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[35] reported that in their multicenter, double-blind, event-driven superiority RCT of 17,604 individuals (8803 receiving semaglutide and 8801 receiving placebo) with a mean ( SD) duration of exposure of 34.2 13.7 months, weekly sc semaglutide at a dose of 2.4 mg was superior to placebo in reducing the incidence of death from cardiovascular causes, nonfatal myocardial infarction, or nonfatal stroke at a mean follow-up of 39.8 months

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