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Darapladib vs Placebo: Number of Participants With First Occurrence of MI (Fatal/Non-fatal) During the Time Period for Follow-up of CV Events

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 10.04560.04120.0504wilsonClinicalTrials.gov
Risk in group 20.05120.04660.0563wilsonClinicalTrials.gov
Risk difference, group 1 minus group 2-0.00568-0.01240.00101newcombe hybrid scoreClinicalTrials.gov
Risk ratio, group 1 over group 20.8890.7741.02logClinicalTrials.gov
Odds ratio, group 1 over group 20.8840.7641.02logClinicalTrials.gov
Number needed to treat, for one fewer participant with the outcome on Darapladib than on Placebo176from the risk difference intervalthe interval includes no differenceClinicalTrials.gov

Groups 2

Group 2 names the comparator: placebo.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov codeSource
Group 1DarapladibParticipants were randomized to receive darapladib 160 milligram (mg) enteric-coated tablets once daily.3617,924OG001ClinicalTrials.gov
Group 2PlaceboParticipants were randomized to receive matching placebo once daily.4057,904OG000ClinicalTrials.gov

Outcome 5

FieldValueSource
TypeSECONDARYClinicalTrials.gov
TitleNumber of Participants With First Occurrence of MI (Fatal/Non-fatal) During the Time Period for Follow-up of CV EventsClinicalTrials.gov
Description
Acute MI is defined as evidence of myocardial necrosis in a clinical setting consistent with myocardial ischemia. Prior MI diagnosed post-randomization (e.g., silent MI)=the development of new pathological Q waves with/without symptoms OR imaging evidence of a region of loss of viable myocardium that is thinned and fails to contract, in the absence of a non-ischemic cause (pre-event imaging data required for verification of new abnormality), OR pathological findings of a healed/healing MI.
ClinicalTrials.gov
Time frameFrom randomization until the End-of-Treatment visit or the last date on which endpoints were able to be assessed (up to 4.25 years/average of 3.51 years)ClinicalTrials.gov
PopulationAll Randomized (ITT) PopulationClinicalTrials.gov

Trial 8

FieldValueSource
TitleThe Stabilization of Atherosclerotic Plaque by Initiation of Darapladib Therapy TrialClinicalTrials.gov
NCT numberNCT00799903ClinicalTrials.gov
PhasesPHASE3ClinicalTrials.gov
ConditionsAtherosclerosisClinicalTrials.gov
InterventionsDarapladib, PlaceboClinicalTrials.gov
Lead sponsorGlaxoSmithKlineClinicalTrials.gov
Results first posted2017-08-10ClinicalTrials.gov
Results on ClinicalTrials.govhttps://clinicaltrials.gov/study/NCT00799903?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.