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BMC Cancer 16: 474, 2016

The safety profile of cagrilintide, as observed in clinical trials , is primarily characterized by gastrointestinal disturbances , most notably mild to moderate nausea during the initial titration phase

Working concentrations vary widely across published protocols depending on whether the study is in-vitro, animal, or topical, so researchers should set concentration to their own study design

Consider whether the commitment makes sense given that your tolerance and results are somewhat unpredictable when starting treatment

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