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Trial · NCT04498832

Results by group114

Each measurement the trial posted, group by group, in the words and numbers it posted.

OutcomeGroupCategoryValueSpreadUnits
Geometric Mean Titers (GMTs) of Influenza Vaccine Antibodies at Day 28QIV-HDA/H1N1309.095% Confidence Interval 282.1 to 338.4titers
Geometric Mean Titers (GMTs) of Influenza Vaccine Antibodies at Day 28QIV-SDA/H1N1110.095% Confidence Interval 100.0 to 121.1titers
Geometric Mean Titers (GMTs) of Influenza Vaccine Antibodies at Day 28QIV-HDA/H3N2-like540.095% Confidence Interval 504.4 to 578.0titers
Geometric Mean Titers (GMTs) of Influenza Vaccine Antibodies at Day 28QIV-SDA/H3N2-like239.995% Confidence Interval 222.0 to 259.1titers
Geometric Mean Titers (GMTs) of Influenza Vaccine Antibodies at Day 28QIV-HDB/Victoria-like354.895% Confidence Interval 333.0 to 378.0titers
Geometric Mean Titers (GMTs) of Influenza Vaccine Antibodies at Day 28QIV-SDB/Victoria-like139.295% Confidence Interval 129.4 to 149.8titers
Geometric Mean Titers (GMTs) of Influenza Vaccine Antibodies at Day 28QIV-HDB/Yamagata795.895% Confidence Interval 750.3 to 844.1titers
Geometric Mean Titers (GMTs) of Influenza Vaccine Antibodies at Day 28QIV-SDB/Yamagata254.795% Confidence Interval 237.7 to 273.0titers
Percentage of Participants Achieving Seroconversion Against Influenza Virus Antigens: Superiority AnalysisQIV-HDA/H1N177.695% Confidence Interval 75.0 to 80.1percentage of participants
Percentage of Participants Achieving Seroconversion Against Influenza Virus Antigens: Superiority AnalysisQIV-SDA/H1N147.995% Confidence Interval 44.9 to 51.0percentage of participants
Percentage of Participants Achieving Seroconversion Against Influenza Virus Antigens: Superiority AnalysisQIV-HDA/H3N2-like75.495% Confidence Interval 72.6 to 77.9percentage of participants
Percentage of Participants Achieving Seroconversion Against Influenza Virus Antigens: Superiority AnalysisQIV-SDA/H3N2-like47.395% Confidence Interval 44.2 to 50.4percentage of participants
Percentage of Participants Achieving Seroconversion Against Influenza Virus Antigens: Superiority AnalysisQIV-HDB/Victoria-like79.295% Confidence Interval 76.6 to 81.6percentage of participants
Percentage of Participants Achieving Seroconversion Against Influenza Virus Antigens: Superiority AnalysisQIV-SDB/Victoria-like47.895% Confidence Interval 44.7 to 50.8percentage of participants
Percentage of Participants Achieving Seroconversion Against Influenza Virus Antigens: Superiority AnalysisQIV-HDB/Yamagata74.495% Confidence Interval 71.7 to 77.1percentage of participants
Percentage of Participants Achieving Seroconversion Against Influenza Virus Antigens: Superiority AnalysisQIV-SDB/Yamagata39.095% Confidence Interval 36.1 to 42.1percentage of participants
GMTs of Influenza Vaccine Antibodies at Day 0 and Day 28QIV-HDA/H1N1: Day 014.595% Confidence Interval 13.5 to 15.5titers
GMTs of Influenza Vaccine Antibodies at Day 0 and Day 28QIV-SDA/H1N1: Day 014.995% Confidence Interval 13.9 to 16.1titers
GMTs of Influenza Vaccine Antibodies at Day 0 and Day 28QIV-HDA/H1N1: Day 28309.095% Confidence Interval 282.1 to 338.4titers
GMTs of Influenza Vaccine Antibodies at Day 0 and Day 28QIV-SDA/H1N1: Day 28110.095% Confidence Interval 100.0 to 121.1titers

Source ClinicalTrials.govtrials-2026-11-12-0.5.0

Sources 3

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNo license stated
  • NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
  • ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.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.govnone stated
  • NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

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