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It is also the maximum approved dose for pediatric patients in the eligible age group

Randomization and masking Randomization (1:1) to semaglutide 2.4 mg or placebo was done centrally by the clinical research organization (Parexel) in a double-blind manner using an interactive web-based response system (IWRS) with a fixed-size blocking schema, without stratification

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Side effects are most common at the start of treatment or after increasing the dose , as the body adapts to the medication

This is an important finding because it suggests that the GLP-1 system does play a direct role in anxiety regulation, not just an indirect one