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Trial · NCT03548220

Results by group47

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

OutcomeGroupCategoryValueSpreadUnits
Percentage of Participants Achieving a Hemoglobin (Hb) Response (HR)Placebo Comparator: Placebo0percentage of participants
Percentage of Participants Achieving a Hemoglobin (Hb) Response (HR)Experimental: AG-34840.0percentage of participants
Average Change From Baseline in Hb Concentration at Weeks 16, 20 and 24Placebo Comparator: Placebo-1.48Standard Error 2.082grams per liter (g/L)
Average Change From Baseline in Hb Concentration at Weeks 16, 20 and 24Experimental: AG-34816.73Standard Error 2.075grams per liter (g/L)
Maximum Change From Baseline in Hb ConcentrationPlacebo Comparator: Placebo4.76Standard Deviation 4.217g/L
Maximum Change From Baseline in Hb ConcentrationExperimental: AG-34823.94Standard Deviation 21.367g/L
Time to Achieve an Increase in Hb Concentration of 1.5 g/dL or MoreExperimental: AG-3487.66Standard Deviation 4.050weeks
Average Change From Baseline in Indirect Bilirubin at Weeks 16, 20 and 24Placebo Comparator: Placebo5.10Standard Error 4.061micromoles per liter (μmol/L)
Average Change From Baseline in Indirect Bilirubin at Weeks 16, 20 and 24Experimental: AG-348-21.16Standard Error 4.228micromoles per liter (μmol/L)
Average Change From Baseline in Lactic Acid Dehydrogenase (LDH) at Weeks 16, 20 and 24Placebo Comparator: Placebo-21.18Standard Error 16.040units per litre (U/L)
Average Change From Baseline in Lactic Acid Dehydrogenase (LDH) at Weeks 16, 20 and 24Experimental: AG-348-91.99Standard Error 16.222units per litre (U/L)
Average Change From Baseline in Haptoglobin at Weeks 16, 20 and 24Placebo Comparator: Placebo0.012Standard Error 0.0412g/L
Average Change From Baseline in Haptoglobin at Weeks 16, 20 and 24Experimental: AG-3480.169Standard Error 0.0408g/L
Average Change From Baseline in Reticulocyte Percentages at Weeks 16, 20 and 24Placebo Comparator: Placebo0.0038Standard Error 0.01390Reticulocyte percentages
Average Change From Baseline in Reticulocyte Percentages at Weeks 16, 20 and 24Experimental: AG-348-0.0973Standard Error 0.01401Reticulocyte percentages
Change From Baseline in Pyruvate Kinase Deficiency Diary (PKDD) Score at Week 24Placebo Comparator: Placebo-2.05Standard Error 0.976score on a scale
Change From Baseline in Pyruvate Kinase Deficiency Diary (PKDD) Score at Week 24Experimental: AG-348-5.16Standard Error 0.955score on a scale
Change From Baseline in Pyruvate Kinase Deficiency Impact Assessment (PKDIA) Score at Week 24Placebo Comparator: Placebo-1.39Standard Error 1.157score on a scale
Change From Baseline in Pyruvate Kinase Deficiency Impact Assessment (PKDIA) Score at Week 24Experimental: AG-348-4.65Standard Error 1.123score on a scale
Percentage of Participants With Adverse EventsPlacebo Comparator: Placebo89.7percentage 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.

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