ConductScience.org, home

Comparison · NCT04399980-7943564c

Intervention vs Control: Mortality at Day 28

Calculated by ConductScience from the counts the trial posted to ClinicalTrials.gov.

2 sourcestrial-comparisons-2026-03-23-0.1.0

Download JSON
Cite this record

ConductScience Library. Intervention vs Control: Mortality at Day 28. Trial comparisons, record NCT04399980-7943564c. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT04399980-7943564c

On this page

Measures6

Calculated by ConductScience from the counts the trial posted to ClinicalTrials.gov.

MeasureValue95% interval, lower95% interval, upperMethodNote
Risk in group 10.04760.008460.227wilson
Risk in group 20.1580.05520.376wilson
Risk difference, group 1 minus group 2-0.11-0.3320.0962newcombe hybrid score
Risk ratio, group 1 over group 20.3020.03422.66log
Odds ratio, group 1 over group 20.2670.02532.81log
Number needed to treat, for one fewer participant with the outcome on Intervention than on Control9.07from 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 IV121OG000
Group 2ControlOne-time placebo infusion via IV319OG001

Outcome

Type
SECONDARY
Title
Mortality at Day 28
Description
Number and percentage of patients that expired by 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.

For software

Read this comparison from software.

The record is JSON. No key.

GET https://conductscience.org/api/comparisons/v1/NCT04399980-7943564c