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Epub 2015 Apr 10

1 In the REIMAGINE 2 trial, the most commonly reported AEs were GI-related, occurring in 405/603 (67.2%) participants in the CagriSema 2.4 mg/2.4 mg group, 326/605 (53.9%) participants in the semaglutide 2.4 mg group, 60/152 (39.5%) participants in the cagrilintide 2.4 mg group, 329/594 (55.4%) participants in the CagriSema 1 mg/1 mg group, 288/608 (47.4%) participants in the semaglutide 1 mg group, and 42/149 (28.2%) participants in the placebo group

We've generally chosen the opposite

These effects are typically transient and resolve within hours to days

(This would apply to any of the six peptides discussed in the meeting.) Any clinics currently claiming the peptide is FDA approved or fully cleared for commercial human use are making legally false statements