What it is
Cagrilintide is a long-acting analogue of amylin, a hormone the pancreas releases at the same time as insulin. Amylin's job is to signal fullness and to slow how quickly the stomach empties.
The natural hormone is short-lived and awkward to work with. Cagrilintide is engineered to survive long enough for a once-weekly injection.
Why it is nearly always discussed alongside semaglutide
Because that is how it has been tested.
The compound most of the attention is really about is CagriSema — cagrilintide and semaglutide combined in one weekly injection. The two work on different systems: semaglutide on the GLP-1 pathway, cagrilintide on the amylin pathway. The reasoning for combining them is that two separate signals of fullness might do more than one.
This matters for reading anything written about cagrilintide. The striking numbers people quote come from trials of the combination. They describe what two drugs did together.
What the trials showed
This is one of the better-evidenced entries in this library, and worth stating precisely.
REDEFINE 1, in adults with overweight or obesity: an estimated 20.4% reduction in body weight at 68 weeks on cagrilintide-semaglutide, against 3.0% on placebo — a difference of 17.3 percentage points.
REDEFINE 2, in adults with obesity and type 2 diabetes: 13.7% against 3.4% on placebo. Among the treated group, 73.5% reached a glycated haemoglobin of 6.5% or less, against 15.9% on placebo.
These are large randomised phase 3 trials in people. Nothing in this library that is sold as a research chemical has evidence of this kind behind it.
The cost, in the same trials
Gastrointestinal side effects were reported by 72.5% of the treated group in REDEFINE 1, against 34.4% on placebo. The trials describe most as transient and mild or moderate.
Roughly three in four people getting nausea, vomiting or diarrhoea is not a footnote. It is the single most common reason people stop taking drugs in this class, and it belongs in the same paragraph as the weight-loss figure rather than several paragraphs below it.
Where it stands
Approved as a medicine: no. Completing large trials and being approved are different things, and a compound can finish phase 3 without ever being approved.
Sold as: a research chemical, by vendors who are not the trial sponsor. What is in those vials has not been through any of the manufacturing controls the trial product went through.
For the neighbouring approach — adding a second receptor to one molecule rather than pairing two drugs — see survodutide and the GLP-1/glucagon dual agonist mazdutide.
Last checked
2026-09-07.
