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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]

Here are the key administration guidelines: Choose injection sites with adequate fatty tissue: Abdomen (avoiding the belly button) Love handles Upper arm area Inner thigh region Always rotate injection sites to prevent tissue damage and maintain absorption efficiency

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This meticulous handling is essential to prevent degradation and ensure the compound retains its full potency throughout the duration of your study