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Trial · NCT03299244

Results by group35

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

OutcomeGroupCategoryValueSpreadUnits
Percentage of Participants With > 30% Reduction From Baseline in Mean Predialysis Intact Parathyroid Hormone During the Efficacy Assessment Phase - Non-inferiority AnalysisCinacalcet66.2percentage of participants
Percentage of Participants With > 30% Reduction From Baseline in Mean Predialysis Intact Parathyroid Hormone During the Efficacy Assessment Phase - Non-inferiority AnalysisEtelcalcetide71.9percentage of participants
Percentage of Participants With > 50% Reduction From Baseline in Mean Predialysis iPTH During the Efficacy Assessment PhaseCinacalcet41.6percentage of participants
Percentage of Participants With > 50% Reduction From Baseline in Mean Predialysis iPTH During the Efficacy Assessment PhaseEtelcalcetide59.1percentage of participants
Percentage of Participants With > 30% Reduction From Baseline in Mean Predialysis iPTH During the Efficacy Assessment Phase - Superiority AnalysisCinacalcet58.0percentage of participants
Percentage of Participants With > 30% Reduction From Baseline in Mean Predialysis iPTH During the Efficacy Assessment Phase - Superiority AnalysisEtelcalcetide66.3percentage of participants
Percent Change From Baseline in Mean Predialysis Corrected Calcium During the Efficacy Assessment PhaseCinacalcet-8.00Standard Error 0.50percent change
Percent Change From Baseline in Mean Predialysis Corrected Calcium During the Efficacy Assessment PhaseEtelcalcetide-10.69Standard Error 0.53percent change
Percentage of Participants With Mean Predialysis Serum Phosphorus ≤ 4.5 mg/dL During the Efficacy Assessment PhaseCinacalcet26.2percentage of participants
Percentage of Participants With Mean Predialysis Serum Phosphorus ≤ 4.5 mg/dL During the Efficacy Assessment PhaseEtelcalcetide29.1percentage of participants
Number of Participants With cCa < 8.3 mg/dL At Any Time During the StudyCinacalcet245Participants
Number of Participants With cCa < 8.3 mg/dL At Any Time During the StudyEtelcalcetide273Participants
Number of Participants With cCa < 8.0 mg/dL At Any Time During the StudyCinacalcet194Participants
Number of Participants With cCa < 8.0 mg/dL At Any Time During the StudyEtelcalcetide241Participants
Number of Participants With cCa < 7.5 mg/dL At Any Time During the StudyCinacalcet61Participants
Number of Participants With cCa < 7.5 mg/dL At Any Time During the StudyEtelcalcetide109Participants
Number of Participants With Treatment-emergent Symptomatic Hypocalcemia During the StudyCinacalcet15Participants
Number of Participants With Treatment-emergent Symptomatic Hypocalcemia During the StudyEtelcalcetide35Participants
Number of Participants Who Developed Antibodies to EtelcalcetideEtelcalcetide18Participants
Number of Participants With Treatment-emergent Adverse EventsCinacalcetAny treatment-emergent adverse event (TEAE)303Participants

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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