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Investigational and not approved by the FDA. This page is educational information only. It is not medical advice and not a recommendation to use anything.
IndexedBuilt automatically from public databases on 2026-09-30. Not yet hand-reviewed by PLOBT.How this works →

CagriSema

Investigational

Amylin and GLP-1 combination

Also known as: cagrilintide/semaglutide, Cagrilintide + Semaglutide, Semaglutide + Cagrilintide, Cagri-Sema, CagriSema 2.4

Evidence score
56/ 100
Moderate evidence

A real evidence base, with gaps

  • Regulatory standing. In clinical trials, not yet approved
  • Limited human data. Some human data exists, not conclusive
  • Registered human trials. 31 registered studies on ClinicalTrials.gov, most advanced Phase 3
  • No sources. Nothing cited to verify

Computed with the same four public criteria as every profile. The human-evidence grade on an indexed profile is set automatically and may change when it is hand-reviewed. It is not a safety score, not a purity rating, and not medical advice, and not a claim that this compound treats, cures, or prevents any condition.

What it is

CagriSema is an investigational fixed combination of cagrilintide, a long-acting amylin analogue, and semaglutide, a GLP-1 receptor agonist. The two components are thought to act on complementary appetite and satiety pathways, with amylin signaling and GLP-1 signaling both influencing food intake, gastric emptying, and blood sugar regulation.

What the evidence shows

Automatic summaryLimited human data

CagriSema is not FDA-approved; it has been studied in about 31 registered human trials reaching Phase 3, with published results reporting weight and glucose effects in people with obesity or type 2 diabetes. Its long-term safety and effectiveness have not been established through regulatory review, and it remains investigational.

Registered human trials

Published literature

Sources

Risks, side effects and study doses are only published on hand-reviewed profiles. Want this one reviewed, or spotted something wrong? Tell us.