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M-001 vs Saline: Number of Participants With Influenza-like Illness Symptoms

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 10.210.20.221wilsonClinicalTrials.gov
Risk in group 20.2140.2040.225wilsonClinicalTrials.gov
Risk difference, group 1 minus group 2-0.00447-0.01920.0103newcombe hybrid scoreClinicalTrials.gov
Risk ratio, group 1 over group 20.9790.9131.05logClinicalTrials.gov
Odds ratio, group 1 over group 20.9740.8911.06logClinicalTrials.gov
Number needed to treat, for one fewer participant with the outcome on M-001 than on Saline224from 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 1M-001
Participants will be vaccinated with 1mg dose of M-001 twice: Once at Day 0, and once at Day 21.~M-001: A recombinant protein containing 9 conserved epitopes from Influenza A and B that are common to the vast majority of influenza viruses.
1,2315,864OG000ClinicalTrials.gov
Group 2SalineParticipants will be vaccinated with saline twice: Once at Day 0, and once at Day 21.~Saline: 0.9% sodium chloride (NaCl)1,2665,905OG001ClinicalTrials.gov

Outcome 5

FieldValueSource
TypeSECONDARYClinicalTrials.gov
TitleNumber of Participants With Influenza-like Illness SymptomsClinicalTrials.gov
DescriptionAssessment of number of participants having ILI symptoms in the experimental or control groupClinicalTrials.gov
Time frameFrom Day 14 post-second vaccination day to end of influenza season, an average of 4 months per participant per yearClinicalTrials.gov
PopulationPer protocol population comprises all subjects who received both doses of vaccine or placebo and had at least one contact with study staff after 15 days or more upon second vaccination.ClinicalTrials.gov

Trial 8

FieldValueSource
TitleA Pivotal Trial to Assess the Safety and Clinical Efficacy of the M-001 as a Standalone Universal Flu VaccineClinicalTrials.gov
NCT numberNCT03450915ClinicalTrials.gov
PhasesPHASE3ClinicalTrials.gov
ConditionsInfluenzaClinicalTrials.gov
InterventionsM-001, SalineClinicalTrials.gov
Lead sponsorBiondVax Pharmaceuticals ltd.ClinicalTrials.gov
Results first posted2021-09-13ClinicalTrials.gov
Results on ClinicalTrials.govhttps://clinicaltrials.gov/study/NCT03450915?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.