MARITIME-ASCVD PHASE3 ACTIVE
Drug: MariTide · AMGN
Study Design
DesignRandomized, double-blind, placebo-controlled, event-driven outcomes trial
Treatment Arms
MariTide SC (dose TBD)
Placebo Placebo SC
Primary Endpoints
[{"id":"mace","name":"Major adverse cardiovascular events (MACE)","type":"PRIMARY","results":[],"description":"CV outcomes in patients with established ASCVD. SELECT (semaglutide): 20% MACE reduction set the precedent."}]
Assessment
Enrolling. Long-duration outcomes trial. Readout likely 2029+. Source: ClinicalTrials.gov NCT07160257
Background & Context
CV outcomes trial for label claim. SELECT trial established GLP-1 MACE benefit.
Data from Supabase · Updated 2026-03-24