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Comparison · NCT04649151-31856bbd

Part 1A: mRNA-1273 100 μg vs Part 1A: Placebo: Part 1A Number of Participants With Asymptomatic SARS-CoV-2 Infection

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. Part 1A: mRNA-1273 100 μg vs Part 1A: Placebo: Part 1A Number of Participants With Asymptomatic SARS-CoV-2 Infection. Trial comparisons, record NCT04649151-31856bbd. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT04649151-31856bbd

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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 10.009340.006050.0144wilson
Risk in group 20.01530.009460.0247wilson
Risk difference, group 1 minus group 2-0.00599-0.0160.00175newcombe hybrid score
Risk ratio, group 1 over group 20.6090.3171.17log
Odds ratio, group 1 over group 20.6060.3121.17log
Number needed to treat, for one fewer participant with the outcome on Part 1A: mRNA-1273 100 μg than on Part 1A: Placebo167from the risk difference intervalthe interval includes no difference

Groups2

Group 2 names the comparator: placebo.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1Part 1A: mRNA-1273 100 μgParticipants received at least 1 of 2 doses of 100 μg mRNA-1273 by IM injection (Day 1 and Day 29).202,142OG000
Group 2Part 1A: PlaceboParticipants received at least 1 of 2 doses of placebo matched to mRNA-1273 100 μg by IM injection (Day 1 and Day 29).161,044OG001

Outcome

Type
SECONDARY
Title
Part 1A Number of Participants With Asymptomatic SARS-CoV-2 Infection
Description
Asymptomatic SARS-CoV-2 infection was defined as absence of symptoms and a positive RT-PCR or serology test (bAb levels against SARS-CoV-2 nucleocapsid protein) post dosing in participants who did not have an infection at baseline or pre-Dose 1.
Time frame
Day 43 (14 days after second injection) up to a median follow up of 2.5 months after second injection
Population
Part 1A PP Set for Efficacy: all randomized participants who received planned doses of study drug, had no immunologic or virologic evidence of prior COVID-19, and had no major protocol deviations that impact key or critical efficacy data.

Source ClinicalTrials.gov

Trial

Title
A Study to Evaluate the Safety, Reactogenicity, and Effectiveness of mRNA-1273 Vaccine in Adolescents 12 to <18 Years Old to Prevent COVID-19
NCT number
NCT04649151
Phases
PHASE2, PHASE3
Conditions
SARS-CoV-2
Interventions
mRNA-1273, Placebo, mRNA-1273.222
Lead sponsor
ModernaTX, Inc.
Results first posted
2025-09-15

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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