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Epithalon is administered in defined cycles of ten to twenty days with rest periods between them, responding to pulse-dosing rather than continuous daily administration due to its mechanism of telomere regulation and circadian rhythm modulation

3A, a substantial ten-fold increase in ALT activity was observed for 21NT after treatment with epitalon when compared with the untreated control

Dihexa, with its combined N-hexanoic-Tyr-Ile-(6) aminohexanoic amide structure, exhibited a significantly extended half-life of 335.5 9.5 min, confirming that both N- and C-terminal modifications are effective strategies for improving metabolic stability [1]

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