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Part A (Blinded): mRNA-1273 vs Part A (Blinded): Placebo: Part A: Number of Participants With a First Occurrence of COVID-19 Starting 14 Days After First Dose

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

Measures 6

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

MeasureValue95% interval, lower95% interval, upperMethodNoteSource
Risk in group 10.003920.003020.00509wilsonClinicalTrials.gov
Risk in group 20.05430.05070.0581wilsonClinicalTrials.gov
Risk difference, group 1 minus group 2-0.0504-0.0543-0.0466newcombe hybrid scoreClinicalTrials.gov
Risk ratio, group 1 over group 20.07220.05510.0946logClinicalTrials.gov
Odds ratio, group 1 over group 20.06850.05220.09logClinicalTrials.gov
Number needed to treat, for one fewer participant with the outcome on Part A (Blinded): mRNA-1273 than on Part A (Blinded): Placebo19.918.421.5from the risk difference intervalClinicalTrials.gov

Groups 2

Group 2 names the comparator: placebo.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov codeSource
Group 1Part A (Blinded): mRNA-1273Participants received 100 μg mRNA-1273 on a 2-dose injection schedule (Day 1 and Day 29).5614,287OG001ClinicalTrials.gov
Group 2Part A (Blinded): PlaceboParticipants received mRNA-1273-matching placebo on a 2-dose injection schedule (Day 1 and Day 29).76914,164OG000ClinicalTrials.gov

Outcome 5

FieldValueSource
TypeSECONDARYClinicalTrials.gov
TitlePart A: Number of Participants With a First Occurrence of COVID-19 Starting 14 Days After First DoseClinicalTrials.gov
Description
COVID-19 cases were defined as participants meeting clinical criteria based both on symptoms for COVID-19 and on RT-PCR detection of SARS-CoV-2 from samples collected within 72 hours of the study participant reporting symptoms that met the definition of COVID-19.~An adjudication committee was assembled for the purpose of reviewing potential cases to determine if the criteria for COVID-19 were met.
ClinicalTrials.gov
Time frameFrom 14 days after first dose up to approximately 8 monthsClinicalTrials.gov
PopulationPart A PP Set. Number analyzed=participants evaluable at specified timepoint.ClinicalTrials.gov

Trial 8

FieldValueSource
TitleA Study to Evaluate Efficacy, Safety, and Immunogenicity of mRNA-1273 Vaccine in Adults Aged 18 Years and Older to Prevent COVID-19ClinicalTrials.gov
NCT numberNCT04470427ClinicalTrials.gov
PhasesPHASE3ClinicalTrials.gov
ConditionsSARS-CoV-2ClinicalTrials.gov
InterventionsmRNA-1273, PlaceboClinicalTrials.gov
Lead sponsorModernaTX, Inc.ClinicalTrials.gov
Results first posted2024-03-21ClinicalTrials.gov
Results on ClinicalTrials.govhttps://clinicaltrials.gov/study/NCT04470427?tab=resultsClinicalTrials.gov

Source 4

FieldValueSource
Releasetrial-comparisons-2026-03-23-0.1.0ClinicalTrials.gov
Release manifest SHA-256f66225897fbf258b57ea10bdacfd0347d3cdfda93f7f5685234b7e06ea36fa57ClinicalTrials.gov
AACT copy2026-03-23ClinicalTrials.gov
Tables readoutcome_counts.parquet, outcome_measurements.parquet, outcomes.parquet, reported_event_totals.parquet, reported_events.parquet, result_groups.parquet, studies.parquet, ctgov_trial.parquetClinicalTrials.gov

The same record as JSON

Release trial-comparisons-2026-03-23-0.1.0

ClinicalTrials.gov's posted results, through CTTI's AACT: ClinicalTrials.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.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.

ClinicalTrials.gov: none 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.