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Finerenone vs Placebo: deaths from any cause

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 10.0920.08310.102wilsonClinicalTrials.gov
Risk in group 20.1040.0950.115wilsonClinicalTrials.gov
Risk difference, group 1 minus group 2-0.0125-0.02610.00111newcombe hybrid scoreClinicalTrials.gov
Risk ratio, group 1 over group 20.880.7661.01logClinicalTrials.gov
Odds ratio, group 1 over group 20.8680.7441.01logClinicalTrials.gov
Number needed to treat, for one fewer death from any cause on Finerenone than on Placebo80from the risk difference intervalthe interval includes no differenceClinicalTrials.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 therapy3393,686EG000ClinicalTrials.gov
Group 2PlaceboParticipants received matching placebo once daily in addition to standard of care therapy3833,666EG001ClinicalTrials.gov

Harm 2

FieldValueSource
What it countsTotal, all-cause mortalityClinicalTrials.gov
Time frameAfter the first dose of study drug up to 3 days after any temporary or permanent interruption of study drug, with an average treatment duration of 36 months.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.