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Saxagliptin vs Placebo: Participants With Any Event From the Composite of CV Death, Non-fatal MI, Non-fatal Ischaemic Stroke, Hospitalisation for Heart Failure, Hospitalisation for Unstable Angina Pectoris, or Hospitalisation for Coronary Revascularisation

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 10.1280.1210.135wilsonClinicalTrials.gov
Risk in group 20.1260.1190.133wilsonClinicalTrials.gov
Risk difference, group 1 minus group 20.00199-0.008180.0121newcombe hybrid scoreClinicalTrials.gov
Risk ratio, group 1 over group 21.020.9381.1logClinicalTrials.gov
Odds ratio, group 1 over group 21.020.9291.12logClinicalTrials.gov
Number needed to treat, for one more participant with the outcome on Saxagliptin than on Placebo504from the risk difference intervalthe interval includes no differenceClinicalTrials.gov

Groups 2

Group 2 names the comparator: placebo.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov codeSource
Group 1Saxagliptin5 mg once daily in subjects with normal renal function or mild impaired renal function (eGFR \>50 mL/min); 2.5 mg once daily in subjects with moderate to severe renal impairment (eGFR ≤50 mL/min).1,0598,280OG000ClinicalTrials.gov
Group 2PlaceboMatching Placebo1,0348,212OG001ClinicalTrials.gov

Outcome 5

FieldValueSource
TypeSECONDARYClinicalTrials.gov
Title
Participants With Any Event From the Composite of CV Death, Non-fatal MI, Non-fatal Ischaemic Stroke, Hospitalisation for Heart Failure, Hospitalisation for Unstable Angina Pectoris, or Hospitalisation for Coronary Revascularisation
ClinicalTrials.gov
Description
Participants with CV death, non-fatal MI, non-fatal ischaemic stroke, hospitalisation for heart failure, hospitalisation for unstable angina pectoris, or hospitalisation for coronary revascularisation. If no event, censoring occurs at the patient withdrawal of consent, last contact, or death (when applicable)-whichever was later.
ClinicalTrials.gov
Time frameRandomization (day 0) up to 2.9 yearsClinicalTrials.gov
PopulationIntention To Treat (ITT) analysis of randomized population. Events were adjudicated by the Clinical Event Adjudication Committee.ClinicalTrials.gov

Trial 8

FieldValueSource
TitleDoes Saxagliptin Reduce the Risk of Cardiovascular Events When Used Alone or Added to Other Diabetes MedicationsClinicalTrials.gov
NCT numberNCT01107886ClinicalTrials.gov
PhasesPHASE4ClinicalTrials.gov
ConditionsType 2 Diabetes MellitusClinicalTrials.gov
InterventionsSaxagliptin, PlaceboClinicalTrials.gov
Lead sponsorAstraZenecaClinicalTrials.gov
Results first posted2014-06-13ClinicalTrials.gov
Results on ClinicalTrials.govhttps://clinicaltrials.gov/study/NCT01107886?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.