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AEs leading to trial product discontinuation occurred in 2/62 (3%) participants in the CagriSema 2.4 mg/2.4 mg group, 2/63 (3%) participants in the CagriSema 1 mg/1 mg group, and 2/64 (3%) participants in the placebo group

It occurs in a variety of forms most of which are active within the body

These sources help ensure the fetus receives essential nutrients for growth and development

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Tolerability was reassuring, with gastrointestinal effects the most common adverse events and the majority rated mild to moderate, consistent with the wider GLP-1 class