Also called: Cagrilintide UK & Lab UK, Cagrilintide and Semaglutide
Cagrilintide is a lab-made medicine that copies a natural body chemical called amylin. Amylin helps control hunger and blood sugar after meals. It is being studied as a weight-loss treatment for people with obesity. Right now it is not sold as an approved medicine.
In studies, cagrilintide works by turning on two tiny parts of cells called the amylin and calcitonin receptors. Turning these on helps the brain feel full, so animals and people eat less food. In animal tests it lowered body weight and also improved blood fats and insulin levels. Scientists think it may help treat obesity in the future.
There is still a lot we do not know. Most published findings so far come from animal studies, and results in rats do not always match what happens in people. Cagrilintide is not approved by drug regulators, so its safety and long-term effects in humans are still being checked in clinical trials. People should not use it outside of a supervised research or medical setting.
Benefits
The benefits people report — backed by research.
You just read the research on Cagrilintide. The cheat-sheet maps the most-used peptide stacks — doses, timing, and what to check before buying — on one page.
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1 reported routine — each line links to the source it came from.
From published sources
Routines as reported in peer-reviewed papers, clinical guidance, or vetted media — each linked to the source it came from.
SubQ
mg vs mcg: one milligram (mg) equals 1,000 micrograms (mcg) — multiply by 1,000 going from mg to mcg, divide by 1,000 going from mcg to mg. Mixing the two up is a thousand-fold dosing error: 1 mg taken instead of 1 mcg is a 1,000× overdose; 1 mcg instead of 1 mg is a 1,000× underdose. Always double-check the unit label and the decimal place.
Safety
Adverse effects reported in the research and by community use.
Reported in research and community sources — not exhaustive. Discontinue use and consult a healthcare professional if side effects occur.
Compare research-grade suppliers with third-party COAs and published purity data. For in-vitro and laboratory research use only — not for human consumption, diagnosis, or treatment.
Timeline
Key moments in Cagrilintide’s research and regulatory timeline — sourced and dated.
News
Dated, sourced reporting that mentions Cagrilintide.
Novo Nordisk announced topline results showing CagriSema, a fixed-dose combination of cagrilintide and semaglutide, produced greater weight loss than tirzepatide in adults with type 2 diabetes in the REIMAGINE 5 trial (12.4% vs. 9.1% at 60 weeks), while achieving noninferior HbA1c reductions. In the REDEFINE 9 trial, CagriSema led to 21% weight loss at 68 weeks in adults with overweight or obesity without diabetes. These are topline company-announced results from ongoing trial programs.
A systematic review and network meta-analysis of 39 studies (33,354 participants) assessed gastrointestinal adverse events of GLP-1 receptor agonists in non-diabetic patients with overweight or obesity. Nausea, vomiting, diarrhea, and constipation were the most common side effects. Orforglipron showed the highest nausea risk, followed by exenatide, tirzepatide, semaglutide, and liraglutide. The differing safety profiles can help clinicians tailor weight-loss therapy choices.
Novo Nordisk's experimental combination therapy CagriSema demonstrated superior weight loss and blood sugar control compared to semaglutide alone in a Phase 3 trial. The drug combines the GLP-1 agonist semaglutide with cagrilintide, an amylin receptor agonist, resulting in a 14.2% reduction in body weight over 68 weeks. These results suggest a potential new standard for treating type 2 diabetes and obesity.
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