CV death, myocardial infarction, or stroke
The confidence interval narrowly crossed 1.00, supporting cardiovascular comparability but not a statistically superior reduction in major adverse cardiovascular events.
In adults with type 2 diabetes and established atherosclerotic cardiovascular disease, tirzepatide was cardiovascularly noninferior to dulaglutide, an active comparator with known cardiovascular benefit.
The confidence interval narrowly crossed 1.00, supporting cardiovascular comparability but not a statistically superior reduction in major adverse cardiovascular events.
Safety interpretation should balance cardiovascular comparability with tolerability counseling, especially nausea, vomiting, diarrhea, and other gastrointestinal adverse events.
| Measure | Tirzepatide | Dulaglutide | Effect / interpretation |
|---|---|---|---|
| Patients assigned | 6,586 | 6,579 | 13,165 total in the modified intention-to-treat population |
| Primary CV event CV death, MI, or stroke |
12.2% | 13.1% | HR 0.92; 95.3% CI 0.83–1.01 |
| Cardiovascular conclusion | Noninferior to dulaglutide | Did not meet statistical superiority | |
| Safety | Similar overall adverse-event rates | Gastrointestinal events occurred more frequently with tirzepatide | |
For patients with type 2 diabetes and established cardiovascular disease, tirzepatide demonstrated cardiovascular outcomes comparable to dulaglutide while offering its known metabolic benefits on weight and glycemic control.
Emphasize: noninferior, not proven superior — and balance efficacy messaging with the higher frequency of gastrointestinal adverse events.