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Trial · NCT00661141

Results by group240

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

OutcomeGroupCategoryValueSpreadUnits
Number of Participants With Adverse Events (AEs), Serious AEs, and AEs Leading to Study DiscontinuationAntizol 1.0 mg/kgAny AE13Participants
Number of Participants With Adverse Events (AEs), Serious AEs, and AEs Leading to Study DiscontinuationAntizol 3.0 mg/kgAny AE6Participants
Number of Participants With Adverse Events (AEs), Serious AEs, and AEs Leading to Study DiscontinuationAntizol 5.0 mg/kgAny AE8Participants
Number of Participants With Adverse Events (AEs), Serious AEs, and AEs Leading to Study DiscontinuationPooled PlaceboAny AE21Participants
Number of Participants With Adverse Events (AEs), Serious AEs, and AEs Leading to Study DiscontinuationOverallAny AE28Participants
Number of Participants With Adverse Events (AEs), Serious AEs, and AEs Leading to Study DiscontinuationAntizol 1.0 mg/kgMild AE13Participants
Number of Participants With Adverse Events (AEs), Serious AEs, and AEs Leading to Study DiscontinuationAntizol 3.0 mg/kgMild AE6Participants
Number of Participants With Adverse Events (AEs), Serious AEs, and AEs Leading to Study DiscontinuationAntizol 5.0 mg/kgMild AE8Participants
Number of Participants With Adverse Events (AEs), Serious AEs, and AEs Leading to Study DiscontinuationPooled PlaceboMild AE19Participants
Number of Participants With Adverse Events (AEs), Serious AEs, and AEs Leading to Study DiscontinuationOverallMild AE28Participants
Number of Participants With Adverse Events (AEs), Serious AEs, and AEs Leading to Study DiscontinuationAntizol 1.0 mg/kgModerate AE2Participants
Number of Participants With Adverse Events (AEs), Serious AEs, and AEs Leading to Study DiscontinuationAntizol 3.0 mg/kgModerate AE0Participants
Number of Participants With Adverse Events (AEs), Serious AEs, and AEs Leading to Study DiscontinuationAntizol 5.0 mg/kgModerate AE0Participants
Number of Participants With Adverse Events (AEs), Serious AEs, and AEs Leading to Study DiscontinuationPooled PlaceboModerate AE5Participants
Number of Participants With Adverse Events (AEs), Serious AEs, and AEs Leading to Study DiscontinuationOverallModerate AE7Participants
Number of Participants With Adverse Events (AEs), Serious AEs, and AEs Leading to Study DiscontinuationAntizol 1.0 mg/kgSevere AE0Participants
Number of Participants With Adverse Events (AEs), Serious AEs, and AEs Leading to Study DiscontinuationAntizol 3.0 mg/kgSevere AE0Participants
Number of Participants With Adverse Events (AEs), Serious AEs, and AEs Leading to Study DiscontinuationAntizol 5.0 mg/kgSevere AE0Participants
Number of Participants With Adverse Events (AEs), Serious AEs, and AEs Leading to Study DiscontinuationPooled PlaceboSevere AE0Participants
Number of Participants With Adverse Events (AEs), Serious AEs, and AEs Leading to Study DiscontinuationOverallSevere AE0Participants

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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