Now reading Entry 025 / 102 Last revised Sep 28, 2026 11 sources 3 comparisons Methodology →
A specimen of the Longevity drawer Drawer D · Longevity

Epithalon

Research Only

Epitalon (Ala-Glu-Asp-Gly, AEDG) has produced telomere-related changes in cultured human cells, including a 2025 independent laboratory report. Those experiments do not show longer human life or safe clinical use; controlled human efficacy and exposure data remain unavailable.

Epitalon · Epithalone · AEDG peptide

Research evidence
Low

Cell and animal findings; no administered-human efficacy study among the cited works.

Preclinical
73%
Human research
0%

Based on 11 cited sources

11 visible records: nine publications, one FDA record and one published correction. Eight original preclinical papers include treated human cells, not treated patients. The correction is a separate record, not an additional experiment.

!
Evidence Level
low
Not currently in FDA's Category 2; FDA records the nomination of "Epitalon" as withdrawn by the nominator (FDA, "Certain Bulk Drug Substances for Use in Compounding that May Present Significant Safety Risks"; page content current as of 22 April 2026).
Research Only
Identity
SCALE · 1:1 N-TERMINUS C-TERMINUS 4 AA · 390.35 Da
Also Known As
Epitalon • Epithalone • AEDG peptide
Class
Tetrapeptide
Length
4 amino acids
Mol. weight
390.35 Da
Sequence
AEDG
Molecular Structure
A
E
D
G
Hydrophobic
Polar
Positive
Negative

Epitalon, also called Epithalon, is the synthetic Ala-Glu-Asp-Gly (AEDG) tetrapeptide. It is distinct from pineal extracts and from other peptide bioregulators. Its best-cited telomere results come from cultured cells, not from treated people.

Telomere experiments

A 2003 study reported telomerase activity and telomere elongation after adding AEDG to telomerase-negative human fetal fibroblast cultures. A 2025 independent study reported hTERT/telomerase-associated telomere lengthening in normal cultured human cells and alternative-lengthening-of-telomeres activity in breast-cancer cell lines. The latter observation raises a mechanistic safety question; it does not prove an increase in cancer risk in humans. A published correction replaced incorrect Figures 1–3 in the 2025 paper; the corrected figures should be used when appraising its results. Neither study establishes longer lifespan, improved sleep or clinical benefit. PMID:12937682 · PMID:40908429 · Correction

Earlier animal and experimental work on chromatin, pineal-related and antioxidant measures is hypothesis-generating. It cannot be turned into a human anti-aging timeline or a claim that AEDG safely activates telomerase in a whole person. Studies of cultured human cells are preclinical studies, not human treatment trials.

Human evidence and safety boundary

No controlled human efficacy study showing improved lifespan, healthspan or sleep was identified. FDA’s compounding review reports insufficient safety-related information for the proposed administration route and cites potential immunogenicity from aggregation and peptide-related impurities. Combination effects with other peptides are unknown. FDA compounding safety review

i. Telomerase Activation Pathway · Cultured-Cell Telomeres
EpithalonEpigenetic ModulationhTERT Gene Transcription ↑Telomerase Reverse Transcriptase (TERT) ↑Telomerase Enzyme AssemblyTelomere-length change in cultured cells
ii. Chromatin Remodeling Pathway · Gene Expression
EpithalonHistone Interactions (H1, H2b, H3, H4)Heterochromatin DecondensationExperimental chromatin and gene-expression changes
Mechanism hTERT gene transcription activation leading to telomerase enzyme assembly
Supported 2 direct studies
Benefit appears to affect telomere-related measures in cultured cells
Evidence Level
Low
2 In Vitro
Mechanism Epigenetic modulation of chromatin structure via histone interactions
Emerging 2 direct studies
Benefit suggested to alter gene expression in experimental models
Evidence Level
Very Low
2 In Vitro
Mechanism Pineal gland stimulation increasing melatonin synthesis
Emerging 1 direct study
Benefit may affect pineal-related markers in preclinical models
Evidence Level
Very Low
1 Animal
Mechanism Upregulation of antioxidant enzymes (SOD, glutathione peroxidase)
Emerging 2 direct studies
Benefit may reduce oxidative stress markers
Evidence Level
Very Low
2 Animal
Mechanism Confidence
Established
Supported
Emerging
Evidence Level
High
Moderate
Low
Very Low

This dossier synthesizes available evidence from peer-reviewed literature, regulatory documents, and clinical trial registries. Evidence strength labels summarize the cited material for this entry and should be read alongside its population, model, and study limitations.

For complete methodology details, see our Methodology page.

Important Disclaimer

This dossier is for educational purposes only and does not constitute medical advice. Always consult a qualified healthcare provider before making health decisions.

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Compare Epithalon

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Safety profile Epithalon: adverse events, contraindications and monitoring →

Compared With

23 comparisons

Conditions Studied

4 entries

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