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Trial · NCT02869438

Outcomes23

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

TypeOutcomeTime framePopulationUnitsMeasured as
PRIMARYChange From Baseline (Visit 4) to Day 28 (Visit 8), Day 56 (Visit 9), and Day 84 (Visit 10) in Pre-BD FEV1From first IP dose to Day 84Full analysis setLiterMEAN
PRIMARYChange From Baseline (Visit 4) to End of Treatment Day 84 (Visit 10) in Residual Volume (RV)From first IP dose to Day 84Body plethysmography sub-study analysis setLiterMEAN
SECONDARYPercent Change From Baseline to End of Treatment in Eosinophils CountsFrom first IP dose to Day 84Full analysis setPercent changeMEAN
SECONDARYChange From Baseline (Visit 4) to Post Baseline Visits in Pre-BD FEV1From first IP dose to Day 84Full analysis setLiterMEAN
SECONDARYChange From Baseline to Post Baseline for Pre-BD FVCFrom first IP dose to Day 84Full analysis setLiterMEAN
SECONDARYPercentage of Pre-BD FEV1 ResponderFrom first IP dose to Day 84Full analysis setPercentage of ParticipantsNUMBER
SECONDARYChange From Baseline in ACQ-6From first IP dose to Day 84Full analysis setScore on a scaleMEAN
SECONDARYChange From Baseline in St. George's Respiratory Questionnaire (SGRQ)From first IP dose to Day 84Full analysis setScore on a scaleMEAN
SECONDARYChange From Baseline to End of Treatment in FeNOFrom first IP dose to Day 84Full analysis setppbMEAN
SECONDARYChange From Baseline to End of Treatment in Total Lung Capacity (TLC) for Sub-study PatientsFrom first IP dose to Day 84Body plethysmography sub-study analysis setLiterMEAN
SECONDARYChange From Baseline to End of Treatment in Ratio of Residual Volume (RV) and Total Lung Capacity (TLC) for Sub-study PatientsFrom first IP dose to Day 84Body plethysmography sub-study analysis setratioMEAN
SECONDARYChange From Baseline to End of Treatment in Inspiratory Capacity (IC) for Sub-study PatientsFrom first IP dose to Day 84Body plethysmography sub-study analysis setLiterMEAN
SECONDARYChange From Baseline to End of Treatment in Functional Residual Capacity (FRC) for Sub-study PatientsFrom first IP dose to Day 84Body plethysmography sub-study analysis setLiterMEAN
SECONDARYChange From Baseline to End of Treatment in Vital Capacity (VC) for Sub-study PatientsFrom first IP dose to Day 84Body plethysmography sub-study analysis setLiterMEAN
SECONDARYDuration of IP AdministrationFrom first IP to last IPSafety analysis setDaysMEAN
OTHER_PRE_SPECIFIEDSerum Concentration of BenralizumabFrom first dose to end of treatment period (Day 84)PK analysis setng/mLGEOMETRIC_MEAN
OTHER_PRE_SPECIFIEDPK Parameter of Benralizumab (Cmax)First IP dose cycle (ie, data collected on Days 3, 7, 14 and 28)PK analysis setng/mLGEOMETRIC_MEAN
OTHER_PRE_SPECIFIEDAnti-drug Antibody ResponsesFrom first IP dose to end of treatment period (Day 84)Safety analysis setParticipantsCOUNT_OF_PARTICIPANTS
OTHER_PRE_SPECIFIEDChange From Baseline to End of Treatment in PGI-SFrom first IP dose to Day 84Full analysis setScore on a scaleMEAN
OTHER_PRE_SPECIFIEDChange From Baseline to End of Treatment in CGI-CFrom first IP dose to Day 84Full analysis setParticipantsCOUNT_OF_PARTICIPANTS

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.

For software

Read this list from software.

Twenty rows a page, as JSON. No key.

GET https://conductscience.org/api/trials/v1/NCT02869438/outcomes