Human study regimen: Amount: 0.1 mg/kg/min IV; 5 µg/mL in cardioplegia; Route: Intravenous infusion plus cardioplegia; Frequency: Perioperative; Duration: Approximately 7 hours for the IV infusion; Species: Human; Population: Adults undergoing coronary artery bypass grafting
Limitations: The randomized trial did not demonstrate a significant benefit on its primary composite endpoint.