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Comparison · NCT04382586-sae

Zanubrutinib + Supportive Care vs Placebo + Supportive Care: 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. Zanubrutinib + Supportive Care vs Placebo + Supportive Care: serious adverse events. Trial comparisons, record NCT04382586-sae. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT04382586-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 10.1330.05310.297wilson
Risk in group 20.2410.1220.421wilson
Risk difference, group 1 minus group 2-0.108-0.3050.0943newcombe hybrid score
Risk ratio, group 1 over group 20.5520.1811.69log
Odds ratio, group 1 over group 20.4840.1251.87log
Number needed to treat, for one fewer participant with a serious adverse event on Zanubrutinib + Supportive Care than on Placebo + Supportive Care9.26from the risk difference intervalthe interval includes no difference

Groups2

Neither group, or both, names a comparator, so the groups keep ClinicalTrials.gov's order.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1Zanubrutinib + Supportive CareZanubrutinib 320 mg orally once daily for 28 days. Supportive care treatment selected and administered as deemed appropriate by the study investigator.430EG000
Group 2Placebo + Supportive CarePlacebo orally once daily for 28 days. Supportive care treatment selected and administered as deemed appropriate by the study investigator.729EG001

Harm

What it counts
Total, serious adverse events
Time frame
Up to 7 months

Source ClinicalTrials.gov

Trial

Title
Covid-19 Infection and Pulmonary Distress Treatment With Zanubrutinib in Hospitalized Participants
NCT number
NCT04382586
Phases
PHASE2
Conditions
COVID-19 Pulmonary Complications, COVID-19
Interventions
Zanubrutinib, Supportive Care, Placebo
Lead sponsor
BeiGene
Results first posted
2022-03-02

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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