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Comparison · NCT03299244-ce0095c1

Cinacalcet vs Etelcalcetide: Number of Participants With cCa < 8.0 mg/dL At Any Time During the Study

Calculated by ConductScience from the counts the trial posted to ClinicalTrials.gov.

2 sourcestrial-comparisons-2026-03-23-0.1.0

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ConductScience Library. Cinacalcet vs Etelcalcetide: Number of Participants With cCa < 8.0 mg/dL At Any Time During the Study. Trial comparisons, record NCT03299244-ce0095c1. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT03299244-ce0095c1

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Measures6

Calculated by ConductScience from the counts the trial posted to ClinicalTrials.gov.

MeasureValue95% interval, lower95% interval, upperMethodNote
Risk in group 10.6260.5710.678wilson
Risk in group 20.760.710.804wilson
Risk difference, group 1 minus group 2-0.134-0.205-0.0623newcombe hybrid score
Risk ratio, group 1 over group 20.8230.740.915log
Odds ratio, group 1 over group 20.5270.3730.745log
Number needed to treat, for one fewer participant with the outcome on Cinacalcet than on Etelcalcetide7.444.8816from the risk difference interval

Groups2

Neither group, or both, names a comparator, so the groups keep ClinicalTrials.gov's order.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1Cinacalcet
Participants were randomized to receive oral cinacalcet once daily and placebo intravenous (IV) bolus injection at the end of each hemodialysis session three times per week (TIW) for 26 weeks. The starting dose of cinacalcet was 25 mg daily and could have been titrated at weeks 5, 9, 13, and 17 to target predialysis serum PTH ≤ 300 pg/mL but no lower than 100 pg/mL while maintaining cCa ≥ 8.3 mg/dL.
194310OG000
Group 2Etelcalcetide
Participants were randomized to receive etelcalcetide administered by IV bolus injection at the end of each hemodialysis session TIW and daily oral doses of placebo tablets for 26 weeks. The starting dose of etelcalcetide was 5 mg, and could have been titrated at weeks 5, 9, 13, and 17 to target predialysis serum PTH ≤ 300 pg/mL but no lower than 100 pg/mL while maintaining cCa ≥ 8.3 mg/dL.
241317OG001

Outcome

Type
OTHER_PRE_SPECIFIED
Title
Number of Participants With cCa < 8.0 mg/dL At Any Time During the Study
Description
Corrected calcium was measured by the central laboratory.
Time frame
From first dose of study drug to end of study; up to 26 weeks + 30 days.
Population
Participants in the safety analysis set with at least 1 post-baseline cCa value.

Source ClinicalTrials.gov

Trial

Title
Head-to-Head Study of Etelcalcetide and Cinacalcet in Asian Hemodialysis Patients With Secondary Hyperparathyroidism (SHPT)
NCT number
NCT03299244
Phases
PHASE3
Conditions
Secondary Hyperparathyroidism, Chronic Kidney Disease
Interventions
Etelcalcetide, Cinacalcet
Lead sponsor
Amgen
Results first posted
2021-04-30

Source ClinicalTrials.gov

Source

Release
trial-comparisons-2026-03-23-0.1.0
Release manifest SHA-256
f66225897fbf258b57ea10bdacfd0347d3cdfda93f7f5685234b7e06ea36fa57
AACT copy
2026-03-23
Tables read
outcome_counts.parquet, outcome_measurements.parquet, outcomes.parquet, reported_event_totals.parquet, reported_events.parquet, result_groups.parquet, studies.parquet, ctgov_trial.parquet

Source ClinicalTrials.gov

Sources 2

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNo license stated
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

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions. The measures are ConductScience's calculation from them.

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