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Although shedding data are rarely reported in clinical studies, available evidence suggests that MVA persists in the body for less than 48 hours, and detection of shed material in excreta is short-lived, consistent with rapid viral clearance due to MVAs replication-deficient properties, which mitigates concerns about environmental release or transmission to untreated individuals 75

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This dual-receptor pharmacology, GH release through GHSR1a and cardioprotection through CD36, gives GHRP-6 a therapeutic profile that newer, more selective secretagogues like ipamorelin do not possess