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The SURPASS-CVOT trial, where dulaglutide at the dose of 1.5 mg/week or at the highest tolerated dose, is the comparator, has a distinctive design from the other trials: the primary endpoint is the time to the first manifestation of any major adverse CV event (MACE), defined as myocardial infarction, stroke or CV death

Enzyme activity was shown as fold changes in absorbance per minute normalized to substrates only group

"Seventy percent of consumers in the survey say they're working on diet as part of their weight loss journey

If they are looking in the mirror and seeing a heavy person when they are not a heavy person, consider mental health help for them. Referrals are welcome The Nebraska Medicine Bariatric Center is the region's most comprehensive weight-management program

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