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
30 June 2027

Inclusion period, 356 days remaining

National Lead

prof. dr. J.H. Cornel

Cardioloog

Study Director

dr. R.M. Oemrawsingh

Cardioloog

Office Contact

M.J. van Doorn

WCN

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