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Comparison · NCT03170271-84c9d05b

Benralizumab vs Placebo: Time to First Asthma Exacerbation (up to 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: Time to First Asthma Exacerbation (up to Week 24). Trial comparisons, record NCT03170271-84c9d05b. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT03170271-84c9d05b

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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 10.2880.2470.333wilson
Risk in group 20.4670.4040.532wilson
Risk difference, group 1 minus group 2-0.179-0.256-0.102newcombe hybrid score
Risk ratio, group 1 over group 20.6160.5030.756log
Odds ratio, group 1 over group 20.4610.330.644log
Number needed to treat, for one fewer participant with the outcome on Benralizumab than on Placebo5.583.919.85from the risk difference interval

Groups2

Group 2 names the comparator: placebo.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1BenralizumabPatients received benralizumab 30 mg administered sc in an accessorized pre-filled syringe at Week 0 (initial dose), Week 4 (loading dose), Week 8 and Week 16. An EOT visit was performed at Week 24.123427OG000
Group 2Placebo
Patients received matching placebo solution administered sc in an accessorized pre-filled syringe at Week 0 (initial dose), Week 4 (loading dose), Week 8 and Week 16. An EOT visit was performed at Week 24.
107229OG001

Outcome

Type
SECONDARY
Title
Time to First Asthma Exacerbation (up to Week 24)
Description
Time to first asthma exacerbation was derived as follows:~Start date of first asthma exacerbation - Date of randomization + 1. The time to first asthma exacerbation for patients who did not experience an asthma exacerbation during the treatment period was censored at the EOT visit (Week 24) for patients who completed the study. Patients who withdrew from the study or were lost to follow-up before the EOT visit were censored at the last visit date after which an exacerbation could not be assessed. The median time to first asthma exacerbation was not calculated, so the number of patients who experienced an asthma exacerbation is presented for the measured values.
Time frame
Baseline (Week 0) up to Week 24
Population
The FAS included all randomized patients who received at least 1 dose of IP, irrespective of their protocol adherence and continued participation in the study.

Source ClinicalTrials.gov

Trial

Title
A Study of the Safety and Effectiveness of Benralizumab to Treat Patients With Severe Uncontrolled Asthma.
NCT number
NCT03170271
Phases
PHASE3
Conditions
Asthma
Interventions
Benralizumab (Medi-563), Placebo
Lead sponsor
AstraZeneca
Results first posted
2020-12-16

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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