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Trial · NCT05281094

Results by group70

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

OutcomeGroupCategoryValueSpreadUnits
To Demonstrate the Efficacy of HIL-214 Vaccine Against Moderate/Severe Acute Gastroenteritis (AGE) Associated Only With GI.1 or GII.4 Norovirus Genotypes.Placebo3.07Standard Deviation 2.059months
To Demonstrate the Efficacy of HIL-214 Vaccine Against Moderate/Severe Acute Gastroenteritis (AGE) Associated Only With GI.1 or GII.4 Norovirus Genotypes.Experimental3.29Standard Deviation 1.746months
To Evaluate the Efficacy of HIL-214 Vaccine Against Moderate/Severe Acute Gastroenteritis (AGE) Associated Only With Any Norovirus (GI or GII) Genogroup.Placebo3.16Standard Deviation 1.886months
To Evaluate the Efficacy of HIL-214 Vaccine Against Moderate/Severe Acute Gastroenteritis (AGE) Associated Only With Any Norovirus (GI or GII) Genogroup.Experimental3.32Standard Deviation 1.519months
To Evaluate the Efficacy of HIL-214 Vaccine Against Moderate/Severe Acute Gastroenteritis (AGE) Associated With GI.1 or GII.4 Norovirus Genotypes, Irrespective of Other Gastrointestinal Pathogens.Placebo3.11Standard Deviation 1.981months
To Evaluate the Efficacy of HIL-214 Vaccine Against Moderate/Severe Acute Gastroenteritis (AGE) Associated With GI.1 or GII.4 Norovirus Genotypes, Irrespective of Other Gastrointestinal Pathogens.Experimental3.29Standard Deviation 1.628months
To Evaluate the Efficacy of HIL-214 Vaccine Against Moderate/Severe Acute Gastroenteritis (AGE) Associated With Any Norovirus Genogroup (GI or GII), Irrespective of Other Gastrointestinal PathogensPlacebo3.19Standard Deviation 1.852months
To Evaluate the Efficacy of HIL-214 Vaccine Against Moderate/Severe Acute Gastroenteritis (AGE) Associated With Any Norovirus Genogroup (GI or GII), Irrespective of Other Gastrointestinal PathogensExperimental3.17Standard Deviation 1.541months
Immunogenicity of HIL-214 Compared to PlaceboPlaceboAnti-GI.1 HBGA-blocking seroresponse rate at Visit 20.695% Confidence Interval 0.3 to 1.2percentage of participants
Immunogenicity of HIL-214 Compared to PlaceboExperimentalAnti-GI.1 HBGA-blocking seroresponse rate at Visit 236.895% Confidence Interval 34.3 to 39.4percentage of participants
Immunogenicity of HIL-214 Compared to PlaceboPlaceboAnti-GI.1 HBGA-blocking seroresponse rate at Visit 31.495% Confidence Interval 0.8 to 2.1percentage of participants
Immunogenicity of HIL-214 Compared to PlaceboExperimentalAnti-GI.1 HBGA-blocking seroresponse rate at Visit 395.595% Confidence Interval 94.3 to 96.6percentage of participants
Immunogenicity of HIL-214 Compared to PlaceboPlaceboAnti-GI.1 HBGA-blocking seroresponse rate at Visit 41.695% Confidence Interval 1.0 to 2.4percentage of participants
Immunogenicity of HIL-214 Compared to PlaceboExperimentalAnti-GI.1 HBGA-blocking seroresponse rate at Visit 486.295% Confidence Interval 84.3 to 88.0percentage of participants
Immunogenicity of HIL-214 Compared to PlaceboPlaceboAnti-GII.4c HBGA-blocking seroresponse rate at Visit 21.395% Confidence Interval 0.8 to 2.1percentage of participants
Immunogenicity of HIL-214 Compared to PlaceboExperimentalAnti-GII.4c HBGA-blocking seroresponse rate at Visit 27.495% Confidence Interval 6.1 to 8.9percentage of participants
Immunogenicity of HIL-214 Compared to PlaceboPlaceboAnti- GII.4c HBGA-blocking seroresponse rate at Visit 32.295% Confidence Interval 1.5 to 3.2percentage of participants
Immunogenicity of HIL-214 Compared to PlaceboExperimentalAnti- GII.4c HBGA-blocking seroresponse rate at Visit 343.095% Confidence Interval 40.4 to 45.6percentage of participants
Immunogenicity of HIL-214 Compared to PlaceboPlaceboAnti- GII.4c HBGA-blocking seroresponse rate at Visit 46.295% Confidence Interval 5.0 to 7.6percentage of participants
Immunogenicity of HIL-214 Compared to PlaceboExperimentalAnti- GII.4c HBGA-blocking seroresponse rate at Visit 425.095% Confidence Interval 22.8 to 27.4percentage of participants

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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