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

Stadium
inclusie
Middel
Selatogrel
Populatie
ASCVD
Fase
III
First Patient In
9 mei 2022
Last Patient In
1 juni 2026
Last Patient Last Visit
1 september 2026

Inclusieperiode, nog 184 dagen over

National Lead

prof. dr. J.H. Cornel

Cardioloog

Studiedirecteur

dr. R.M. Oemrawsingh

Cardioloog

Contact Kantoor

S. Jansen

Studiemanager

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