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Trial · NCT03001011

Results by group124

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

OutcomeGroupCategoryValueSpreadUnits
Change From Baseline in Serum Phosphorus at Week 8PlaceboBaseline2.090Full Range 1.870 to 2.270mmol/L
Change From Baseline in Serum Phosphorus at Week 8RenvelaBaseline2.095Full Range 1.870 to 2.400mmol/L
Change From Baseline in Serum Phosphorus at Week 8PlaceboChange at Week 80.010Full Range -0.200 to 0.250mmol/L
Change From Baseline in Serum Phosphorus at Week 8RenvelaChange at Week 8-0.200Full Range -0.490 to 0.020mmol/L
Change From Baseline in Total Cholesterol at Week 8Placebo-0.115Full Range -1.82 to 1.54mmol/L
Change From Baseline in Total Cholesterol at Week 8Renvela-0.830Full Range -4.45 to 0.74mmol/L
Change From Baseline in Low-Density Lipoprotein Cholesterol (LDL-C) at Week 8Placebo-0.030Full Range -1.61 to 1.30mmol/L
Change From Baseline in Low-Density Lipoprotein Cholesterol (LDL-C) at Week 8Renvela-0.830Full Range -3.31 to 0.51mmol/L
Change From Baseline in Calcium-Phosphorus Product at Week 8Placebo0.0200Full Range -2.648 to 2.936mmol^2/L^2
Change From Baseline in Calcium-Phosphorus Product at Week 8Renvela-0.4960Full Range -2.592 to 2.696mmol^2/L^2
Change From Baseline in Intact Parathyroid Hormone (Ipth) Level at Week 8Placebo7.2380Full Range -298.732 to 573.306nanogram per liter (ng/L)
Change From Baseline in Intact Parathyroid Hormone (Ipth) Level at Week 8Renvela0.0000Full Range -370.172 to 327.966nanogram per liter (ng/L)
Percentage of Participants Reaching the Target Serum Phosphorus Level (4.6 mg/dL [1.49 mmol/L]) at Week 8Placebo6.6percentage of participants
Percentage of Participants Reaching the Target Serum Phosphorus Level (4.6 mg/dL [1.49 mmol/L]) at Week 8Renvela15.5percentage of participants
Change From Baseline in Serum Phosphorus Level at Week 4Placebo-0.020Full Range -1.56 to 2.42mmol/L
Change From Baseline in Serum Phosphorus Level at Week 4Renvela-0.240Full Range -1.03 to 1.39mmol/L
Number of Participants With Treatment Emergent Adverse EventPlaceboAny TEAE86Participants
Number of Participants With Treatment Emergent Adverse EventRenvelaAny TEAE83Participants
Number of Participants With Treatment Emergent Adverse EventPlaceboAny Treatment emergent SAE31Participants
Number of Participants With Treatment Emergent Adverse EventRenvelaAny Treatment emergent SAE26Participants

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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