drugset / Trial / NCT05754957

A Study of Milvexian in Participants After a Recent Acute Coronary Syndrome

NCT05754957

RandomizedParallel-groupQuadruple-blindTreatment

Summary

The purpose of this study is to evaluate that milvexian is superior to placebo, in addition to standard-of-care, in reducing the risk of major adverse cardiovascular event (MACE) (the composite of cardiovascular \[CV\] death, myocardial infarction \[MI\], and ischemic stroke).

Timeline

Start
2023-04-07
Primary completion
2026-02-06
Completion
2026-02-06

Drugs

EvaluationDrugModalityDoseRoute
Subject Milvexian Small molecule 25 mg Oral