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S-268019-b vs Placebo: Number of Participants With First Occurrence of SARS-CoV-2 RT-PCR-Positive Severe COVID-19 in the Initial Vaccination Period

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 1000.000686wilsonClinicalTrials.gov
Risk in group 20.0003570.00006290.00202wilsonClinicalTrials.gov
Risk difference, group 1 minus group 2-0.000357-0.002020.00039newcombe hybrid scoreClinicalTrials.gov
Risk ratio, group 1 over group 2loga group has no participants with the outcomeClinicalTrials.gov
Odds ratio, group 1 over group 2loga cell of the two-by-two table is zeroClinicalTrials.gov
Number needed to treat, for one fewer participant with the outcome on S-268019-b than on Placebo2,805from the risk difference intervalthe interval includes no differenceClinicalTrials.gov

Groups 2

Group 2 names the comparator: placebo.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov codeSource
Group 1S-268019-bParticipants received a dose of S-268019-b via intramuscular injection on Day 1 and Day 29 during the Initial Vaccination Period.05,596OG000ClinicalTrials.gov
Group 2PlaceboParticipants received a dose of placebo via intramuscular injection (matching S-268019-b) on Day 1 and Day 29 during the Initial Vaccination Period.12,805OG001ClinicalTrials.gov

Outcome 5

FieldValueSource
TypeSECONDARYClinicalTrials.gov
TitleNumber of Participants With First Occurrence of SARS-CoV-2 RT-PCR-Positive Severe COVID-19 in the Initial Vaccination PeriodClinicalTrials.gov
Description
For participants without evidence of infection before vaccination (that is, seronegative and PCR-negative at baseline) who were confirmed to have symptomatic COVID-19, the investigator evaluated if the maximum intensity during the course of the disease met the protocol-specified criteria for severe COVID-19.
ClinicalTrials.gov
Time frameUp to Day 224ClinicalTrials.gov
Population
Modified Intent to Treat (mITT): participants who received at least 1 dose of study drug, excluding participants who had evidence of past or present SARS-CoV-2 infection at baseline. Only data collected during the Initial Vaccination Period reported for this outcome measure.
ClinicalTrials.gov

Trial 8

FieldValueSource
TitleA Study of S-268019 for the Prevention of COVID-19ClinicalTrials.gov
NCT numberNCT05212948ClinicalTrials.gov
PhasesPHASE3ClinicalTrials.gov
ConditionsSARS-CoV-2ClinicalTrials.gov
InterventionsS-268019-b, PlaceboClinicalTrials.gov
Lead sponsorShionogiClinicalTrials.gov
Results first posted2025-11-28ClinicalTrials.gov
Results on ClinicalTrials.govhttps://clinicaltrials.gov/study/NCT05212948?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.