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Perreault, L

Moreover, Li et al

Most Common Adverse Events Key Observations: Gastrointestinal adverse events are dose-dependent and most pronounced during dose escalation Symptoms typically peak within the first 4-8 weeks and diminish with continued treatment as tolerance develops Slow titration (4-week intervals) significantly reduces the incidence and severity of GI events Most adverse events classified as mild to moderate in severity [9] Discontinuation Rates 7.3% Placebo discontinuation rate [9] 15.8% Cagrilintide 2.4 mg (optimal dose) [9] 24.5% Cagrilintide 4.5 mg (high dose) [9] The majority of discontinuations due to adverse events occurred during the titration phase, with GI symptoms (nausea, vomiting) being the primary reasons

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To determine if you are a suitable candidate for tesofensine or a GLP-1 agonist, consult with your healthcare provider

Possible Risks Potential concerns associated with research peptides may include hormonal effects, unexpected tissue responses, contamination, incorrect dosing, and unknown long-term biological impact