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Monoclonal Antibodies
Benralizumab for Eosinophilic Gastrointestinal Diseases (HUDSON GI Trial)
Phase 3
Waitlist Available
Led By Marc E. Rothenberg, MD, PhD
Research Sponsored by AstraZeneca
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Symptoms including at least moderate abdominal pain, nausea, bloating, early satiety, and/or loss of appetite
Baseline Eosinophilic gastritis, with or without duodenitis, or eosinophilic duodenitis alone confirmed by biopsy with specific eosinophil counts
Must not have
Helminth parasitic infection diagnosed within 24 weeks prior to the date informed that has not been treated with or has failed to respond to standard of care therapy
Concomitant use of immunosuppressive medication
Timeline
Screening 3 weeks
Treatment Varies
Follow Up week 52
Awards & highlights
Pivotal Trial
Summary
This trial involves using benralizumab to treat patients with inflammation in their stomach or upper small intestine. The medication works by lowering the number of specific cells that cause this inflammation. Patients who participate can receive this treatment for several months.
Who is the study for?
This trial is for people aged 12 and older with a confirmed diagnosis of eosinophilic gastritis or gastroenteritis. They must have certain levels of eosinophils in their stomach or duodenum, experience symptoms like abdominal pain and nausea, and be on stable medication if any. Women who can have children must use effective birth control.
What is being tested?
The study tests Benralizumab against a placebo in patients with eosinophilic gastritis/gastroenteritis. It's divided into three parts: initial randomization (Part A), optional continuation (Part C), and an additional open-label treatment phase (Part D).
What are the potential side effects?
While not specified here, common side effects of drugs like Benralizumab may include headache, sore throat, fever, fatigue, allergic reactions at the injection site, and possible increased risk of infections.
Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowSelect...
I experience moderate to severe stomach issues, including pain and loss of appetite.
Select...
I have been diagnosed with eosinophilic gastritis or duodenitis through a biopsy.
Exclusion Criteria
You may be eligible for the trial if you check “No” for criteria below:Select...
I was diagnosed with a worm infection in the last 24 weeks and treatment didn’t work or I haven’t been treated.
Select...
I am currently taking medication that suppresses my immune system.
Select...
I have been diagnosed with a rare blood disorder or a specific type of vasculitis.
Select...
I have an ongoing liver condition.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ week 52
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~week 52
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
Absolute change from baseline in SAGED (Symptom Assessment for Gastrointestinal Eosinophilic Diseases) Score (range: 0-50). SAGED score measures gastrointestinal symptoms with higher scores meaning worse outcome
Proportion of patients achieving a histological response in the stomach and/or in the duodenum
Secondary study objectives
Clinically meaningful symptom change. Time to clinically meaningful change in SAGED score (range: 0-50) measures gastrointestinal symptoms with higher scores meaning worse outcome.
Constipation
Diarrhea-free days
+12 moreOther study objectives
Safety and tolerability - Incidence of Treatment-Emerged AEs and SAEs
Side effects data
From 2016 Phase 3 trial • 220 Patients • NCT0207525515%
Nasopharyngitis
8%
Asthma
7%
Sinusitis
7%
Headache
7%
Bronchitis
6%
Upper respiratory tract infection
4%
Influenza
3%
Back pain
3%
Cough
3%
Dyspnoea
3%
Hypertension
3%
Rhinitis
1%
Urosepsis
1%
Nephrolithiasis
1%
Intervertebral disc protrusion
1%
Umbilical hernia
1%
Adverse drug reaction
1%
Hypersensitivity
1%
Vertigo
1%
Nausea
1%
Dermatitis atopic
1%
Urinary tract infection bacterial
100%
80%
60%
40%
20%
0%
Study treatment Arm
Benra 30 mg q.4 Weeks
Benra 30 mg q.8 Weeks
Placebo
Awards & Highlights
Pivotal Trial
The final step before approval, pivotal trials feature drugs that have already shown basic safety & efficacy.
Trial Design
2Treatment groups
Experimental Treatment
Placebo Group
Group I: BenralizumabExperimental Treatment1 Intervention
This arm is a subcutaneous dose of Benralizumab
Group II: PlaceboPlacebo Group1 Intervention
This arm is a subcutaneous dose of Placebo
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Benralizumab
2016
Completed Phase 4
~10320
Research Highlights
Information in this section is not a recommendation. We encourage patients to speak with their healthcare team when evaluating any treatment decision.Mechanism Of Action
Side Effect Profile
Prior Approvals
Other Research
The most common treatments for Eosinophilic Gastritis, such as benralizumab, work by targeting and depleting eosinophils, which are white blood cells involved in inflammatory responses. Benralizumab is an anti-eosinophil monoclonal antibody that binds to the IL-5 receptor on eosinophils, leading to their destruction.
This mechanism is crucial for patients with Eosinophilic Gastritis because eosinophils contribute to the inflammation and tissue damage characteristic of the disease. By reducing eosinophil levels, these treatments can alleviate symptoms and improve the quality of life for patients.
Efficacy and Safety of Anti-Interleukin-5 Therapies in Chronic Rhinosinusitis with Nasal Polyps: A Systematic Review and Meta-Analysis of Randomized Controlled Trials.World Health Organization-defined eosinophilic disorders: 2019 update on diagnosis, risk stratification, and management.
Efficacy and Safety of Anti-Interleukin-5 Therapies in Chronic Rhinosinusitis with Nasal Polyps: A Systematic Review and Meta-Analysis of Randomized Controlled Trials.World Health Organization-defined eosinophilic disorders: 2019 update on diagnosis, risk stratification, and management.
Find a Location
Who is running the clinical trial?
AstraZenecaLead Sponsor
4,388 Previous Clinical Trials
289,109,761 Total Patients Enrolled
Marc E. Rothenberg, MD, PhDPrincipal InvestigatorCincinnati Children's Hospital Medical Center 3333 Burnet Ave, Cincinnati Ohio 45229, United States
2 Previous Clinical Trials
245 Total Patients Enrolled
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:- I was diagnosed with a worm infection in the last 24 weeks and treatment didn’t work or I haven’t been treated.I have a current cancer or a history of cancer, with some exceptions.I have been diagnosed with EG/EGE for at least 3 months.I experience moderate to severe stomach issues, including pain and loss of appetite.My medication for EG/EGE has been the same for the last 4 weeks.I am currently taking medication that suppresses my immune system.I have been diagnosed with a rare blood disorder or a specific type of vasculitis.I am 12 years old or older.I have an ongoing liver condition.I have been diagnosed with eosinophilic gastritis or duodenitis through a biopsy.I have a history of specific stomach or bowel issues.I have not received any live vaccines in the last 30 days.
Research Study Groups:
This trial has the following groups:- Group 1: Placebo
- Group 2: Benralizumab
Awards:
This trial has 1 awards, including:- Pivotal Trial - The final step before approval, pivotal trials feature drugs that have already shown basic safety & efficacy.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
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