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S2A and Fig
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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]
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Because it stimulates the pituitary gland to release the bodys own natural growth hormone, treatment generally requires time before patients notice meaningful changes
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