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Lixisenatide vs Placebo: Time to First Occurence of CV Event: CV Death, Non-Fatal MI, Non-Fatal Stroke, Hospitalization for Unstable Angina or Hospitalization For Heart Failure

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 10.150.1380.163wilsonClinicalTrials.gov
Risk in group 20.1550.1420.168wilsonClinicalTrials.gov
Risk difference, group 1 minus group 2-0.00428-0.02240.0138newcombe hybrid scoreClinicalTrials.gov
Risk ratio, group 1 over group 20.9720.8631.09logClinicalTrials.gov
Odds ratio, group 1 over group 20.9670.8411.11logClinicalTrials.gov
Number needed to treat, for one fewer participant with the outcome on Lixisenatide than on Placebo233from the risk difference intervalthe interval includes no differenceClinicalTrials.gov

Groups 2

Group 2 names the comparator: placebo.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov codeSource
Group 1LixisenatideLixisenatide 10 mcg QD SC for 2 weeks post-randomization, then at a maintenance dose of 20 mcg QD up to end of treatment (median exposure: 22 months).4563,034OG001ClinicalTrials.gov
Group 2PlaceboPlacebo matched to lixisenatide QD SC up to end of treatment (median exposure: 23 months).4693,034OG000ClinicalTrials.gov

Outcome 5

FieldValueSource
TypeSECONDARYClinicalTrials.gov
TitleTime to First Occurence of CV Event: CV Death, Non-Fatal MI, Non-Fatal Stroke, Hospitalization for Unstable Angina or Hospitalization For Heart FailureClinicalTrials.gov
Description
All CV events were positively adjudicated by the CAC, used in the analysis of the composite CV endpoint comprised of CV death, non-fatal MI, non-fatal stroke, hospitalization for unstable angina or hospitalization for heart failure. Number of observed participants with endpoint events were reported.
ClinicalTrials.gov
Time frameFrom randomization up to the end of study (median follow-up of 25 months)ClinicalTrials.gov
PopulationITT population.ClinicalTrials.gov

Trial 8

FieldValueSource
TitleEvaluation of Cardiovascular Outcomes in Patients With Type 2 Diabetes After Acute Coronary Syndrome During Treatment With AVE0010 (Lixisenatide)ClinicalTrials.gov
NCT numberNCT01147250ClinicalTrials.gov
PhasesPHASE3ClinicalTrials.gov
ConditionsAcute Coronary SyndromeClinicalTrials.gov
InterventionsLixisenatide (AVE0010), PlaceboClinicalTrials.gov
Lead sponsorSanofiClinicalTrials.gov
Results first posted2016-10-14ClinicalTrials.gov
Results on ClinicalTrials.govhttps://clinicaltrials.gov/study/NCT01147250?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.