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Although we may not have sufficient power to detect significant changes in our secondary outcomes (tau PET, MRIs, CSF AD biomarkers and cognition), including a nine-month follow-up will help provide preliminary evidence of successful modification of disease trajectory over a one-year period

169175, doi:10.1053/j.jrn.2014.10.025, PMID 25600394

Food and Drug Administration (FDA) approved 2.4-mg doses of semaglutide as a way reduce the risk of major adverse cardiovascular events in patients who are overweight or obese and present with cardiovascular disease (CVD)