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Trial · NCT03457701

Results by group106

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

OutcomeGroupCategoryValueSpreadUnits
Percentage of Fractional Oral Iron Absorption Following Treatment With Daprodustat and rhEPODaprodustat20.6495% Confidence Interval 10.96 to 30.32Percentage (%) of iron absorbed
Percentage of Fractional Oral Iron Absorption Following Treatment With Daprodustat and rhEPOrhEPO20.6295% Confidence Interval 10.95 to 30.30Percentage (%) of iron absorbed
Periods 1 and 2: Change From Baseline in Serum Iron Following Treatment With Daprodustat and rhEPODaprodustatPeriod 1, DAY 14-1.5Standard Deviation 6.72Micromoles per liter (umol/L)
Periods 1 and 2: Change From Baseline in Serum Iron Following Treatment With Daprodustat and rhEPOrhEPOPeriod 1, DAY 141.7Standard Deviation 4.93Micromoles per liter (umol/L)
Periods 1 and 2: Change From Baseline in Serum Iron Following Treatment With Daprodustat and rhEPODaprodustatPeriod 1, DAY 282.5Standard Deviation 8.96Micromoles per liter (umol/L)
Periods 1 and 2: Change From Baseline in Serum Iron Following Treatment With Daprodustat and rhEPOrhEPOPeriod 1, DAY 283.3Standard Deviation 5.47Micromoles per liter (umol/L)
Periods 1 and 2: Change From Baseline in Serum Iron Following Treatment With Daprodustat and rhEPODaprodustatPeriod 2, DAY 14-1.3Standard Deviation 4.93Micromoles per liter (umol/L)
Periods 1 and 2: Change From Baseline in Serum Iron Following Treatment With Daprodustat and rhEPOrhEPOPeriod 2, DAY 14-3.5Standard Deviation 6.66Micromoles per liter (umol/L)
Periods 1 and 2: Change From Baseline in Serum Iron Following Treatment With Daprodustat and rhEPODaprodustatPeriod 2, DAY 28-2.2Standard Deviation 4.79Micromoles per liter (umol/L)
Periods 1 and 2: Change From Baseline in Serum Iron Following Treatment With Daprodustat and rhEPOrhEPOPeriod 2, DAY 28-3.3Standard Deviation 5.01Micromoles per liter (umol/L)
Period 1 and 2: Change From Baseline in Transferrin Following Treatment With Daprodustat or rhEPODaprodustatPeriod 1, DAY 140.182Standard Deviation 0.2914Gram per Liter (g/L)
Period 1 and 2: Change From Baseline in Transferrin Following Treatment With Daprodustat or rhEPOrhEPOPeriod 1, DAY 140.145Standard Deviation 0.2501Gram per Liter (g/L)
Period 1 and 2: Change From Baseline in Transferrin Following Treatment With Daprodustat or rhEPODaprodustatPeriod 1, DAY 280.283Standard Deviation 0.2824Gram per Liter (g/L)
Period 1 and 2: Change From Baseline in Transferrin Following Treatment With Daprodustat or rhEPOrhEPOPeriod 1, DAY 28-0.040Standard Deviation 0.1756Gram per Liter (g/L)
Period 1 and 2: Change From Baseline in Transferrin Following Treatment With Daprodustat or rhEPODaprodustatPeriod 2, DAY 14-0.177Standard Deviation 0.4664Gram per Liter (g/L)
Period 1 and 2: Change From Baseline in Transferrin Following Treatment With Daprodustat or rhEPOrhEPOPeriod 2, DAY 14-0.163Standard Deviation 0.2461Gram per Liter (g/L)
Period 1 and 2: Change From Baseline in Transferrin Following Treatment With Daprodustat or rhEPODaprodustatPeriod 2, DAY 280.138Standard Deviation 0.2381Gram per Liter (g/L)
Period 1 and 2: Change From Baseline in Transferrin Following Treatment With Daprodustat or rhEPOrhEPOPeriod 2, DAY 28-0.352Standard Deviation 0.2531Gram per Liter (g/L)
Periods 1 and 2: Change From Baseline in Transferrin Saturation Following Treatment With Daprodustat or rhEPODaprodustatPeriod 1, DAY 14-5.2Standard Deviation 13.63Percentage (%) of transferrin saturation
Periods 1 and 2: Change From Baseline in Transferrin Saturation Following Treatment With Daprodustat or rhEPOrhEPOPeriod 1, DAY 143.5Standard Deviation 12.05Percentage (%) of transferrin saturation

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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