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[2] [11] As of 2026, retatrutide has not received marketing authorisation from the Medicines and Healthcare products Regulatory Agency (MHRA) or the European Medicines Agency (EMA), and it remains an experimental compound available only within authorised clinical trial settings

Se ha observado que la mayora de los efectos gastrointestinales disminuyen con la exposicin continuada y la titulacin gradual de la dosis

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J Biol Chem 272:2760527611 [DOI] [PubMed] [Google Scholar] Kovoor A, Celver JP, Wu A, Chavkin C