highly significantp = 0.006
In this trial, the composite endpoint of cardiovascular death, myocardial infarction, or stroke showed a highly significant reduction favoring prasugrel vs. ticagrelor (HR: 1.36, [95% CI: 1.09–1.70], p = 0.006), and bleeding events did not differ between groups (HR: 1.12, [95% CI: 0.83–1.51], p = 0.45) [ 25 ].