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CVnCoV 12 μg Vaccine vs Placebo: Number of Participants Who Experienced a Fatal SAE

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 10.0005560.000310.000995wilsonClinicalTrials.gov
Risk in group 20.0006080.0003480.00106wilsonClinicalTrials.gov
Risk difference, group 1 minus group 2-0.0000516-0.0005680.000459newcombe hybrid scoreClinicalTrials.gov
Risk ratio, group 1 over group 20.9150.4042.07logClinicalTrials.gov
Odds ratio, group 1 over group 20.9150.4042.07logClinicalTrials.gov
Number needed to treat, for one fewer participant with the outcome on CVnCoV 12 μg Vaccine than on Placebo19,400from the risk difference intervalthe interval includes no differenceClinicalTrials.gov

Groups 2

Group 2 names the comparator: placebo.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov codeSource
Group 1CVnCoV 12 μg VaccineParticipants in the Phase 2b and Phase 3 periods were vaccinated with CVnCoV 12 μg as an intramuscular injection by needle in the deltoid area, preferably in the non-dominant arm, on Day 1 and Day 29.1119,787OG000ClinicalTrials.gov
Group 2Placebo
Participants in the Phase 2b and Phase 3 periods were vaccinated with matching placebo as an intramuscular injection by needle in the deltoid area, preferably in the non-dominant arm, on Day 1 and Day 29.
1219,753OG001ClinicalTrials.gov

Outcome 5

FieldValueSource
TypePRIMARYClinicalTrials.gov
TitleNumber of Participants Who Experienced a Fatal SAEClinicalTrials.gov
Description
A fatal SAE was defined as an SAE that resulted in death.~Participants were censored at the first day after unblinding or at the day after receiving the authorized/licensed vaccine, whichever was earlier.
ClinicalTrials.gov
Time frameDay 1 to Day 393ClinicalTrials.gov
PopulationSAS: Included all participants randomized in Phase 2b or 3 who received at least one dose of CVnCoV or placebo.ClinicalTrials.gov

Trial 8

FieldValueSource
Title
A Phase 2b/3, Randomized, Observer-Blinded, Placebo-Controlled, Multicenter Clinical Study Evaluating the Efficacy and Safety of Investigational SARS-CoV-2 mRNA Vaccine CVnCoV in Adults 18 Years of Age and Older
ClinicalTrials.gov
NCT numberNCT04652102ClinicalTrials.gov
PhasesPHASE2, PHASE3ClinicalTrials.gov
ConditionsCovid19, SARS-CoV-2ClinicalTrials.gov
InterventionsCVnCoV, Placebo, Authorized/licensed vaccines for preventing COVID-19 (AV) as standard of care through their national vaccination programClinicalTrials.gov
Lead sponsorCureVacClinicalTrials.gov
Results first posted2024-04-29ClinicalTrials.gov
Results on ClinicalTrials.govhttps://clinicaltrials.gov/study/NCT04652102?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.