ConductScience.org, home

Comparison · NCT02419937-sae

Tocilizumab vs Placebo: serious adverse events

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. Tocilizumab vs Placebo: serious adverse events. Trial comparisons, record NCT02419937-sae. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT02419937-sae

On this page

Measures6

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

MeasureValue95% interval, lower95% interval, upperMethodNote
Risk in group 10.09090.01620.377wilson
Risk in group 20.1250.0350.36wilson
Risk difference, group 1 minus group 2-0.0341-0.2810.266newcombe hybrid score
Risk ratio, group 1 over group 20.7270.07487.07log
Odds ratio, group 1 over group 20.70.05558.82log
Number needed to treat, for one fewer participant with a serious adverse event on Tocilizumab than on Placebo29.3from the risk difference intervalthe interval includes no difference

Groups2

Group 2 names the comparator: placebo.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1TocilizumabBlinded subjects will be randomized to tocilizumab 162 mg subcutaneously once.~Tocilizumab: 162 mg subcutaneously once (vs. 0.9% normal saline placebo injection once in placebo arm)111EG000
Group 2PlaceboBlinded subjects will be randomized to placebo~Placebo: Saline injection216EG001

Harm

What it counts
Total, serious adverse events
Time frame
Major adverse cardiac event (MACE) rate consisting of several outcomes reported herein were collected 30 days after enrollment

Source ClinicalTrials.gov

Trial

Title
Short-Term Application of Tocilizumab Following Myocardial Infarction
NCT number
NCT02419937
Phases
NA
Conditions
Myocardial Infarction
Interventions
Tocilizumab, Placebo
Lead sponsor
Keesler Air Force Base Medical Center
Results first posted
2017-11-17

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/NCT02419937-sae