Crystagen, product photo
Bioregulators

Crystagen

Khavinson bioregulator for the immune system. Tetrapeptide with research application in thymus function models.

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At a glance

Crystagen by the numbers

The key figures from our lexicon.

Full lexicon entry
Class
Short bioregulator peptide

Khavinson cytogen

Use
Subcutaneous

in mg

Sizes
20 mg

1 size in the shop

For research and educational purposes only. Values from the TPD lexicon, sources linked there.

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Knowledge

Everything about Crystagen

Description

Crystagen (Lys-Glu-Asp-Pro) is a synthetic tetrapeptide of the Khavinson bioregulator class with tissue-specific action on the immune system, particularly the thymus-mediated immune response. The substance was developed at the St. Petersburg Institute.

Per study reports Crystagen modulates gene expression in thymocytes and T lymphocytes via the Khavinson epigenetic mechanism. Preclinical studies describe effects on T cell maturation, cytokine profiles and age-related immune reactivity.

In Russian research literature Crystagen is often used in aging immunology setups - age-related thymus involution is one of the best-characterized aging mechanisms. Crystagen is described as bioregulator for restoring thymus function.

Typical application is subcutaneous in 10-20 day courses two to three times per year.

You can order Crystagen as lyophilized peptide in 10-pack at 20mg per vial.

This information is for research and educational purposes only. No medical recommendations.

Risks & Safety

Crystagen is classified as very mild in the available literature and is among the most well tolerated compounds of the Khavinson bioregulator class. In the available preclinical and limited human studies, no relevant toxic effects have been documented.

Observed in research and reports:

  • Injection site: mild redness or transient irritation with subcutaneous use is the most common observation. The tetrapeptide itself is considered low-reactivity.
  • Very thin human data: the data base consists almost entirely of small, Russian-language studies from the Khavinson environment. Independent peer-reviewed replication and robust long-term data on immunological use are absent.
  • Course-based pattern: the use described occurs in short 10-20 day courses. No data exist on the safety profile of continuous administration.

This classification does not replace medical advice. Risk and responsibility for any actual use lie entirely with the buyer.

Studies

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FAQ

Frequently asked

Sources for every answer: lexicon entry

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Is Crystagen approved or studied in humans?

It is not approved and as of 26 October 2026 the registry ClinicalTrials.gov lists no trial with Crystagen. A review by the developing research group reports on use in older people, but the original paper cannot be found in PubMed.

What is Crystagen?

The tripeptide Glu-Asp-Pro, EDP for short, from the Khavinson programme of tissue-specific bioregulators. An analysis of the thymus extract Thymalin found it, along with the dipeptide Lys-Glu (Vilon), as one of the active components.

What is known about effects in humans?

Only what the group's review reports: older people with weakened immunity received Crystagen by mouth on top of standard care. The immunogram normalised in 82 percent, in 56 percent without Crystagen. Mainly T cells rose and the effect on B cells was weaker. Fatigue eased in all. The number of participants is not given there.

What do cell and animal experiments show?

In irradiated rats the division of the thymus into cortex and medulla was preserved under Crystagen. EDP prompted mouse scavenger cells to produce the messengers IL-1, IL-6 and TNF-alpha and promoted the division of human thymic epithelial cells. In the ageing spleen Crystagen activated B cells without stimulating cell renewal.

Does Crystagen have anything to do with the skin?

In one paper the tripeptide Glu-Asp-Pro promoted cell division in skin cultures from young rats but not from old rats. Otherwise Crystagen is not classed for the skin, the programme lists it as a peptide for the immune system.

How is such a short peptide supposed to enter the cell?

That is unresolved. A computer analysis by the same group suggests transporters such as LAT1 and the peptide transporters of the POT family. For Crystagen it calculated a binding to LAT1 slightly stronger than that of the transporter's natural partners. This has not been measured.

Which side effects are known?

There are no solid data because Crystagen has never been tested in a registered human trial. The entry mainly lists local reactions at the injection site, independent safety data are missing.

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