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Semaglutide is a 31 amino acid analog of native glucagon like peptide 1 with a fatty acid side chain that binds albumin and extends half life to roughly seven days
We are licenced to administer this treatment following a face-to-face consultation which establishes this is necessary and suitable
B12therapy is not intended to diagnose, treat, or prevent any disease
Under standard review timelines of 6-10 months, regulatory approval could come shortly after
FDA's evaluation concluded that the criteria weighed against placement on the list, citing inadequate physicochemical characterization, immunogenicity concerns from impurities and aggregates, lack of clinical effectiveness data for any approved use, and absence of published human exposure data for the proposed subcutaneous and topical routes
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