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These studies, including work from Cornell University and other institutions researching metabolic syndrome, chose subcutaneous administration because it allows precise control over plasma pharmacokinetics
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In contrast, blood glucose level of 54 mg/dL or less occurred in 6% of patients receiving the 14 mg tablets, 3% of patients receiving placebo, and 0% of patients receiving the 7 mg tablets
The absence of IGF-1 stimulation is particularly relevant for long-term safety
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