Cagrilintide
Also known as: AM833, cagri
An investigational long-acting amylin analog — interesting on its own in phase 2, but its real momentum is as the partner to semaglutide in the CagriSema combination.
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Not a GLP-1 at all — an amylin analog, a different appetite-regulating mechanism — which is exactly why it is being paired with semaglutide rather than competing with it. On its own it produced roughly 10% weight loss in a phase 2 dose-finding trial; combined with semaglutide as CagriSema the numbers go higher. Still investigational, not approved, and its standalone case is weaker than its combination case. Note one real distinction: as an amylin analog it does not carry the GLP-1 class thyroid boxed warning.
Key finding: Up to ~10.8% mean body-weight reduction at 2.4 mg/week over 26 weeks (phase 2 dose-finding, Lau 2021)
Mechanism
Cagrilintide is a long-acting analog of amylin, a hormone co-secreted with insulin by pancreatic beta cells. Amylin promotes satiety, slows gastric emptying, and suppresses glucagon — an appetite-regulation route that is mechanistically distinct from the GLP-1/GIP incretin pathway. That distinction is the whole point of the program: because amylin and GLP-1 reduce appetite through different signaling, combining cagrilintide with semaglutide (the CagriSema combination) is expected to be additive rather than redundant. Engineered for once-weekly dosing to match its semaglutide partner.
What the research shows
Two phase 2 readouts anchor this. As a standalone agent, the dose-finding trial (Lau et al., 2021, Lancet) gave cagrilintide across a dose range in people with overweight or obesity; the top 2.4 mg dose produced roughly 10.8% mean weight loss over 26 weeks, with a liraglutide 3.0 mg active comparator in the same trial. That is respectable but not class-leading on its own. The more consequential data are combinational: in a phase 2 trial in type 2 diabetes (Frías et al., 2023, Lancet), CagriSema — cagrilintide 2.4 mg plus semaglutide 2.4 mg — drove larger weight and glycemic reductions than either component, which is the basis for the larger phase 3 program. Bottom line: as a solo drug the evidence is early and middling; as half of CagriSema it is one of the more interesting bets in the pipeline. Either way it is investigational, not approved.
Benefits studied
- Up to ~10.8% mean weight loss as monotherapy at 2.4 mg over 26 weeks (phase 2)
- Larger weight and glycemic reductions when combined with semaglutide as CagriSema (phase 2, type 2 diabetes)
- Amylin mechanism is complementary to GLP-1, supporting the combination rationale
- Once-weekly dosing compatible with its semaglutide partner
Risks & unknowns
- Not approved by any regulator — investigational, phase 2 only; long-term safety is unknown
- GI effects (nausea, vomiting) are the most common adverse events, as across appetite-suppressing agents
- Injection-site reactions reported in the dose-finding trial
- As an amylin analog it does not carry the GLP-1 class thyroid C-cell boxed warning — but the absence of that specific warning is not evidence of long-term safety, which remains untested
- Most of the compelling data are combinational (CagriSema); standalone evidence is thinner
- Investigational prescription-grade drug — sourcing outside a trial or licensed clinician is unsafe and outside any legal channel
Regulatory status
In clinical trials. Under active investigation in human trials; not yet approved.
Goals studied: Fat loss, Body composition
FAQ
- Is cagrilintide a GLP-1 drug?
- No. It is an amylin analog — a different appetite-regulating hormone pathway. That is precisely why it is being combined with the GLP-1 agonist semaglutide rather than positioned against it; the two mechanisms are complementary.
- What is CagriSema?
- CagriSema is the investigational fixed combination of cagrilintide and semaglutide. The idea is that pairing an amylin analog with a GLP-1 agonist suppresses appetite through two routes at once, producing more weight loss than either alone. It is in late-stage trials but not approved.
- Can I buy cagrilintide now?
- Not legitimately. It is an investigational compound with no regulatory approval, available only within clinical trials. Anything sold as cagrilintide on the research-chemical market is unverified and outside the legal and safety framework.
Sources
- [1]Once-weekly cagrilintide for weight management in people with overweight and obesity: a multicentre, randomised, double-blind, placebo-controlled and active-controlled, dose-finding phase 2 trial
Lau DCW, Erichsen L, Francisco AM, Satylganova A, le Roux CW, McGowan BM, Pedersen SD, Pietiläinen KH, Rubino DM, Batterham RL · Lancet · 2021 · PMID 34798060 · model: human
Phase 2 dose-finding RCT in overweight or obesity where cagrilintide produced up to ~10.8% mean weight loss at 2.4 mg over 26 weeks, with a liraglutide 3.0 mg active comparator.
- [2]Efficacy and safety of co-administered once-weekly cagrilintide 2·4 mg with once-weekly semaglutide 2·4 mg in type 2 diabetes: a multicentre, randomised, double-blind, active-controlled, phase 2 trial
Frias JP, Deenadayalan S, Erichsen L, Knop FK, Lingvay I, Macura S, Mathieu C, Pedersen SD, Davies M · Lancet · 2023 · PMID 37364590 · model: human
Phase 2 RCT in type 2 diabetes showing the CagriSema combination (cagrilintide plus semaglutide, each 2.4 mg) produced greater weight and glycemic reductions than either agent alone.