Protocols · Skin & Anti-Aging · Epithalon
Research Protocol · Educational

Epithalon
Dosage Protocol

Epithalon is dosed once daily under the skin at a fixed dose, with no titration. For the 10 mg vial, the reconstitution math, the 20-day cycle, and syringe-unit conversions follow, with every figure sourced to the protocol guide and peer-reviewed literature cited below.

Epithalon
Epithalon · 10 mg · research use only
Fixed dose
5 mg/day × 20 days
Reconstitute
2.0 mL BAC water
Concentration
5.0 mg/mL
Storage
2–8 °C · 2–4 weeks
Dosage

Dosage Chart

Note on concentration. Unlike most 10 mg vials on this site, the Epithalon vial protocol reconstitutes to 5.0 mg/mL, not 3.33 mg/mL, because it uses 2.0 mL of bacteriostatic water instead of 3.0 mL. At this concentration, 1 unit on a U-100 syringe equals 50 mcg. [5]

Fixed dose, no titration: 5,000 mcg (5 mg) once daily for 20 consecutive days, preferably in the evening or at bedtime to align with natural melatonin rhythms. [5]

ProtocolDaily doseUnits (U-100)Volume
Days 1–205,000 mcg (5 mg)100 u1.00 mL

A 1.00 mL dose is the full volume of a standard 1 mL/100-unit syringe. Each 10 mg vial reconstituted this way yields approximately 2 doses at the standard 5 mg daily protocol, so a full 20-day cycle draws from about 10 vials. [5] Animal research (mice) used approximately 1.0 microgram per mouse, roughly 30–40 micrograms per kilogram; this rodent dosing is not a basis for the human protocol above and is included only as background. [1]

Prep

Reconstitution

10 mg vial, mixed to a working concentration before drawing a dose.

Add 2.0 mL of bacteriostatic water to the 10 mg vial to yield a final concentration of 5.0 mg/mL. [5]

Freeze the lyophilized vial at −20 °C in dry conditions before reconstitution. Once reconstituted, refrigerate at 2–8 °C and use within 2–4 weeks; avoid repeated freeze-thaw cycles. [5]

Mechanism

How It Works

Epithalon (also called Epitalon) is a synthetic tetrapeptide with the amino acid sequence Ala-Glu-Asp-Gly (AEDG) and molecular formula C14H22N4O9. It is a synthetic pineal tetrapeptide studied for proposed effects on telomere biology, telomerase activity, melatonin rhythm, and age-related mechanisms. [4]

A 2025 review reports that the peptide exerts a direct influence on melatonin synthesis, alters interleukin-2 mRNA levels, and enhances the activity of several enzymes, including telomerase. [1] In an in vitro mouse-oocyte model, epitalon at 0.1 mM concentration reduced intracellular reactive oxygen species, increased mitochondrial membrane potential and mitochondrial DNA copy number, and decreased apoptosis; this is a cell-model finding, not a human clinical result. [2] In a 2024 human biomarker study in elderly subjects, AEDG peptide application was associated with regulation of circadian-rhythm genes (Cry2, AANAT, ASMT, CLOCK) in buccal epithelium, alongside reduced expression of apoptosis-promoting proteins. [3]

Human evidence overall is limited and regionally concentrated, not strong enough to establish Epithalon as a general longevity or sleep treatment; preclinical evidence in cell and animal models is stronger than the clinical evidence. [4] Epithalon is not FDA-approved for general therapeutic, longevity, or sleep use. FDA records show an orphan-drug designation was filed for retinitis pigmentosa, but that indication's status is explicitly "Not FDA Approved for Orphan Indication," meaning the designation exists without the approval that would follow it. [4] The FDA has separately identified safety concerns for compounded Epithalon, including possible immunogenicity from aggregation and peptide-related impurities. [4] A sleep/insomnia application was scheduled for FDA discussion in July 2026 but remains unapproved. [4] This section describes what the cited literature reports; it is not a claim of safety or effectiveness for human use.

Evidence

References

Educational use only. This content is for research and educational purposes only and is not medical advice, diagnosis, or treatment. Epithalon is not FDA-approved for any indication; its orphan-drug designation for retinitis pigmentosa has not resulted in FDA approval. Human clinical evidence is limited and preclinical evidence is stronger than clinical evidence. It is for research use only and is not intended for human consumption. Clinical decisions should involve a qualified healthcare provider.