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Evacetrapib vs Placebo: Number of Participants With Composite Primary Endpoint of Cardiovascular (CV) Death, Myocardial Infarction (MI), Stroke, Coronary Revascularization, or Hospitalization for Unstable Angina (UA)

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 10.1290.1210.138wilsonClinicalTrials.gov
Risk in group 20.1280.120.137wilsonClinicalTrials.gov
Risk difference, group 1 minus group 20.000837-0.01110.0128newcombe hybrid scoreClinicalTrials.gov
Risk ratio, group 1 over group 21.010.9171.1logClinicalTrials.gov
Odds ratio, group 1 over group 21.010.9061.12logClinicalTrials.gov
Number needed to treat, for one more participant with the outcome on Evacetrapib than on Placebo1,200from the risk difference intervalthe interval includes no differenceClinicalTrials.gov

Groups 2

Group 2 names the comparator: placebo.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov codeSource
Group 1EvacetrapibEvacetrapib 130 mg tablet, administered orally once daily for up to 4 years. Participants received standard of care for HRVD.7796,038OG000ClinicalTrials.gov
Group 2PlaceboPlacebo, tablet administered orally once daily for up to 4 years. Participants received standard of care for HRVD.7766,054OG001ClinicalTrials.gov

Outcome 5

FieldValueSource
TypePRIMARYClinicalTrials.gov
TitleNumber of Participants With Composite Primary Endpoint of Cardiovascular (CV) Death, Myocardial Infarction (MI), Stroke, Coronary Revascularization, or Hospitalization for Unstable Angina (UA)ClinicalTrials.gov
DescriptionFor component endpoints, the number of participants includes those experiencing fatal events and account for all occurrences regardless of whether or not another component event occurred previously.ClinicalTrials.gov
Time frameBaseline to Study Completion (Up to 4 years)ClinicalTrials.gov
PopulationAll randomized participants.ClinicalTrials.gov

Trial 8

FieldValueSource
TitleA Study of Evacetrapib in High-Risk Vascular DiseaseClinicalTrials.gov
NCT numberNCT01687998ClinicalTrials.gov
PhasesPHASE3ClinicalTrials.gov
ConditionsCardiovascular DiseasesClinicalTrials.gov
InterventionsEvacetrapib, PlaceboClinicalTrials.gov
Lead sponsorEli Lilly and CompanyClinicalTrials.gov
Results first posted2018-05-16ClinicalTrials.gov
Results on ClinicalTrials.govhttps://clinicaltrials.gov/study/NCT01687998?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.