ConductScience.org, home

Library / Trial comparisons

Finerenone vs Placebo: The First Occurrence of the Composite Endpoint of Cardiovascular Death, Non-fatal Myocardial Infarction, Non Fatal Stroke, or Hospitalization for Heart Failure.

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

Measures 6

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

MeasureValue95% interval, lower95% interval, upperMethodNoteSource
Risk in group 10.1240.1140.135wilsonClinicalTrials.gov
Risk in group 20.1420.1310.153wilsonClinicalTrials.gov
Risk difference, group 1 minus group 2-0.0173-0.0328-0.00179newcombe hybrid scoreClinicalTrials.gov
Risk ratio, group 1 over group 20.8780.7810.987logClinicalTrials.gov
Odds ratio, group 1 over group 20.860.7520.985logClinicalTrials.gov
Number needed to treat, for one fewer participant with the outcome on Finerenone than on Placebo57.730.4557from the risk difference intervalClinicalTrials.gov

Groups 2

Group 2 names the comparator: placebo.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov codeSource
Group 1FinerenoneParticipants received finerenone 10 mg or 20 mg once daily in addition to standard of care therapy4583,686OG000ClinicalTrials.gov
Group 2PlaceboParticipants received matching placebo once daily in addition to standard of care therapy5193,666OG001ClinicalTrials.gov

Outcome 5

FieldValueSource
TypePRIMARYClinicalTrials.gov
TitleThe First Occurrence of the Composite Endpoint of Cardiovascular Death, Non-fatal Myocardial Infarction, Non Fatal Stroke, or Hospitalization for Heart Failure.ClinicalTrials.gov
Description
Number of participants with the first occurrence of the primary cardiovascular (CV) composite outcome, CV death, non-fatal myocardial infarction (MI), non-fatal stroke, or hospitalization for heart failure were reported as descriptive result.
ClinicalTrials.gov
Time frameFrom randomization up until the first occurrence of the CV composite endpoint, or censoring at the end of the study, with an average study duration of 41 months.ClinicalTrials.gov
PopulationFull analysis set (FAS)ClinicalTrials.gov

Trial 8

FieldValueSource
TitleEfficacy and Safety of Finerenone in Subjects With Type 2 Diabetes Mellitus and the Clinical Diagnosis of Diabetic Kidney DiseaseClinicalTrials.gov
NCT numberNCT02545049ClinicalTrials.gov
PhasesPHASE3ClinicalTrials.gov
ConditionsDiabetic Kidney DiseaseClinicalTrials.gov
InterventionsFinerenone (BAY94-8862), PlaceboClinicalTrials.gov
Lead sponsorBayerClinicalTrials.gov
Results first posted2022-04-15ClinicalTrials.gov
Results on ClinicalTrials.govhttps://clinicaltrials.gov/study/NCT02545049?tab=resultsClinicalTrials.gov

Source 4

FieldValueSource
Releasetrial-comparisons-2026-03-23-0.1.0ClinicalTrials.gov
Release manifest SHA-256f66225897fbf258b57ea10bdacfd0347d3cdfda93f7f5685234b7e06ea36fa57ClinicalTrials.gov
AACT copy2026-03-23ClinicalTrials.gov
Tables readoutcome_counts.parquet, outcome_measurements.parquet, outcomes.parquet, reported_event_totals.parquet, reported_events.parquet, result_groups.parquet, studies.parquet, ctgov_trial.parquetClinicalTrials.gov

The same record as JSON

Release trial-comparisons-2026-03-23-0.1.0

ClinicalTrials.gov's posted results, through CTTI's AACT: ClinicalTrials.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.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.

ClinicalTrials.gov: none 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.