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Darapladib 160 mg vs Placebo: Number of Participants With All-cause Mortality During the Time Period for Vital Status

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 10.05780.05240.0637wilsonClinicalTrials.gov
Risk in group 20.06180.05620.0679wilsonClinicalTrials.gov
Risk difference, group 1 minus group 2-0.00398-0.01210.00417newcombe hybrid scoreClinicalTrials.gov
Risk ratio, group 1 over group 20.9360.8161.07logClinicalTrials.gov
Odds ratio, group 1 over group 20.9320.8061.08logClinicalTrials.gov
Number needed to treat, for one fewer participant with the outcome on Darapladib 160 mg than on Placebo251from the risk difference intervalthe interval includes no differenceClinicalTrials.gov

Groups 2

Group 2 names the comparator: placebo.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov codeSource
Group 1Darapladib 160 mgParticipants were randomized to receive darapladib 160 mg enteric-coated tablets once daily.3766,504OG001ClinicalTrials.gov
Group 2PlaceboParticipants were randomized to receive matching placebo once daily.4036,522OG000ClinicalTrials.gov

Outcome 5

FieldValueSource
TypeSECONDARYClinicalTrials.gov
TitleNumber of Participants With All-cause Mortality During the Time Period for Vital StatusClinicalTrials.gov
Description
Number of participants who died, during the vital status time-period were reported. The participants who were known to have died, date of death was used; for participants who completed the study the study completion date was used; for participants who withdrew from the study where vital status was ascertained , and are known to have not died , the last known date to be alive was used and for participants whom vital status was not ascertained, following study withdrawal the study withdrawal date was used.
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 3.80 years)ClinicalTrials.gov
PopulationAll-Randomized ITT PopulationClinicalTrials.gov

Trial 8

FieldValueSource
TitleThe Stabilization Of pLaques usIng Darapladib-Thrombolysis In Myocardial Infarction 52 TrialClinicalTrials.gov
NCT numberNCT01000727ClinicalTrials.gov
PhasesPHASE3ClinicalTrials.gov
ConditionsAcute Coronary SyndromeClinicalTrials.gov
InterventionsDarapladib 160 mg, Placebo, Standard TherapyClinicalTrials.gov
Lead sponsorGlaxoSmithKlineClinicalTrials.gov
Results first posted2017-08-10ClinicalTrials.gov
Results on ClinicalTrials.govhttps://clinicaltrials.gov/study/NCT01000727?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.