Weight & metabolic

Cagrilintide

AM833

Phase 3 trialsEvidence: Human trialsPeptide analogueLimited human data

Cagrilintide is a long-acting amylin analogue developed by Novo Nordisk. It is the amylin component of CagriSema and is also under investigation as a single agent for weight management. It is not approved as a standalone product.

Also known as: AM 833

Status
Cagrilintide is in Phase 3 clinical trials and not approved.
Evidence
Human trials. Published clinical trials in people report results.
Half-life
Approximately 7 to 8 days, consistent with once-weekly dosing.
How it's taken
Once-weekly subcutaneous injection (investigational)
Mechanism
Incretin (GLP-1 / GIP / glucagon / amylin)
Pathways
Amylin

How Cagrilintide works

Cagrilintide is a modified, acylated analogue of human amylin, a hormone co-secreted with insulin by pancreatic beta cells. It acts at amylin and calcitonin receptors in the area postrema and hypothalamus to slow gastric emptying, suppress post-meal glucagon secretion and increase satiety. The mechanism is distinct from and complementary to GLP-1 agonism, which is the rationale for combining the two.

What research has looked at

Evidence level: Human trials. Published clinical trials in people report results. These are areas studied or reported, not promised effects.

Reported side effects and risks

Sources

  1. PubMed research on cagrilintide amylin analogue CagriSema · NIH · National Library of Medicine
  2. DrugBank record for cagrilintide · DrugBank
  3. Active clinical trials for cagrilintide · U.S. National Library of Medicine

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Cagrilintide FAQ

What is Cagrilintide?

Cagrilintide is a long-acting amylin analogue developed by Novo Nordisk. It is the amylin component of CagriSema and is also under investigation as a single agent for weight management. It is not approved as a standalone product.

How does Cagrilintide work?

Cagrilintide is a modified, acylated analogue of human amylin, a hormone co-secreted with insulin by pancreatic beta cells. It acts at amylin and calcitonin receptors in the area postrema and hypothalamus to slow gastric emptying, suppress post-meal glucagon secretion and increase satiety. The mechanism is distinct from and complementary to GLP-1 agonism, which is the rationale for combining the two.

Is Cagrilintide FDA approved?

No. Cagrilintide is in Phase 3 clinical trials and not approved. Evidence level: human trials. Published clinical trials in people report results.

What is the half-life of Cagrilintide?

Reported half-life: Approximately 7 to 8 days, consistent with once-weekly dosing.

How is Cagrilintide taken?

Once-weekly subcutaneous injection (investigational).

What side effects have been reported with Cagrilintide?

Reported in the sources: Gastrointestinal effects including nausea, vomiting and constipation, consistent with delayed gastric emptying; Injection-site reactions; As an investigational agent, its long-term safety profile is not established, and no regulator has approved it as a single agent; Material sold outside a clinical trial is not a regulated pharmaceutical product and its identity, purity and dose accuracy are unverified.

Educational summary compiled from the sources listed above. Not medical advice. Peptide Vault does not sell, source or recommend any compound. Talk to a qualified clinician before starting or changing anything.