Sendai, Miyagi, Japan

宮田胃腸内科皮膚科クリニック

Matsudo-Shi, Chiba, Japan

たかぎ皮膚科クリニック

Obihiro-shi, Hokkaido, Japan

野村皮フ科

Yokohama, Kanagawa, Japan

まるやま皮膚科クリニック

Koto-ku, Tokyo, Japan