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Trial · NCT01264939

Outcomes11

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

TypeOutcomeTime framePopulationUnitsMeasured as
SECONDARYChange From Baseline to Week 12 in the Weekly Itch Severity ScoreBaseline to Week 12Modified intent-to-treat population: All randomized patients who received at least 1 dose of study drug.Units on a scaleMEAN
SECONDARYChange From Baseline to Week 12 in the Urticaria Activity Score Over 7 Days (UAS7)Baseline to Week 12Modified intent-to-treat population: All randomized patients who received at least 1 dose of study drug.Units on a scaleMEAN
SECONDARYChange From Baseline to Week 12 in the Weekly Number of Hives ScoreBaseline to Week 12Modified intent-to-treat population: All randomized patients who received at least 1 dose of study drug.Units on a scaleMEAN
SECONDARYTime to Minimally Important Difference (MID) Response in the Weekly Itch Severity Score by Week 12Baseline to Week 12Modified intent-to-treat population: All randomized patients who received at least 1 dose of study drug. Only patients with a MID response were included in the analysis.WeeksMEDIAN
SECONDARYPercentage of Participants With a UAS7 Score ≤ 6 at Week 12Week 12Modified intent-to-treat population: All randomized patients who received at least 1 dose of study drug.Percentage of participantsNUMBER
SECONDARYPercentage of Weekly Itch Severity Score MID Responders at Week 12Baseline to Week 12Modified intent-to-treat population: All randomized patients who received at least 1 dose of study drug.Percentage of participantsNUMBER
SECONDARYChange From Baseline to Week 12 in the Weekly Size of the Largest Hive ScoreBaseline to Week 12Modified intent-to-treat population: All randomized patients who received at least 1 dose of study drug.Units on a scaleMEAN
SECONDARYChange From Baseline in the Overall Dermatology Life Quality Index (DLQI) Score at Week 12Baseline to Week 12Modified intent-to-treat population: All randomized patients who received at least 1 dose of study drug and who had a DLQI score at Week 12.Units on a scaleMEAN
SECONDARYPercentage of Angioedema-free Days From Week 4 to Week 12Week 4 to Week 12
Modified intent-to-treat population: All randomized patients who received at least 1 dose of study drug. Patients who withdrew before the Week 4 visit or who had missing responses for more than 40% of the daily diary entries between the Week 4 visit and the Week 12 visit were not included in the analysis.
Percentage of daysMEAN
SECONDARYPercentage of Complete Responders (UAS7 = 0) at Week 12Week 12Modified intent-to-treat population: All randomized patients who received at least 1 dose of study drug.Percentage of participantsNUMBER
PRIMARYPercentage of Participants With Adverse EventsBaseline to the end of study (up to 40 weeks)Safety population: All randomized participants who received at least 1 dose of study drug.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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GET https://conductscience.org/api/trials/v1/NCT01264939/outcomes