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Trial · NCT02075255

Results by group157

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

OutcomeGroupCategoryValueSpreadUnits
Percentage Reduction in Final OCS Dose Compared With Baseline While Maintaining Asthma ControlBenralizumab 30 mg q.4 Weeks75.0095% Confidence Interval 50.00 to 83.30Percent
Percentage Reduction in Final OCS Dose Compared With Baseline While Maintaining Asthma ControlBenralizumab 30 mg q.8 Weeks75.0095% Confidence Interval 60.00 to 87.50Percent
Percentage Reduction in Final OCS Dose Compared With Baseline While Maintaining Asthma ControlPlacebo25.0095% Confidence Interval 0.00 to 33.30Percent
Number and Percentage of Patients in Different Categories of Percent Reduction From Baseline in Final OCS Dose While Maintaining Asthma ControlBenralizumab 30 mg q.4 Weeks>=90% reduction24Participants
Number and Percentage of Patients in Different Categories of Percent Reduction From Baseline in Final OCS Dose While Maintaining Asthma ControlBenralizumab 30 mg q.8 Weeks>=90% reduction27Participants
Number and Percentage of Patients in Different Categories of Percent Reduction From Baseline in Final OCS Dose While Maintaining Asthma ControlPlacebo>=90% reduction9Participants
Number and Percentage of Patients in Different Categories of Percent Reduction From Baseline in Final OCS Dose While Maintaining Asthma ControlBenralizumab 30 mg q.4 Weeks>=75% reduction38Participants
Number and Percentage of Patients in Different Categories of Percent Reduction From Baseline in Final OCS Dose While Maintaining Asthma ControlBenralizumab 30 mg q.8 Weeks>=75% reduction37Participants
Number and Percentage of Patients in Different Categories of Percent Reduction From Baseline in Final OCS Dose While Maintaining Asthma ControlPlacebo>=75% reduction15Participants
Number and Percentage of Patients in Different Categories of Percent Reduction From Baseline in Final OCS Dose While Maintaining Asthma ControlBenralizumab 30 mg q.4 Weeks>=50% reduction48Participants
Number and Percentage of Patients in Different Categories of Percent Reduction From Baseline in Final OCS Dose While Maintaining Asthma ControlBenralizumab 30 mg q.8 Weeks>=50% reduction48Participants
Number and Percentage of Patients in Different Categories of Percent Reduction From Baseline in Final OCS Dose While Maintaining Asthma ControlPlacebo>=50% reduction28Participants
Number and Percentage of Patients in Different Categories of Percent Reduction From Baseline in Final OCS Dose While Maintaining Asthma ControlBenralizumab 30 mg q.4 Weeks>0% reduction55Participants
Number and Percentage of Patients in Different Categories of Percent Reduction From Baseline in Final OCS Dose While Maintaining Asthma ControlBenralizumab 30 mg q.8 Weeks>0% reduction58Participants
Number and Percentage of Patients in Different Categories of Percent Reduction From Baseline in Final OCS Dose While Maintaining Asthma ControlPlacebo>0% reduction40Participants
Number and Percentage of Patients in Different Categories of Percent Reduction From Baseline in Final OCS Dose While Maintaining Asthma ControlBenralizumab 30 mg q.4 WeeksNo change or any increase17Participants
Number and Percentage of Patients in Different Categories of Percent Reduction From Baseline in Final OCS Dose While Maintaining Asthma ControlBenralizumab 30 mg q.8 WeeksNo change or any increase15Participants
Number and Percentage of Patients in Different Categories of Percent Reduction From Baseline in Final OCS Dose While Maintaining Asthma ControlPlaceboNo change or any increase35Participants
Percentage Reduction in Final OCS Dose Compared With Baseline While Maintaining Asthma Control for Patients With Baseline Eosinophils >=300/uLBenralizumab 30 mg q.4 Weeks75.0095% Confidence Interval 60.00 to 100.00Percent
Percentage Reduction in Final OCS Dose Compared With Baseline While Maintaining Asthma Control for Patients With Baseline Eosinophils >=300/uLBenralizumab 30 mg q.8 Weeks75.0095% Confidence Interval 60.00 to 91.70Percent

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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