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[18] The NHS and NICE have incorporated this evidence into clinical guidance (NG28), recognising GLP-1 receptor agonists as valuable therapeutic options for patients with type 2 diabetes
This modification gives semaglutide a half-life of approximately seven days, making once-weekly dosing possible
Once submitted, the FDA has about 60 days to accept the application and assign a PDUFA date, after which the 612 month review period begins (6 months if priority review is granted, 1012 months under standard review)
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