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Trial · NCT02439320

Outcomes12

Each outcome the trial posted results for, in ClinicalTrials.gov's words.

TypeOutcomeTime framePopulationUnitsMeasured as
PRIMARYPercentage of Participants Who Are Headache Pain Free2 hours post doseAll randomized participants who received at least one dose of study drug and had evaluable headache pain free data.percentage of participantsNUMBER
PRIMARYPercentage of Participants Who Are Most Bothersome Symptom (MBS) Free2 hours post doseAll randomized participants who received at least one dose of study drug and had evaluable MBS data.percentage of participantsNUMBER
SECONDARYPercentage of Participants Who Have Headache Relief After First Dose2 hours post doseAll randomized participants who received at least one dose of study drug and had evaluable headache relief data.percentage of participantsNUMBER
SECONDARYPercentage of Participants With Headache RecurrenceFrom 2 hours post dose up to 48 hoursRandomized participants who received a dose of study drug and had postdose headache severity or symptom assessments.percentage of participantsNUMBER
SECONDARYPercentage of Participants Who Used Rescue Medication2 hours post doseRandomized participants who received a dose of study drug and had postdose headache severity or symptom assessments.percentage of participantsNUMBER
SECONDARYPercentage of Participants Who Used Rescue MedicationAnytime between 2-24 hours post doseRandomized participants who received a dose of study drug and had postdose headache severity or symptom assessments.percentage of participantsNUMBER
SECONDARYPercentage of Participants Who Used Rescue MedicationAnytime 24-48 hours post doseAll randomized participants who received at least one dose of study drug and had evaluable use of rescue medication data.percentage of participantsNUMBER
SECONDARYPercentage of Participants Nausea Free2 hours post doseAll randomized participants who used at least 1 dose of study drug and had any post-dose headache severity or symptom assessments.percentage of participantsNUMBER
SECONDARYPercentage of Participants Phonophobia Free2 hours post doseAll randomized participants who used at least 1 dose of study drug and had any post-dose headache severity or symptom assessments.percentage of participantsNUMBER
SECONDARYPercentage of Participants Photophobia Free2 hours post doseAll randomized participants who received at least one dose of study drug and had evaluable photophobia free data.percentage of participantsNUMBER
SECONDARYParticipants With Serious Adverse Events (SAE)Baseline up to 11 weeksAll randomized participants who had received at least one dose of study drug. Results are displayed by the first dose taken.ParticipantsCOUNT_OF_PARTICIPANTS
OTHER_PRE_SPECIFIEDPercentage of Participants With Resource Utilization6 months prior to enrolling in study to end of study (Up to 11 Weeks) within 7 days of treating a single migraine attackAll randomized participants who used at least 1 dose of study drug, regardless of whether or not they underwent any study assessments.percentage of participantsNUMBER

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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