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Epithalon

Epithalon (Epitalon / AEDG Peptide)

LongevityTelomere supportSleepAnti-aging4 amino acids

What it is

A synthetic tetrapeptide with the sequence Ala-Glu-Asp-Gly (AEDG), developed by Vladimir Khavinson at the St. Petersburg Institute of Bioregulation and Gerontology as a synthetic analog of epithalamin, a crude bovine pineal gland extract. Epithalon has been studied primarily for its observed effects on telomerase activation, telomere elongation, melatonin rhythm restoration, and lifespan extension in animal models. Approximately 110+ publications exist, with nearly all originating from Khavinson's research group. No independent replication of key findings has been published, and no formal pharmacokinetic studies exist. The FDA placed epithalon on the Category 2 bulk drug substance list in September 2024, barring pharmacy compounding.

Community-reported ranges

Dosing ranges sourced from Khavinson's published clinical protocols and community forums. Nearly all primary research originates from a single laboratory. This is not dosing guidance.

Reported dose range

500010000 mcg

Estimated half-life

Unknown (estimated minutes)

Source: no formal PK studies; estimate based on small peptide pharmacokinetics

Reported cycle length

23 weeks on

16-26 weeks off

Route

subcutaneous, intramuscular

Common vial sizes

10mg, 50mg

Reported timing

PM (evening preferred due to melatonin-related effects)

Reported frequency

1x daily for 10-20 day cycles

Frequently discussed alongside

Based on community forum discussions. Not a recommendation to combine compounds.

Published research

The landmark 2003 study by Khavinson et al. demonstrated that epithalon induced telomerase expression and telomere elongation in telomerase-negative human fetal fibroblasts, with treated cells exceeding the Hayflick limit. Animal lifespan studies by Anisimov et al. showed mean lifespan increases of 11–31% across Drosophila, SHR mice, C3H/Sn mice, and LIO rats. In HER-2/neu transgenic mice, epithalon prolonged average lifespan by 13.5% and was observed to suppress breast adenocarcinoma development. Limited human data includes a prospective cohort of 266 elderly adults treated with epithalamin for 2–3 years. A critical caveat noted by the Alzheimer's Drug Discovery Foundation: nearly all studies originate from Khavinson's group with no independent replication. No formal pharmacokinetic data have been published.

Reported side effects

From community self-reports. Not from controlled studies.

No serious adverse events have been reported in available clinical studies, including trials with up to 12-year follow-up from Khavinson's group. Community users have reported injection site reactions, drowsiness (likely melatonin-related), vivid dreams, mild headaches, and occasional dizziness. A theoretical concern exists regarding telomerase activation and cancer promotion, though animal studies paradoxically showed anti-tumor effects. Systematic safety data from independent groups does not exist.

Regulatory status

FDA (United States)

Not approved. Placed on FDA Category 2 Bulk Drug Substance list in September 2024, prohibiting 503A and 503B pharmacy compounding. FDA cited immunogenicity concerns.

Health Canada

Not authorized as a therapeutic product. No DIN assigned. Classified as an unapproved new substance.

WADA (Competitive Athletes)

Not specifically named on the WADA Prohibited List, but effectively prohibited under category S0 (Non-Approved Substances), which bans any pharmacological substance not approved by any governmental regulatory authority for human therapeutic use.

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