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D-QIV vs Control: Number of Subjects With First Occurrence of Culture-confirmed Moderate to Severe Influenza A and/or B Disease Due to Any Seasonal Influenza Strain.

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 10.01380.01110.0172wilsonClinicalTrials.gov
Risk in group 20.03790.03330.0432wilsonClinicalTrials.gov
Risk difference, group 1 minus group 2-0.0241-0.03-0.0183newcombe hybrid scoreClinicalTrials.gov
Risk ratio, group 1 over group 20.3650.2830.471logClinicalTrials.gov
Odds ratio, group 1 over group 20.3560.2750.462logClinicalTrials.gov
Number needed to treat, for one fewer participant with the outcome on D-QIV than on Control41.533.354.6from the risk difference intervalClinicalTrials.gov

Groups 2

Group 2 names the comparator: control.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov codeSource
Group 1D-QIVSubjects received 1 or 2 doses of candidate influenza Influsplit™ Tetra vaccine (GSK2321138A).795,707OG000ClinicalTrials.gov
Group 2ControlIn function of their age and Influsplit™ Tetra (D-QIV) vaccine status, subjects received Prevenar 13® or Havrix® Junior and possibly a varicella vaccine (Varilrix® or Varivax/ProVarivax ®).2165,697OG001ClinicalTrials.gov

Outcome 5

FieldValueSource
TypeSECONDARYClinicalTrials.gov
TitleNumber of Subjects With First Occurrence of Culture-confirmed Moderate to Severe Influenza A and/or B Disease Due to Any Seasonal Influenza Strain.ClinicalTrials.gov
DescriptionAttack rate (AR) was defined as the number/percentage of subjects with at least 1 RT-PCR confirmed influenza event.ClinicalTrials.gov
Time frameDuring the surveillance period (approximately 6 to 8 months)ClinicalTrials.gov
Population
The ATP cohort for efficacy - Time to event included all eligible subjects who received study vaccine(s) according to their random assignment, for whom vaccine administration site was known, who had a swab collected during the window (0-7 days) of episode onset and who would be censored but not eliminated based on protocol criteria.
ClinicalTrials.gov

Trial 8

FieldValueSource
TitleAn Efficacy Study of GlaxoSmithKline (GSK) Biologicals' Candidate Influenza Vaccine GSK2321138A in ChildrenClinicalTrials.gov
NCT numberNCT01439360ClinicalTrials.gov
PhasesPHASE3ClinicalTrials.gov
ConditionsInfluenzaClinicalTrials.gov
InterventionsQuadrivalent seasonal influenza vaccine(Flu D-QIV) GSK2321138A, Havrix Junior, Prevenar 13, Varivax/ProVarivax, VarilrixClinicalTrials.gov
Lead sponsorGlaxoSmithKlineClinicalTrials.gov
Results first posted2017-03-08ClinicalTrials.gov
Results on ClinicalTrials.govhttps://clinicaltrials.gov/study/NCT01439360?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.