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After a 2 week screening period all eligible participants were randomly assigned to treatment groups receiving either a subcutaneous injection of 2.4 mg of semaglutide, 2.4 mg of cagrilintide, a combination of cagrilintide and semaglutide, a semaglutide placebo, or a cagrilintide placebo [2]
Currently, only one study has been conducted on the safety of semaglutide in breastfeeding
Nausea, reflux, constipation, diarrhea, and reduced appetite may occur
Research doses commonly discussed range from 20-100 mcg per site, often administered post-exercise
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