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Trial · NCT01147666

Participant flow150

How many started, completed or left each group, period by period.

PeriodMilestoneGroupParticipantsUnits counted
Dosing Period 1: 6-Week TreatmentEfficacy Evaluable (EE) PopulationCohorts A (Epoetin Alfa)31
Dosing Period 1: 6-Week TreatmentEfficacy Evaluable (EE) PopulationCohort B-1 (Roxadustat 1.5 mg/kg TIW)1
Dosing Period 1: 6-Week TreatmentEfficacy Evaluable (EE) PopulationCohort B-2 (Roxadustat 2.0 mg/kg TIW)3
Dosing Period 1: 6-Week TreatmentEfficacy Evaluable (EE) PopulationCohort B (Epoetin Alfa)4
Dosing Period 1: 6-Week TreatmentEfficacy Evaluable (EE) PopulationCohort B (Placebo)3
Dosing Period 1: 6-Week TreatmentCOMPLETEDCohort A-1 (Roxadustat 1.0 mg/kg TIW)10
Dosing Period 1: 6-Week TreatmentCOMPLETEDCohort A-2 (Roxadustat 1.5 mg/kg TIW)10
Dosing Period 1: 6-Week TreatmentCOMPLETEDCohort A-3 (Roxadustat 2.0 mg/kg TIW)11
Dosing Period 1: 6-Week TreatmentCOMPLETEDCohort A-4 (Roxadustat 1.8 mg/kg TIW)10
Dosing Period 1: 6-Week TreatmentCOMPLETEDCohort A-5 (Roxadustat 1.8 mg/kg TIW)7
Dosing Period 1: 6-Week TreatmentCOMPLETEDCohort A-6 (Roxadustat 1.3 mg/kg TIW)9
Dosing Period 1: 6-Week TreatmentCOMPLETEDCohort A-7 (Weight Tiered Roxadustat 70-100-150 mg)9
Dosing Period 1: 6-Week TreatmentCOMPLETEDCohort A-8 (Weight Tiered Roxadustat 70-120-200 mg)9
Dosing Period 1: 6-Week TreatmentCOMPLETEDCohort A-9 (Roxadustat 2.0 mg/kg)2
Dosing Period 1: 6-Week TreatmentCOMPLETEDCohort A-10 (Weight Tiered Roxadustat 70-120-200 mg)8
Dosing Period 1: 6-Week TreatmentCOMPLETEDCohorts A (Epoetin Alfa)33
Dosing Period 1: 6-Week TreatmentCOMPLETEDCohort B-1 (Roxadustat 1.5 mg/kg TIW)2
Dosing Period 1: 6-Week TreatmentCOMPLETEDCohort B-2 (Roxadustat 2.0 mg/kg TIW)1
Dosing Period 1: 6-Week TreatmentCOMPLETEDCohort B (Epoetin Alfa)3
Dosing Period 1: 6-Week TreatmentCOMPLETEDCohort B (Placebo)0

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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