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The initial twice-daily formulation was discontinued due to exceptionally high rates of gastrointestinal adverse events (nausea and vomiting), leading to discontinuation rates exceeding 50% in trials

0.03) mg/L ( p = 0.01) but not by metformin/placebo, and with no significant difference between treatments

Is it necessary to adjust Ipamorelin dosage based on subject age or metabolic status in research models