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Trial · NCT03557307

Results by group28

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

OutcomeGroupCategoryValueSpreadUnits
Patients Who Achieve 100% Reduction in Daily OCS DoseBenra 30 mg376Participants
Patients Who Achieve 100% Reduction or a Daily OCS Dose of <=5mgBenra 30 mg490Participants
Patients Who Achieve a Daily OCS of ≤5mgBenra 30 mg547Participants
Patients Who Achieve a ≥90%, ≥75%, and ≥50% Reduction in Daily OCS DoseBenra 30 mg≥90% reduction383Participants
Patients Who Achieve a ≥90%, ≥75%, and ≥50% Reduction in Daily OCS DoseBenra 30 mg≥75% reduction412Participants
Patients Who Achieve a ≥90%, ≥75%, and ≥50% Reduction in Daily OCS DoseBenra 30 mg≥50% reduction489Participants
Change From Baseline in Average Daily OCS Dose (mg)Benra 30 mg-8.5095% Confidence Interval -9.10 to -7.90mg
Patients Who Achieve 100% Reduction in Daily OCS Dose From Main Study Baseline OCS Dose to the End of the Long Term Follow up SubstudyAsthma Treatment as Per Healthcare Provider Discretion138Participants
Patients Who Achieve 100% Reduction in Daily OCS Dose From Main Study Baseline OCS Dose to the End of the Long Term Follow up Substudy>=50% Any Biologic60Participants
Patients Who Achieve 100% Reduction in Daily OCS Dose From Main Study Baseline OCS Dose to the End of the Long Term Follow up Substudy>=50% Benra54Participants
Patients Who Achieve a Daily OCS Dose of ≤5 mg at the End of the Long Term Follow up SubstudyAsthma Treatment as Per Healthcare Provider Discretion177Participants
Patients Who Achieve a Daily OCS Dose of ≤5 mg at the End of the Long Term Follow up Substudy>=50% Any Biologic72Participants
Patients Who Achieve a Daily OCS Dose of ≤5 mg at the End of the Long Term Follow up Substudy>=50% Benra65Participants
Patients Who Achieve ≥90%, ≥75%, ≥50% or >0% OCS Reduction From Main Study Baseline OCS Dose to the End of the Long Term Follow up SubstudyAsthma Treatment as Per Healthcare Provider Discretion>=90% reduction141Participants
Patients Who Achieve ≥90%, ≥75%, ≥50% or >0% OCS Reduction From Main Study Baseline OCS Dose to the End of the Long Term Follow up Substudy>=50% Any Biologic>=90% reduction61Participants
Patients Who Achieve ≥90%, ≥75%, ≥50% or >0% OCS Reduction From Main Study Baseline OCS Dose to the End of the Long Term Follow up Substudy>=50% Benra>=90% reduction55Participants
Patients Who Achieve ≥90%, ≥75%, ≥50% or >0% OCS Reduction From Main Study Baseline OCS Dose to the End of the Long Term Follow up SubstudyAsthma Treatment as Per Healthcare Provider Discretion>=75% reduction151Participants
Patients Who Achieve ≥90%, ≥75%, ≥50% or >0% OCS Reduction From Main Study Baseline OCS Dose to the End of the Long Term Follow up Substudy>=50% Any Biologic>=75% reduction64Participants
Patients Who Achieve ≥90%, ≥75%, ≥50% or >0% OCS Reduction From Main Study Baseline OCS Dose to the End of the Long Term Follow up Substudy>=50% Benra>=75% reduction58Participants
Patients Who Achieve ≥90%, ≥75%, ≥50% or >0% OCS Reduction From Main Study Baseline OCS Dose to the End of the Long Term Follow up SubstudyAsthma Treatment as Per Healthcare Provider Discretion>=50% reduction172Participants

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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