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The SELECT cardiovascular outcomes trial (N=17,604) demonstrated that semaglutide 2.4 mg reduced major adverse cardiovascular events (MACE) by 20% over a mean follow-up of 39.8 months, a finding that strengthens re-authorization arguments for patients with established cardiovascular disease [5]
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Increase by one teaspoon every 3-4 days as tolerated
Results from the EVOKE trials, the largest clinical study to date with the GLP-1 drug semaglutide in Alzheimers disease, showed that semaglutide did not significantly slow disease progression in people with early-stage Alzheimers
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