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Trial · NCT03126227

Results by group114

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

OutcomeGroupCategoryValueSpreadUnits
Frequency of Treatment Emergent Adverse Events, Including Serious Adverse EventsAR101 Powder Provided in CapsulesSubjects with at least 1 AE334Participants
Frequency of Treatment Emergent Adverse Events, Including Serious Adverse EventsPlacebo PowderSubjects with at least 1 AE159Participants
Frequency of Treatment Emergent Adverse Events, Including Serious Adverse EventsAR101 Powder Provided in CapsulesMild AE171Participants
Frequency of Treatment Emergent Adverse Events, Including Serious Adverse EventsPlacebo PowderMild AE110Participants
Frequency of Treatment Emergent Adverse Events, Including Serious Adverse EventsAR101 Powder Provided in CapsulesModerate AE151Participants
Frequency of Treatment Emergent Adverse Events, Including Serious Adverse EventsPlacebo PowderModerate AE47Participants
Frequency of Treatment Emergent Adverse Events, Including Serious Adverse EventsAR101 Powder Provided in CapsulesSevere AE11Participants
Frequency of Treatment Emergent Adverse Events, Including Serious Adverse EventsPlacebo PowderSevere AE1Participants
Frequency of Treatment Emergent Adverse Events, Including Serious Adverse EventsAR101 Powder Provided in CapsulesLife Threatening AE1Participants
Frequency of Treatment Emergent Adverse Events, Including Serious Adverse EventsPlacebo PowderLife Threatening AE0Participants
Frequency of Treatment Emergent Adverse Events, Including Serious Adverse EventsAR101 Powder Provided in CapsulesDeath0Participants
Frequency of Treatment Emergent Adverse Events, Including Serious Adverse EventsPlacebo PowderDeath1Participants
Frequency of Treatment Emergent Adverse Events, Including Serious Adverse EventsAR101 Powder Provided in CapsulesSubjects with at least 1 serious adverse event2Participants
Frequency of Treatment Emergent Adverse Events, Including Serious Adverse EventsPlacebo PowderSubjects with at least 1 serious adverse event2Participants
Frequency of Premature Discontinuation of Dosing Due to Adverse EventsAR101 Powder Provided in Capsules41Participants
Frequency of Premature Discontinuation of Dosing Due to Adverse EventsPlacebo Powder5Participants
Frequency of Premature Discontinuation of Dosing Due to Chronic/Recurrent Gastrointestinal Adverse EventsAR101 Powder Provided in Capsules20Participants
Frequency of Premature Discontinuation of Dosing Due to Chronic/Recurrent Gastrointestinal Adverse EventsPlacebo Powder0Participants
Proportion of Chronic/Recurrent Gastrointestinal Adverse Events Resolving <2, Between 2-4, Between 4-12, and ≥ 12 Weeks Following Discontinuation of DosingAR101 Powder Provided in Capsules< 2 weeks17Participants
Proportion of Chronic/Recurrent Gastrointestinal Adverse Events Resolving <2, Between 2-4, Between 4-12, and ≥ 12 Weeks Following Discontinuation of DosingPlacebo Powder< 2 weeks0Participants

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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