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IGF-1 LR3 is not approved by the FDA for human or veterinary use
Missed dose management requires careful consideration to maintain therapeutic efficacy while avoiding adverse effects from irregular dosing
In a contemporary cohort of 16,492 patients with T2D and at high/very high CV risk participating in the SAVOR-TIMI 53 trial [6], CVD remained the leading cause of death and approximately one-third of all deaths were classified as sudden
Studies have shown increased fat oxidation and energy expenditure following administration
Ongoing studies continue evaluating long-term safety, including digestive health, gallbladder events, pancreatitis risk, hydration, nutrition, and overall tolerability
doi: 10.1016/S2213-8587(21)00002-4 3 BellisSAKuhnIAdamsSMullarkeyLHollandA
