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Comparison · NCT05251909-cffe7ca0

Benralizumab vs Placebo: Proportion of Patients With a Histologic Response at Week 24

Calculated by ConductScience from the counts the trial posted to ClinicalTrials.gov.

2 sourcestrial-comparisons-2026-03-23-0.1.0

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ConductScience Library. Benralizumab vs Placebo: Proportion of Patients With a Histologic Response at Week 24. Trial comparisons, record NCT05251909-cffe7ca0. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT05251909-cffe7ca0

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Measures6

Calculated by ConductScience from the counts the trial posted to ClinicalTrials.gov.

MeasureValue95% interval, lower95% interval, upperMethodNote
Risk in group 10.8330.4360.97wilson
Risk in group 200.00000000000000002780.39wilson
Risk difference, group 1 minus group 20.8330.2770.97newcombe hybrid score
Risk ratio, group 1 over group 2loga group has no participants with the outcome
Odds ratio, group 1 over group 2loga cell of the two-by-two table is zero
Number needed to treat, for one more participant with the outcome on Benralizumab than on Placebo1.21.033.61from the risk difference interval

Groups2

Group 2 names the comparator: placebo.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1BenralizumabPatients received benralizumab 30mg every 4 weeks for the 24 weeks treatment period56OG000
Group 2PlaceboPatients received matching Placebo every 4 weeks for the 24 weeks treatment period06OG001

Outcome

Type
PRIMARY
Title
Proportion of Patients With a Histologic Response at Week 24
Description
the proportion of patients achieving a histological response at Week 24, is defined as below:~* 6 eosinophils/hpf in the stomach for the patients with only gastric disease at baseline.~* 6 eosinophils/hpf in the stomach and ≤15 eosinophils/hpf in the duodenum for the patients with gastric + duodenal disease at baseline.~* 15 eosinophils/hpf in the duodenum for the patients with only duodenal disease at baseline.
Time frame
at week 24
Population

Source ClinicalTrials.gov

Trial

Title
Efficacy and Safety of Benralizumab in Patients With Eosinophilic Gastritis and/or Gastroenteritis (The HUDSON GI Study)
NCT number
NCT05251909
Phases
PHASE3
Conditions
Eosinophilic Gastritis, Eosinophilic Gastroenteritis
Interventions
Benralizumab, Placebo
Lead sponsor
AstraZeneca
Results first posted
2025-07-14

Source ClinicalTrials.gov

Source

Release
trial-comparisons-2026-03-23-0.1.0
Release manifest SHA-256
f66225897fbf258b57ea10bdacfd0347d3cdfda93f7f5685234b7e06ea36fa57
AACT copy
2026-03-23
Tables read
outcome_counts.parquet, outcome_measurements.parquet, outcomes.parquet, reported_event_totals.parquet, reported_events.parquet, result_groups.parquet, studies.parquet, ctgov_trial.parquet

Source ClinicalTrials.gov

Sources 2

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNo license stated
Each source's terms
  • ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
  • ClinicalTrials.govnone stated

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions. The measures are ConductScience's calculation from them.

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