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They are not approved for human or animal use nor consumption by the Food and Drug Administration (FDA)

Cagrilintide monotherapy remains investigational, and the CagriSema combination although it has been submitted for regulatory review remained unapproved as of this writing

PMID: 4762237 Seiwerth S, et al

Regulatory approval status Cagrilintide is not currently FDA-approved as a standalone medication

However, because excessive copper exposure can be harmful, research protocols monitor total copper levels, especially in systemic studies

While cagrlintide and tirzepatide offer significant benefits, patients should be aware of potential side effects