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Trial · NCT03409107

Results by group96

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

OutcomeGroupCategoryValueSpreadUnits
Mean Change in Hemoglobin From Baseline and Over the Evaluation Period (Mean Over Week 24 and 28)Placebo0.19Standard Error 0.062Grams per deciliter
Mean Change in Hemoglobin From Baseline and Over the Evaluation Period (Mean Over Week 24 and 28)Daprodustat1.58Standard Error 0.061Grams per deciliter
Percentage of Participants With Hemoglobin Increase of >=1.0 Grams Per Deciliter From Baseline to Evaluation PeriodPlacebo18Percentage of participants
Percentage of Participants With Hemoglobin Increase of >=1.0 Grams Per Deciliter From Baseline to Evaluation PeriodDaprodustat77Percentage of participants
Change From Baseline in Short Form-36 (SF-36) Questionnaire Vitality Domain Score by Traditional Scoring at Week 28Placebo1.93Standard Error 1.161Scores on a scale
Change From Baseline in Short Form-36 (SF-36) Questionnaire Vitality Domain Score by Traditional Scoring at Week 28Daprodustat7.29Standard Error 1.121Scores on a scale
Percentage of Participants With Hgb Response (Hgb in the 11-12 Grams/Deciliter Range) During Evaluation Period (Week 24 to Week 28 Inclusive)Placebo8Percentage of participants
Percentage of Participants With Hgb Response (Hgb in the 11-12 Grams/Deciliter Range) During Evaluation Period (Week 24 to Week 28 Inclusive)Daprodustat52Percentage of participants
Percentage of Time With Hgb Within the Target Range (11-12 Grams Per Deciliter) During Evaluation Period (Week 24 to Week 28 Inclusive) (Hodges-Lehmann Estimate)Placebo0.00Full Range 0.0 to 100.0Percentage of days
Percentage of Time With Hgb Within the Target Range (11-12 Grams Per Deciliter) During Evaluation Period (Week 24 to Week 28 Inclusive) (Hodges-Lehmann Estimate)Daprodustat53.59Full Range 0.0 to 100.0Percentage of days
Percentage of Time With Hgb Within the Target Range (11-12 Grams Per Deciliter) During Evaluation Period (Week 24 to Week 28 Inclusive) (Mann-Whitney Estimate)Placebo0.00Full Range 0.0 to 100.0Percentage of days
Percentage of Time With Hgb Within the Target Range (11-12 Grams Per Deciliter) During Evaluation Period (Week 24 to Week 28 Inclusive) (Mann-Whitney Estimate)Daprodustat53.59Full Range 0.0 to 100.0Percentage of days
Change From Baseline in Post-randomization Hgb at Week 28Placebo0.20Standard Error 0.070Grams per deciliter
Change From Baseline in Post-randomization Hgb at Week 28Daprodustat1.56Standard Error 0.069Grams per deciliter
Rate of Participants Permanently Stopping Randomized Treatment Due to Meeting Rescue CriteriaPlacebo18.8895% Confidence Interval 12.33 to 27.66Events per 100 person year
Rate of Participants Permanently Stopping Randomized Treatment Due to Meeting Rescue CriteriaDaprodustat1.3395% Confidence Interval 0.16 to 4.82Events per 100 person year
Change From Baseline by Domain and Single Item Scores on the Chronic Kidney Disease -Anemia Questionnaire (CKD-AQ) Symptom QuestionnairePlaceboTired/Low Energy/Weak Domain2.81Standard Error 1.132Scores on a scale
Change From Baseline by Domain and Single Item Scores on the Chronic Kidney Disease -Anemia Questionnaire (CKD-AQ) Symptom QuestionnaireDaprodustatTired/Low Energy/Weak Domain8.72Standard Error 1.086Scores on a scale
Change From Baseline by Domain and Single Item Scores on the Chronic Kidney Disease -Anemia Questionnaire (CKD-AQ) Symptom QuestionnairePlaceboChest Pain/Shortness of Breath Domain0.62Standard Error 0.971Scores on a scale
Change From Baseline by Domain and Single Item Scores on the Chronic Kidney Disease -Anemia Questionnaire (CKD-AQ) Symptom QuestionnaireDaprodustatChest Pain/Shortness of Breath Domain3.55Standard Error 0.932Scores on a scale

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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