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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]

Possible Side Effects While GACLIV is generally well-tolerated, side effects can occur, especially if improperly administered or overused

Engaging and supporting healthcare professionals, including physicians and nurse practitioners, from all backgrounds to serve as principal investigators and sub-investigators will be critical to fulfilling the need for greater trial diversity

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477 These disability estimates are based on data across U.S