Study identifier:D3258C00001
ClinicalTrials.gov identifier:NCT05251909
EudraCT identifier:2021-000085-14
CTIS identifier:N/A
A Multi-center, Randomized, Double-blind, Parallel-group, Placebo-controlled 3-Part Phase 3 Study to Demonstrate the Efficacy and Safety of Benralizumab in Patients with Eosinophilic Gastritis and/or Gastroenteritis (The HUDSON GI Study)
Eosinophilic gastritis
Phase 3
No
-
All
12
Interventional
12 Years - 130 Years
Allocation: Randomized
Endpoint Classification: -
Intervention Model: Parallel Assignment
Masking: -
Primary Purpose: Treatment
Verified 01 Feb 2024 by AstraZeneca
AstraZeneca
-
No locations available
Arms | Assigned Interventions |
---|---|
Experimental: Benralizumab This arm is a subcutaneous dose of Benralizumab | Biological/Vaccine: Benralizumab Benralizumab is a humanized, afucosylated, monoclonal antibody that binds specifically to the IL-5Rα on the target cell and thus directly depletes eosinophils through antibody-dependent cell-mediated cytotoxicity. Benralizumab has been widely approved for treatment of asthma. Other Name: Fasenra |
Placebo Comparator: Placebo This arm is a subcutaneous dose of Placebo | Biological/Vaccine: Placebo Placebo will be injected as a comparator to injection with Benralizumab to examine effect on both the signs and symptoms of EG/EGE and the underlying eosinophilic inflammation, with dual primary outcome variables |