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GLP-1/GIP/Glucagon Triple Agonist
Retatrutide is a next-generation triple agonist targeting GLP-1, GIP, and glucagon receptors simultaneously. This 39-amino acid peptide with C18 fatty diacid conjugation represents the cutting edge of metabolic peptide research. It has demonstrated exceptional results in adiposity reduction in preclinical and clinical studies.
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Retatrutide is a next-generation triple agonist targeting GLP-1, GIP, and glucagon receptors simultaneously. This 39-amino acid peptide with C18 fatty diacid conjugation represents the cutting edge of metabolic peptide research. It has demonstrated exceptional results in adiposity reduction in preclinical and clinical studies.
Tyr-Aib-Glu-Gly-Thr-Phe-Thr-Ser-Asp-Tyr-Ser-Ile-Ala-Leu-Asp-Lys-Ile-Ala-Gln-Gln-Asp-Phe-Val-Asn-Trp-Leu-Leu-Ala-Gln-Lys-Gly-Lys-Lys-Asn-Asp-Trp-Lys-His-Asn-Ile-Thr-Gln-NH₂
Tyr-Aib-Glu-Gly-Thr-Phe-Thr-Ser-Asp-Tyr-Ser-Ile-Ala-Leu-Asp-Lys-Ile-Ala-Gln-Gln-Asp-Phe-Val-Asn-Trp-Leu-Leu-Ala-Gln-Lys-Gly-Lys-Lys-Asn-Asp-Trp-Lys-His-Asn-Ile-Thr-Gln-NH₂
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Peer-reviewed scientific literature on Retatrutide from PubMed, NEJM, The Lancet, and other authoritative sources.
Jastreboff AM, Kaplan LM, Frías JP, et al.
New England Journal of Medicine, 389: 514–526 (2023)
Retatrutide 12 mg produced a reported measurable body-weight changes in clinical metabolic research settings
Müller TD, Finan B, Clemmensen C, et al.
Nature Reviews Endocrinology, 13: 728–749 (2017)
Glucagon receptor activation synergizes with GLP-1 and GIP pathways to enhance energy expenditure, reduce hepatic steatosis, and promote greater adiposity reduction than dual incretin agonism alone.