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Comparison · NCT02322775-sae

Benralizumab 30 mg Q4W vs Placebo: serious adverse events

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 30 mg Q4W vs Placebo: serious adverse events. Trial comparisons, record NCT02322775-sae. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT02322775-sae

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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 10.01890.005190.0662wilson
Risk in group 20.0190.005240.0668wilson
Risk difference, group 1 minus group 2-0.00018-0.04990.0491newcombe hybrid score
Risk ratio, group 1 over group 20.9910.1426.9log
Odds ratio, group 1 over group 20.990.1377.16log
Number needed to treat, for one fewer participant with a serious adverse event on Benralizumab 30 mg Q4W than on Placebo5,560from the risk difference intervalthe interval includes no difference

Groups2

Group 2 names the comparator: placebo.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1Benralizumab 30 mg Q4WBenralizumab administered subcutaneously every 4 weeks2106EG000
Group 2PlaceboPlacebo administered subcutaneously every 4 weeks2105EG001

Harm

What it counts
Total, serious adverse events
Time frame
AEs, including SAEs, in the on-study period were defined as those with onset between day of the first dose of study treatment and last scheduled follow-up visit, inclusive, up to 20 weeks.

Source ClinicalTrials.gov

Trial

Title
Study to Evaluate the Efficacy and Safety of Benralizumab in Adult Patients With Mild to Moderate Persistent Asthma
NCT number
NCT02322775
Phases
PHASE3
Conditions
Asthma
Interventions
Benralizumab, Placebo
Lead sponsor
AstraZeneca
Results first posted
2017-02-14

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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