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Its oral bioavailability makes it practical for long-duration rodent feeding studies and Phase II clinical trials in conditions such as GH-deficient adults, hip fracture recovery models, and age-related sarcopenia research

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Based on this evidence, it is recommended that long-term pharmacological management prioritize the optimization of treatment timing, formulation of personalized dosing regimens, and implementation of systematic efficacy monitoring and adverse reaction assessment protocols, to maximize therapeutic benefits while minimizing potential risks

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