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The IGF-1 LR3 research community uses the same rule set, with the additional precaution of avoiding pre-bed dosing because of overnight hypoglycemia risk
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Furthermore, it reduces hepatic gluconeogenesis by improving insulin resistance, further relieving liver fat accumulation
Because AOD-9604 does not activate growth hormone receptors and functions through an entirely separate beta-3 adrenergic pathway, it does not trigger cortisol release
Animal studies show no toxicity even at doses 1,000 higher than typical use, but that doesn't mean high doses are risk-free in humans (Sikiric et al., 2014)
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