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The most commonly reported adverse events in the Phase 2 trial were gastrointestinal in nature, including nausea, vomiting, and diarrhoea consistent with the GLP-1 receptor agonist class
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These correlations were then repeated for change in body weight and change in BTMs (CTX and P1NP)
Data are limited, the risk is theoretical and requires thorough investigation prior to administration in individuals attempting conception
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