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2,3 In REDEFINE 1, adverse events were mainly gastrointestinal, (79.6% in the CagriSema group vs 39.9% with placebo) including nausea (55% vs 12.6%), constipation (30.7% vs 11.6%), and vomiting (26.1% vs 4.1%)
Biomech Model Mechanobiol (2017) 16(4):1295308
Dosage protocols used in preclinical research vary depending on the study design and research objectives
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doi: 10.1007/s10637-009-9302-0 87 JaganathanSKMandalM
