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Trial · NCT03240133

Results by group18

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

OutcomeGroupCategoryValueSpreadUnits
Proportion of Subjects With Improved or Stable Composite Visual Analog Scale (VAS) ScorePart 1: Berotralstat 750 mg - Predose13.96Standard Deviation 9.84VAS score - millimeters
Proportion of Subjects With Improved or Stable Composite Visual Analog Scale (VAS) ScorePart 1: Placebo - Pre-dose15.04Standard Deviation 11.90VAS score - millimeters
Proportion of Subjects With Improved or Stable Composite Visual Analog Scale (VAS) ScorePart 1: Berotralstat 750 mg - 4hr Post-dose10.54Standard Deviation 11.39VAS score - millimeters
Proportion of Subjects With Improved or Stable Composite Visual Analog Scale (VAS) ScorePart 1: Placebo - 4hr Post-dose18.42Standard Deviation 14.19VAS score - millimeters
Proportion of Subjects With Improved or Stable Composite Visual Analog Scale (VAS) ScorePart 2: Berotralstat 500 mg - Predose17.69Standard Deviation 15.25VAS score - millimeters
Proportion of Subjects With Improved or Stable Composite Visual Analog Scale (VAS) ScorePart 2: Placebo - Pre-dose13.48Standard Deviation 16.11VAS score - millimeters
Proportion of Subjects With Improved or Stable Composite Visual Analog Scale (VAS) ScorePart 2: Berotralstat 500 mg - 4hr Post-dose11.31Standard Deviation 15.75VAS score - millimeters
Proportion of Subjects With Improved or Stable Composite Visual Analog Scale (VAS) ScorePart 2: Placebo - 4hr Post-dose9.26Standard Deviation 11.53VAS score - millimeters
Proportion of Subjects With Improved or Stable Composite Visual Analog Scale (VAS) ScorePart 3: Berotralstat 250 mg - Predose14.57Standard Deviation 11.78VAS score - millimeters
Proportion of Subjects With Improved or Stable Composite Visual Analog Scale (VAS) ScorePart 3: Placebo - Pre-dose11.33Standard Deviation 10.17VAS score - millimeters
Proportion of Subjects With Improved or Stable Composite Visual Analog Scale (VAS) ScorePart 3: Berotralstat 250 mg - 4hr Post-dose10.92Standard Deviation 10.31VAS score - millimeters
Proportion of Subjects With Improved or Stable Composite Visual Analog Scale (VAS) ScorePart 3: Placebo - 4hr Post-dose9.21Standard Deviation 9.67VAS score - millimeters
Percentage of Attacks Treated With Standard of Care Acute Attack Medication (SOC-Rx) Through 24 HoursPart 1: Berotralstat 750 mg29.7Percentage attacks treated with SOC-Rx
Percentage of Attacks Treated With Standard of Care Acute Attack Medication (SOC-Rx) Through 24 HoursPart 1: Placebo61.3Percentage attacks treated with SOC-Rx
Percentage of Attacks Treated With Standard of Care Acute Attack Medication (SOC-Rx) Through 24 HoursPart 2: Berotralstat 500 mg32.0Percentage attacks treated with SOC-Rx
Percentage of Attacks Treated With Standard of Care Acute Attack Medication (SOC-Rx) Through 24 HoursPart 2: Placebo45.5Percentage attacks treated with SOC-Rx
Percentage of Attacks Treated With Standard of Care Acute Attack Medication (SOC-Rx) Through 24 HoursPart 3: Berotralstat 250 mg38.1Percentage attacks treated with SOC-Rx
Percentage of Attacks Treated With Standard of Care Acute Attack Medication (SOC-Rx) Through 24 HoursPart 3: Placebo45.5Percentage attacks treated with SOC-Rx

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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