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Comparison · NCT04399980-a5cb368a

Intervention vs Control: Number of Subjects Alive and Without Respiratory Failure at Day 28

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. Intervention vs Control: Number of Subjects Alive and Without Respiratory Failure at Day 28. Trial comparisons, record NCT04399980-a5cb368a. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT04399980-a5cb368a

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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 10.9520.7730.992wilson
Risk in group 20.7890.5670.915wilson
Risk difference, group 1 minus group 20.163-0.05570.389newcombe hybrid score
Risk ratio, group 1 over group 21.210.9381.55log
Odds ratio, group 1 over group 25.330.53952.7log
Number needed to treat, for one more participant with the outcome on Intervention than on Control6.14from the risk difference intervalthe interval includes no difference

Groups2

Group 2 names the comparator: control.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1InterventionOne-time Mavrilimumab infusion at 6mg/kg via IV2021OG000
Group 2ControlOne-time placebo infusion via IV1519OG001

Outcome

Type
SECONDARY
Title
Number of Subjects Alive and Without Respiratory Failure at Day 28
Description
Number and percentage of subjects that are alive and without respiratory failure at Day 28
Time frame
Day 28
Population

Source ClinicalTrials.gov

Trial

Title
Mavrilimumab to Reduce Progression of Acute Respiratory Failure in COVID-19 Pneumonia and Systemic Hyper-inflammation
NCT number
NCT04399980
Phases
PHASE2
Conditions
COVID 19, SARS-CoV 2, Pneumonia
Interventions
Mavrilimumab, Placebos
Lead sponsor
The Cleveland Clinic
Results first posted
2021-05-13

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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