drugset / Trial / NCT01107886

Does Saxagliptin Reduce the Risk of Cardiovascular Events When Used Alone or Added to Other Diabetes Medications

NCT01107886 ↗

Phase 4 Completed 18206 enrolled AstraZeneca Bristol-Myers Squibb · collab
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The purpose of this study is to determine whether saxagliptin can reduce the risk of cardiovascular events when used alone or added to other diabetes medications

Timeline

Start
2010-05
Primary completion
2013-05
Completion
2013-05

Outcome

Sources disagree · no verdict is set; each source's reading is shown below

paper hazard ratio with saxagliptin, 1.00; 95% confidence interval [CI], 0.89 to 1.12; P=0.99 for superiority; P<0.001 for noninferiority reads as met primary endpoint PMID 23992601 ↗

release “SAVOR met the primary safety objective, demonstrating that ONGLYZA did not increase the risk for cardiovascular death, nonfatal MI and nonfatal ischaemic stroke” reads as mixed primary results astrazeneca.com ↗

release “ONGLYZA did not meet the primary efficacy objective of superiority to placebo for the same composite endpoint.” reads as mixed primary results astrazeneca.com ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject SAXAGLIPTIN ANHYDROUS Small molecule 2.5 mg —
Subject SAXAGLIPTIN ANHYDROUS Small molecule 5 mg —