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Key safety observations from Phase 2 data include: Gastrointestinal side effects were the most commonly reported adverse events Dose-dependent tolerability issues were noted, particularly at higher doses, with meaningful discontinuation rates Increases in heart rate were observed, consistent with the known class effect of GLP-1 receptor agonists
Inject subcutaneously in the stomach (abdomen), thigh, or upper arm, and make sure to change the injection site with each dose
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