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Quadrivalent (30 μg) VLP Vaccine vs Active Comparator (Fluarix): Number of Participants Who Withdrew Due to an AE

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 10.002360.001430.00389wilsonClinicalTrials.gov
Risk in group 20.003140.002030.00485wilsonClinicalTrials.gov
Risk difference, group 1 minus group 2-0.00078-0.002720.00111newcombe hybrid scoreClinicalTrials.gov
Risk ratio, group 1 over group 20.7520.3851.47logClinicalTrials.gov
Odds ratio, group 1 over group 20.7510.3841.47logClinicalTrials.gov
Number needed to treat, for one fewer participant with the outcome on Quadrivalent (30 μg) VLP Vaccine than on Active Comparator (Fluarix)1,280from the risk difference intervalthe interval includes no differenceClinicalTrials.gov

Groups 2

Neither group, or both, names a comparator, so the groups keep ClinicalTrials.gov's order.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov codeSource
Group 1Quadrivalent (30 μg) VLP VaccineParticipants received one IM injection of 0.5 mL of 30 μg/strain of the Quadrivalent VLP Influenza Vaccine on Day 0.156,352OG000ClinicalTrials.gov
Group 2Active Comparator (Fluarix)Participants received one IM injection of 0.5 mL of 15 μg/strain of the Fluarix Quadrivalent® comparator vaccine on Day 0.206,366OG001ClinicalTrials.gov

Outcome 5

FieldValueSource
TypeSECONDARYClinicalTrials.gov
TitleNumber of Participants Who Withdrew Due to an AEClinicalTrials.gov
Description
An AE or adverse experience was defined as any untoward medical occurrence in a participant or clinical investigation participant who received study drug, with or without a causal relationship with the treatment. An AE can be any favorable and unintended sign, symptom, or disease temporally associated with the use of a medicinal product, whether or not related to a medicinal product.
ClinicalTrials.gov
Time frameDay 0 up to ~9 monthsClinicalTrials.gov
PopulationSAS. Participants that were non-compliant to protocol/GCP, as per investigator, were excluded from analysis.ClinicalTrials.gov

Trial 8

FieldValueSource
TitleEfficacy of a Plant-derived Quadrivalent Virus-like Particle (VLP) Vaccine in the ElderlyClinicalTrials.gov
NCT numberNCT03739112ClinicalTrials.gov
PhasesPHASE3ClinicalTrials.gov
ConditionsVirus Diseases, RNA Virus Infections, Respiratory Tract Diseases, Respiratory Tract InfectionsClinicalTrials.gov
InterventionsQuadrivalent VLP Vaccine, Fluarix Quadrivalent® Comparator VaccineClinicalTrials.gov
Lead sponsorMedicagoClinicalTrials.gov
Results first posted2023-06-23ClinicalTrials.gov
Results on ClinicalTrials.govhttps://clinicaltrials.gov/study/NCT03739112?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.