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Visible improvements in brightness and texture can be seen within 46 weeks
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]
The neurodegenerative potential varies between different forms of A peptides, for example, amyloid aggregates primarily comprise A42, which has higher amyloidogenicity and lower solubility than A40 [48, 49]
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