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Comparison · NCT04333732-6af0815e

M-M-R II ® vs Placebo: Risk of SARS-CoV-2 Infection up to 150 Days After Trial Intervention

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. M-M-R II ® vs Placebo: Risk of SARS-CoV-2 Infection up to 150 Days After Trial Intervention. Trial comparisons, record NCT04333732-6af0815e. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT04333732-6af0815e

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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 10.1060.08780.127wilson
Risk in group 20.1030.08530.124wilson
Risk difference, group 1 minus group 20.00277-0.02490.0304newcombe hybrid score
Risk ratio, group 1 over group 21.030.7891.34log
Odds ratio, group 1 over group 21.030.7671.38log
Number needed to treat, for one more participant with the outcome on M-M-R II ® than on Placebo361from the risk difference intervalthe interval includes no difference

Groups2

Group 2 names the comparator: placebo.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1M-M-R II ®Education and surveillance plus M-M-R II ® Single dose, 0.5 mL subcutaneous injection of M-M-R II ®~MR or M-M-R II ® vaccine: Education and surveillance plus MR or M-M-R II ® vaccine100945OG000
Group 2PlaceboEducation and surveillance plus placebo Single dose, 0.5 mL subcutaneous injection of 0.9% saline~Placebo: Placebo injection98951OG001

Outcome

Type
SECONDARY
Title
Risk of SARS-CoV-2 Infection up to 150 Days After Trial Intervention
Description
Risk of SARS-CoV-2 infection by serology (anti-nucleocapsid antibody) in the intervention and control groups in adults with repeated exposures to SARS-CoV-2 by day 150 after receiving trial intervention. Infection with SARS CoV-2 during the course of the trial was diagnosed when IgG antibodies to the viral nucleocapsid protein were present from the 150 day specimen, but not the baseline specimen.
Time frame
150 days
Population

Source ClinicalTrials.gov

Trial

Title
CROWN CORONATION: COVID-19 Research Outcomes Worldwide Network for CORONAvirus prevenTION
NCT number
NCT04333732
Phases
PHASE3
Conditions
COVID 19
Interventions
MR or M-M-R II ® vaccine, Placebo
Lead sponsor
Washington University School of Medicine
Results first posted
2024-03-26

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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