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Comparison · NCT02869438-sae

Benra 30 mg 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. Benra 30 mg vs Placebo: serious adverse events. Trial comparisons, record NCT02869438-sae. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT02869438-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 10.008470.00150.0464wilson
Risk in group 20.06090.02980.12wilson
Risk difference, group 1 minus group 2-0.0524-0.112-0.00333newcombe hybrid score
Risk ratio, group 1 over group 20.1390.01741.11log
Odds ratio, group 1 over group 20.1320.0161.09log
Number needed to treat, for one fewer participant with a serious adverse event on Benra 30 mg than on Placebo19.18.91300from the risk difference interval

Groups2

Group 2 names the comparator: placebo.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1Benra 30 mg12-week treatment period and receive Benra 30 mg at Day 0, Day 28 (±3 days), and Day 56 (±3 days).1118EG000
Group 2Placebo12-week treatment period and receive Placebo at Day 0, Day 28 (±3 days), and Day 56 (±3 days).7115EG001

Harm

What it counts
Total, serious adverse events
Time frame
From informed consent form was signed to end of study (ie, Day 112 follow-up)

Source ClinicalTrials.gov

Trial

Title
A Study to Evaluate the Onset of Effect and Time Course of Change in Lung Function With Benralizumab in Severe, Uncontrolled Asthma Patients With Eosinophilic Inflammation
NCT number
NCT02869438
Phases
PHASE3
Conditions
Asthma
Interventions
Benralizumab, Placebo
Lead sponsor
AstraZeneca
Results first posted
2019-10-07

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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