SOS-AMI

Multi-center, double-blind, randomized, placebo-controlled, parallel-group study to evaluate the efficacy and safety of self-administered subcutaneous selatogrel for prevention of all-cause death and treatment of acute myocardial infarction in subjects with a recent history of acute myocardial infarction

Stage
inclusie
Medicine
Selatogrel
Population
ASCVD
Phase
III
First Patient In
9 May 2022
Last Patient In
31 December 2026
Last Patient Last Visit
-

Inclusion period, 377 days remaining

National Lead

prof. dr. J.H. Cornel

Cardioloog

Study Director

dr. R.M. Oemrawsingh

Cardioloog

Office Contact

S. Jansen

Studiemanager

The page has expired.