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Peptides targeting metabolism, weight management, and body composition. Research in this category includes compounds affecting appetite regulation, fat oxidation, and metabolic rate.
Fat loss and metabolic peptides encompass a spectrum of compounds that target adipose tissue, appetite regulation, and metabolic signalling — from cutting-edge GLP-1 medications to research peptides with decades of preclinical data. This is one of the fastest-evolving areas in both pharmaceutical medicine and peptide research, driven by rising rates of obesity, type 2 diabetes, and metabolic syndrome globally.
Semaglutide and tirzepatide represent the licensed, pharmaceutically approved end of this spectrum. Semaglutide (Ozempic, Wegovy) is a GLP-1 receptor agonist that suppresses appetite through hypothalamic signalling, slows gastric emptying, and improves insulin sensitivity. In clinical trials, weekly semaglutide achieved 15-17% body weight reduction over 68 weeks. Tirzepatide (Mounjaro) adds GIP receptor agonism to GLP-1, producing a dual incretin effect that drives up to 22% weight loss in clinical studies — the highest efficacy of any approved anti-obesity medication.
AOD-9604 occupies a different niche within this category. A C-terminal fragment of human growth hormone (hGH176-191), AOD-9604 was developed to isolate the fat-metabolising effects of growth hormone without its growth-promoting or insulin-desensitising properties. Preclinical studies demonstrate direct stimulation of lipolysis in adipocytes and inhibition of lipogenesis. The US FDA granted AOD-9604 GRAS (Generally Recognised As Safe) status for use as a food ingredient, making it one of the few research peptides with formal safety designation.
In the UK, semaglutide and tirzepatide are MHRA-approved prescription medications available through NHS and private providers. NHS prescribing for weight management follows NICE guidelines (TA875, TA943) — patients typically require a BMI of 35+ with weight-related comorbidities for NHS access, though criteria are expanding. AOD-9604 and similar research peptides are unregulated and cannot be marketed as medicines.
Common research questions in this category include: optimising GLP-1 therapy for body composition rather than weight alone; mitigating muscle loss during rapid weight loss; combining appetite suppression with peripheral fat metabolism; and strategies for metabolic flexibility. Some online sources propose pairing licensed GLP-1 medicines with unlicensed peptides such as ipamorelin, CJC-1295, or tesamorelin to "preserve lean mass" — these combinations have no controlled human trial evidence in this context and Peptide Authority does not publish stacking protocols.
A modified fragment of human growth hormone specifically researched for its fat-metabolising properties without the growth-promoting effects of full HGH.
View detailsA GLP-1 receptor agonist approved for type 2 diabetes and obesity treatment, representing one of the most significant advances in weight management pharmacotherapy.
View detailsA triple monoamine reuptake inhibitor originally developed for neurological conditions, now researched for its potent effects on appetite suppression and weight loss.
View detailsA fragment of human growth hormone corresponding to amino acids 176-191, researched specifically for its fat-metabolising properties.
View detailsA naturally occurring gut hormone that regulates glucose metabolism and appetite, serving as the basis for major obesity and diabetes medications.
View detailsThe 'hunger hormone' that stimulates appetite and growth hormone release, with important roles in metabolism and energy balance.
View detailsA pancreatic hormone co-secreted with insulin that regulates glucose and appetite, the basis for the diabetes drug pramlintide.
View detailsA hormone produced by fat cells that regulates appetite, energy expenditure, and body weight.
View detailsA dual glucagon/GLP-1 receptor agonist under development by Boehringer Ingelheim, researched for its potential in weight management, metabolic health, and non-alcoholic steatohepatitis (NASH).
View detailsA long-acting amylin analogue developed by Novo Nordisk, researched for its role in appetite regulation, satiety signalling, and weight management, including as part of the CagriSema combination with semaglutide.
View detailsMonograph coming soon.
Monograph coming soon.
Monograph coming soon.