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好酸球性胃炎および/または胃腸炎患者におけるベンラリズマブの有効性と安全性(HUDSON GI試験)

基本情報

NCT ID
NCT05251909
ステータス
中止
試験のフェーズ
第3相
試験タイプ
介入
目標被験者数
12
治験依頼者名
AstraZeneca

概要

This is a 3-part study. Part A is randomized, double-blinded, placebo-controlled and includes patients with eosinophilic gastritis and/or duodenal-only disease. After completing Part A, participants can continue to Part C - open-label benralizumab treatment period. Following the decision to close enrollment, patients in both Part A and Part C will be given the option to proceed to 6-months of open-label benralizumab treatment in Part D.

対象疾患

Eosinophilic GastritisEosinophilic Gastroenteritis

介入

Benralizumab(BIOLOGICAL)
Placebo(BIOLOGICAL)

依頼者(Sponsor)