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The median follow up was 5.4 year, 12.0% of the patients receiving dulaglutide and 13.4% of those assigned to the placebo group experienced the primary composite endpoint of non-fatal myocardial infarction, non-fatal stroke, or death from cardiovascular causes ( p = 0.026)

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An orally active allosteric Glp-1 receptor agonist is neuroprotective in cellular and rodent models of stroke