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Dalcetrapib vs Placebo: Composite of Cardiovascular Death, Resuscitated Cardiac Arrest, Non-Fatal Myocardial Infarction, and Non-Fatal Stroke

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 10.09510.08520.106wilsonClinicalTrials.gov
Risk in group 20.1060.09590.118wilsonClinicalTrials.gov
Risk difference, group 1 minus group 2-0.0112-0.02630.00384newcombe hybrid scoreClinicalTrials.gov
Risk ratio, group 1 over group 20.8940.771.04logClinicalTrials.gov
Odds ratio, group 1 over group 20.8830.7481.04logClinicalTrials.gov
Number needed to treat, for one fewer participant with the outcome on Dalcetrapib than on Placebo89.1from the risk difference intervalthe interval includes no differenceClinicalTrials.gov

Groups 2

Group 2 names the comparator: placebo.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov codeSource
Group 1DalcetrapibParticipants received dalcetrapib 600 mg (two 300 mg tablets) orally once daily.~dalcetrapib: Cholesterol Ester Transfer Protein inhibitor, 300 mg tablets2923,071OG001ClinicalTrials.gov
Group 2PlaceboParticipants received dalcetrapib placebo tablets matching dalcetrapib orally once daily.~Placebo: dalcetrapib matching placebo tablets3273,076OG000ClinicalTrials.gov

Outcome 5

FieldValueSource
TypePRIMARYClinicalTrials.gov
TitleComposite of Cardiovascular Death, Resuscitated Cardiac Arrest, Non-Fatal Myocardial Infarction, and Non-Fatal StrokeClinicalTrials.gov
Description
All efficacy endpoints were adjudicated by an independent clinical endpoint committee (CEC). The primary efficacy endpoint was the time from randomization to the first occurrence of any component of the composite endpoint, which included death from cardiovascular causes, resuscitated cardiac arrest, non-fatal myocardial infarction, or non-fatal stroke, as positively adjudicated by the CEC.
ClinicalTrials.gov
Time frameFrom randomization to the first occurrence of any component of the composite primary endpoint (median duration of follow-up was 39.9 months)ClinicalTrials.gov
PopulationAll subjects randomized to treatmentClinicalTrials.gov

Trial 8

FieldValueSource
TitleEffect of Dalcetrapib vs Placebo on CV Risk in a Genetically Defined Population With a Recent ACSClinicalTrials.gov
NCT numberNCT02525939ClinicalTrials.gov
PhasesPHASE3ClinicalTrials.gov
ConditionsAcute Coronary SyndromeClinicalTrials.gov
Interventionsdalcetrapib, PlaceboClinicalTrials.gov
Lead sponsorDalCor PharmaceuticalsClinicalTrials.gov
Results first posted2022-10-12ClinicalTrials.gov
Results on ClinicalTrials.govhttps://clinicaltrials.gov/study/NCT02525939?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.