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FDA approval is expected in late 2027 or early 2028, with commercial launch following 13 months later

Its extended amino acid sequence, along with specific substitutions such as -aminoisobutyric acid (Aib) residues, enhances structural stability and receptor interaction in controlled research environments

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Whilst gastrointestinal side effects such as nausea, diarrhoea, and constipation are common with Ozempic, blood in stool is not a recognised adverse reaction in UK regulatory data

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