drugset / Trial / NCT01131676

BI 10773 (Empagliflozin) Cardiovascular Outcome Event Trial in Type 2 Diabetes Mellitus Patients (EMPA-REG OUTCOME).

NCT01131676 ↗

Phase 3 Completed 7064 enrolled Boehringer Ingelheim Eli Lilly and Company · collab
RandomizedParallel-groupDouble-blindTreatment

Summary

The aim of the present study is to investigate the safety of BI 10773 treatment in patients with Type 2 Diabetes Mellitus and high cardiovascular risk.

Timeline

Start
2010-07
Primary completion
2015-04
Completion
2015-04

Outcome

Met primary endpoint

registry Placebo vs All Empagliflozin; p = 0.0382; Hazard Ratio (HR) 0.86 (95.02% CI 0.74 to 0.99) NCT01131676 ↗

paper The primary outcome occurred in 490 of 4687 patients (10.5%) in the pooled empagliflozin group and in 282 of 2333 patients (12.1%) in the placebo group PMID 26378978 ↗

release “EMPA-REG OUTCOME met its primary endpoint and demonstrated superiority of JARDIANCE, when added to standard of care, in CV risk reduction.” lilly.com ↗

release “EMPA-REG OUTCOME® trial, which found that JARDIANCE significantly reduced the risk of the combined endpoint” lilly.com ↗

release “Over a median of 3.1 years, JARDIANCE significantly reduced the risk of CV death, non-fatal heart attack or non-fatal stroke by 14 percent versus placebo.” lilly.com ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Empagliflozin Small molecule 10 mg Oral
Subject Empagliflozin Small molecule 25 mg Oral