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Gastrointestinal adverse events occurred in approximately 79.6% of CagriSema patients versus about 40% with placebo

Subcutaneous administration suffers from: Lower bioavailability Variable absorption Different pharmacokinetics Which means the systemic exposure of DSIP via subcutaneous administration is not equivalent to what is achieved with intravenous infusion

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6b we calculated rBFI values for early and late gates
