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Description

Source data are provided with this paper

QA/RA managers need to take standard steps when tracking the risk of pancreatitis and evaluating thyroid C-cell tumors (based on data from rodents)

Dihexa is not approved by the FDA or EMA

The animals were group-housed until one week before treatment initiation, after which they were given daily subcutaneous injections of vehicle or Cagrilintide at doses of 0.3, 3, or 30 nmol/kg for 21 days