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In the phase 2 trial, 41% to 63% of participants receiving cagrilintide (0.3 to 4.5 mg) experienced gastrointestinal adverse events, compared to 32% with placebo

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Corts-Albornoz MC, Garca-Guqueta DP, Velez-van-Meerbeke A, Talero-Gutirrez C

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