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For recovery enhancement, performance optimisation, or longevity goals in healthy people, until a randomised, placebo-controlled trial in a defined population with an objective primary endpoint and pharmacovigilance over a clinically meaningful duration produces data we do not currently have, we just don't have good evidence of benefit, let alone safety
Microdosing may be considered when standard starting doses create barriers to tolerance or continuation
The pharmacology of GLP-1, GIP, and glucagon based therapies has been the subject of decades of research
(PubMed) Gladyshev VN
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