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Description
Because GLP-3 (Reta) is an unapproved investigational molecule, it is not eligible for pharmacy compounding for human use
These effects are typically dose-related and diminish over the first 4-8 weeks of treatment

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), with 94% homology to human GLP-1, were approved in 2019 as the first GLP-1R agonists for oral administration (Ke et al., 2024) (Table 2)
Conclusion In conclusion, the preclinical and clinical studies demonstrated that GLP-1RAs and SGLT-2is act directly or indirectly on their receptors by crossing the BBB
The maximum recommended dosage is 2 mg per week
