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Jul 18, 2026
Metabolic
Also known as: AM833 Β· NNC0174-0833 Β· long-acting amylin analogue
A long-acting amylin analogue studied for weight management, mostly in combination with semaglutide. Human trial data are substantial but it is not yet approved anywhere.
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Cagrilintide is a long-acting synthetic analogue of amylin, a pancreatic hormone co-secreted with insulin that influences satiety and gastric emptying. It is being developed by Novo Nordisk for chronic weight management, primarily as a once-weekly combination with semaglutide known as CagriSema. It is an investigational drug, not an approved medicine.
A randomised phase 2 dose-finding trial (Lancet, 2021) reported dose-dependent weight reduction with cagrilintide monotherapy in people with overweight or obesity. The phase 3 REDEFINE 1 trial (NEJM, 2025) tested it combined with semaglutide and found clinically meaningful weight loss versus placebo. Cagrilintide alone is not approved, and long-term outcomes and safety of monotherapy are not established.
Across trials the most common adverse events were gastrointestinal (nausea, constipation, diarrhoea) and injection-site reactions. As an investigational product its full long-term safety profile is not established, and research-market material is not a quality-assured or pharmacist-dispensed medicine.
Investigational; not an approved medicine in the EU or US as of mid-2026. Developed by Novo Nordisk; the fixed combination with semaglutide (CagriSema) is under regulatory review. Investigational product, not a general-use compound.
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The table lists only product-specific offers that were checked and for which a real destination exists. Missing prices, quantities, stock and laboratory details are not inferred.
Documentation
Vendor-supplied data
COA stated as available
Not independently documented
Checked
Jul 18, 2026
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Cagrilintide is a long-acting synthetic analogue of amylin, a pancreatic hormone co-secreted with insulin that influences satiety and gastric emptying. It is being developed by Novo Nordisk for chronic weight management, primarily as a once-weekly combination with semaglutide known as CagriSema. It is an investigational drug, not an approved medicine.
Cagrilintide (also cataloged as AM833 or NNC0174-0833) is a long-acting synthetic analogue of amylin, a pancreatic hormone that is co-secreted with insulin and helps regulate satiety and the rate of gastric emptying. It is being developed by Novo Nordisk for chronic weight management, and it is studied most often not on its own but as a once-weekly fixed combination with the GLP-1 drug semaglutide, known as CagriSema. The single most important thing to understand about cagrilintide is that it is an investigational drug: it is not an approved medicine in the European Union, the United States, or elsewhere as of mid-2026.
The reason cagrilintide attracts serious attention is that, unlike many research-market peptides, it has a substantial human trial record. A randomized phase 2 dose-finding study (Lancet, 2021) reported dose-dependent weight reduction with cagrilintide used on its own in people with overweight or obesity, and the phase 3 REDEFINE 1 trial (NEJM, 2025) tested it combined with semaglutide and found clinically meaningful weight loss versus placebo. Its proposed mechanism β agonism of amylin and calcitonin receptors β sits on a well-characterized satiety-signalling pathway. Even so, cagrilintide on its own is not approved, and the long-term outcomes and safety of monotherapy are not established, which is why peptides.cx grades the evidence B rather than higher.
Across the trials, the most commonly reported adverse events were gastrointestinal β nausea, constipation, and diarrhoea β along with injection-site reactions. Because it remains an investigational product, its full long-term safety profile is not established, and material sold on the research market is not a quality-assured or pharmacist-dispensed medicine. The CagriSema combination is under regulatory review, but review is not approval, and nothing about that process changes cagrilintide's current status. This page is an educational reference summarizing what the science does and does not show; it is not medical advice, and it does not provide dosing, protocols, or sourcing guidance.
Evidence grade: B
A randomised phase 2 dose-finding trial (Lancet, 2021) reported dose-dependent weight reduction with cagrilintide monotherapy in people with overweight or obesity. The phase 3 REDEFINE 1 trial (NEJM, 2025) tested it combined with semaglutide and found clinically meaningful weight loss versus placebo. Cagrilintide alone is not approved, and long-term outcomes and safety of monotherapy are not established. Characterised in preclinical obesity models, where amylin-receptor agonism reduced food intake and body weight.
A randomised phase 2 dose-finding trial (Lancet, 2021) reported dose-dependent weight reduction with cagrilintide monotherapy in people with overweight or obesity. The phase 3 REDEFINE 1 trial (NEJM, 2025) tested it combined with semaglutide and found clinically meaningful weight loss versus placebo. Cagrilintide alone is not approved, and long-term outcomes and safety of monotherapy are not established.
Characterised in preclinical obesity models, where amylin-receptor agonism reduced food intake and body weight.
Across trials the most common adverse events were gastrointestinal (nausea, constipation, diarrhoea) and injection-site reactions. As an investigational product its full long-term safety profile is not established, and research-market material is not a quality-assured or pharmacist-dispensed medicine.
Investigational; not an approved medicine in the EU or US as of mid-2026. Developed by Novo Nordisk; the fixed combination with semaglutide (CagriSema) is under regulatory review. Investigational product, not a general-use compound.