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The published literature on GLP-1 agonists in pediatrics is predominantly from pediatric patients 10-18 years old

PET-CT with F-FDG after controlled cold exposure (16-18C, 2h)

But returning to side effects, we can see the 6mg and 10mg groups have side effect profiles comparable to other drugs weve looked at today and so in my mind those are both viable doses to trial in phase 3

In terms of side effects and tolerability, the advantage goes to neither (comparable)

Recent filings indicate ongoing disputes over the scope of medical record production and expert retention deadlines

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