Comparison · NCT04157335-739b6287
Double Blind Benralizumab vs Double Blind Placebo: Percentage of Participants With SCS Use for CRSwNP
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. Double Blind Benralizumab vs Double Blind Placebo: Percentage of Participants With SCS Use for CRSwNP. Trial comparisons, record NCT04157335-739b6287. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT04157335-739b6287
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Measures6
Calculated by ConductScience from the counts the trial posted to ClinicalTrials.gov.
| Measure | Value | 95% interval, lower | 95% interval, upper | Method | Note |
|---|---|---|---|---|---|
| Risk in group 1 | 0.151 | 0.101 | 0.22 | wilson | |
| Risk in group 2 | 0.163 | 0.11 | 0.234 | wilson | |
| Risk difference, group 1 minus group 2 | -0.0119 | -0.0992 | 0.0749 | newcombe hybrid score | |
| Risk ratio, group 1 over group 2 | 0.927 | 0.535 | 1.61 | log | |
| Odds ratio, group 1 over group 2 | 0.914 | 0.477 | 1.75 | log | |
| Number needed to treat, for one fewer participant with the outcome on Double Blind Benralizumab than on Double Blind Placebo | 84.1 | from the risk difference interval | the interval includes no difference |
Source ClinicalTrials.gov
Groups2
Group 2 names the comparator: placebo.
| Group | Title | Description | With the outcome | Analysed | ClinicalTrials.gov code |
|---|---|---|---|---|---|
| Group 1 | Double Blind Benralizumab | 30 mg Benralizumab administered every 4 weeks subcutaneously for the first 3 doses (Weeks 0, 4 and 8) and every 8 weeks (Q8W) thereafter. | 21 | 139 | OG000 |
| Group 2 | Double Blind Placebo | 30 mg Placebo administered every 4 weeks subcutaneously for the first 3 doses (Weeks 0, 4 and 8) and every 8 weeks (Q8W) thereafter. | 22 | 135 | OG001 |
Source ClinicalTrials.gov
Outcome
- Type
- SECONDARY
- Title
- Percentage of Participants With SCS Use for CRSwNP
- Description
An SCS course can be considered as a new course if the start date is preceded by at least 7 days after the end date of the last SCS course for CRSwNP (i.e. start date of the new course - end date of the last course \> 7)
- Time frame
- Baseline to Week 56
- Population
- Primary full analysis set (All CRSwNP participants with asthma who were randomized and received any IP. N=139 in treatment group and N=135 in placebo).
Source ClinicalTrials.gov
Trial
- Title
- Efficacy and Safety Study of Benralizumab in Patient With Eosinophilic Chronic Rhinosinusitis With Nasal Polyps (ORCHID)
- NCT number
- NCT04157335
- Phases
- PHASE3
- Conditions
- Nasal Polyposis, Eosinophilic Chronic Rhinosinusitis
- Interventions
- Benralizumab 30 mg, Matched placebo
- Lead sponsor
- AstraZeneca
- Results first posted
- 2026-02-19
- Results on ClinicalTrials.gov
- https://clinicaltrials.gov/study/NCT04157335?tab=results
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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