3 results
Primary Objective: The main objective of this prospective clinical trial is to compare pharmacokinetics and safety and tolerability of a standard dose (400 mg) with an escalated dose of 600 and 800 mg MFX. Secondary Objectives: * To evaluate limited…
The study includes 2 periods, Period 1 and Period 2. Subjects will participate in both periods. Period 1:The purpose of Period 1 is to investigate how quickly and to what extent enpatoran is absorbed, transported and eliminated from the body (this…
To assess the effect of prehospital administration of crushed tablets of prasugrel loading dose (in addition to ASA and standard care) on safety and efficacy in patients treated with primary PCI for acute STEMI with last-generation DES (Firehawk*,…