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This is not by itself disqualifying many compounds begin life in a single laboratory but external replication is the standard the literature has not yet met for the VEGFR2/eNOS mechanism or the rodent connective-tissue effect sizes

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Its less invasive than injections, making it a preferred choice for scenarios where participant comfort and simplicity are primary considerations in 2026

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It has a very short half-life, requiring frequent (often daily) injections to maintain elevated GH pulses [3][4]