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Trial · NCT02485301

Results by group399

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

OutcomeGroupCategoryValueSpreadUnits
Number of Subjects With Solicited Local Adverse EventsGSK3390107A GroupAny Pain356Participants
Number of Subjects With Solicited Local Adverse EventsPlacebo+GSK3390107A GroupAny Pain57Participants
Number of Subjects With Solicited Local Adverse EventsGSK3390107A GroupGrade 3 Pain3Participants
Number of Subjects With Solicited Local Adverse EventsPlacebo+GSK3390107A GroupGrade 3 Pain0Participants
Number of Subjects With Solicited Local Adverse EventsGSK3390107A GroupAny Redness2Participants
Number of Subjects With Solicited Local Adverse EventsPlacebo+GSK3390107A GroupAny Redness0Participants
Number of Subjects With Solicited Local Adverse EventsGSK3390107A GroupGrade 3 Redness0Participants
Number of Subjects With Solicited Local Adverse EventsPlacebo+GSK3390107A GroupGrade 3 Redness0Participants
Number of Subjects With Solicited Local Adverse EventsGSK3390107A GroupAny Swelling9Participants
Number of Subjects With Solicited Local Adverse EventsPlacebo+GSK3390107A GroupAny Swelling5Participants
Number of Subjects With Solicited Local Adverse EventsGSK3390107A GroupGrade 3 Swelling0Participants
Number of Subjects With Solicited Local Adverse EventsPlacebo+GSK3390107A GroupGrade 3 Swelling0Participants
Number of Subjects With Solicited General Adverse EventsGSK3390107A GroupAny Fatigue284Participants
Number of Subjects With Solicited General Adverse EventsPlacebo+GSK3390107A GroupAny Fatigue94Participants
Number of Subjects With Solicited General Adverse EventsGSK3390107A GroupGrade 3 Fatigue11Participants
Number of Subjects With Solicited General Adverse EventsPlacebo+GSK3390107A GroupGrade 3 Fatigue3Participants
Number of Subjects With Solicited General Adverse EventsGSK3390107A GroupRelated Fatigue243Participants
Number of Subjects With Solicited General Adverse EventsPlacebo+GSK3390107A GroupRelated Fatigue72Participants
Number of Subjects With Solicited General Adverse EventsGSK3390107A GroupAny Fever106Participants
Number of Subjects With Solicited General Adverse EventsPlacebo+GSK3390107A GroupAny Fever24Participants

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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