Crystagen
Khavinson bioregulator peptide
Also known as: Crystagen peptide, immune bioregulator, Khavinson immune peptide
Evidence level: Early/animal research
What it is
Crystagen is a short synthetic peptide from the Russian 'Khavinson' bioregulator family, marketed for the immune system. In a lab study of aging spleen cells, it activated B-cells, the immune cells that make antibodies, though unlike some peptides tested it didn't drive new cell growth as the spleen aged. The research is Russian-led, preclinical, hasn't been independently replicated in the West, there are no human trials, and Crystagen isn't FDA-approved.
What the research found
Crystagen is marketed as an immune-system "bioregulator." In a lab study of aging spleen cells, it activated B-cells (antibody-producing immune cells), though — unlike some peptides tested — it did not drive cell renewal as the spleen aged. This fits a broad tissue-specific peptide theory but is a laboratory finding; there are no large controlled human trials showing Crystagen treats any condition.
Status and regulatory position
Not a drug in the US and not FDA-approved for any indication. A synthetic "Khavinson" short-peptide bioregulator ("cytogen") from the St. Petersburg Institute of Bioregulation and Gerontology (Russia), associated with the immune system. Evidence is almost entirely preclinical (cell) plus small Russian studies; no large controlled human trials. WADA: not specifically named; best treated as S0 (non-approved), prohibited at all times — verify with your anti-doping organization. Not DEA-scheduled.
Safety
Crystagen has essentially no controlled human safety data and is not FDA-approved. It is not a treatment for any immune condition. As a non-approved research peptide it is best treated as prohibited in regulated sport (WADA S0). VialWise is a research and educational reference, not medical advice.
Disclosures
⚠️ For research and educational purposes only. Crystagen is not FDA-approved and is not a treatment for any immune or other condition. Its evidence is preclinical. Information here is informational, not medical advice.
⚠️ Part of the Khavinson "bioregulator" family — read the shared caveat. Crystagen is one of a set of short peptides from the St. Petersburg Institute of Bioregulation and Gerontology, sharing a thin, mostly-preclinical, largely single-institute evidence base and no large controlled human trials.[²]
Quick reference
| Compound class | Synthetic short peptide; a "Khavinson" cytogen associated with the immune system.[¹] |
|---|---|
| Common vial sizes | Research-supply lyophilized vials, commonly ~; also an oral capsule supplement in Russia. No FDA-approved product. |
| Frequency | Short courses (~10 days) in Russian practice; not validated. |
| Half-life | Not established; expected to clear quickly. |
| Route | Intramuscular/subcutaneous (injectable) or oral capsule. No approved route. |
| Onset of action | No validated clinical effect or timeline. |
In depth
Crystagen is a synthetic short peptide in the "Khavinson" bioregulator family, associated with the immune system. According to PubMed, a study of Khavinson peptides in aging spleen reported that Crystagen activated B-cells (the immune cells that produce antibodies); notably, unlike some other peptides tested, Crystagen did not cause cell renewal in the aging spleen.[¹] This underpins its marketing as an immune peptide under the Khavinson tissue-specific theory.[²]
Evidence quality. Preclinical (cell). No large controlled human trials. See the shared Khavinson caveat below.
### About the Khavinson bioregulators (shared framing)
Developed from the 1970s by Vladimir Khavinson at the St. Petersburg Institute of Bioregulation and Gerontology, these cytomedin/cytogen peptides went from organ-extract complexes to synthetic short peptides proposed to have tissue-specific effects under a "peptide theory of ageing."[²] Honest caveats: evidence is overwhelmingly preclinical plus small, often non-blinded Russian studies; no large independent randomized trials; none FDA-approved; sold in Russia as injectables and supplements.
Regulatory status (US). Not FDA-approved; not a drug. Not DEA-scheduled.
Regulatory status (sport — WADA). Not specifically named; best treated as S0 (non-approved), prohibited at all times. Verify with your anti-doping organization.
Common research interests. Immune support (its associated system). Extrapolated from preclinical data, not an established human use.
Reported side effects
Commonly reported
- Injection-site reactions
- Reactions to research-supply material of variable purity
- Immune modulation. Crystagen activates B-cells in vitro;[¹] consequences of modulating immunity in humans are uncharacterized.
- Unknown long-term safety.
Contraindications and warnings
Not a treatment for any immune condition — see a clinician
Autoimmune disease / immunosuppression — caution given the immune-modulating signal
Pregnancy and lactation — no data; default to contraindicated
Pediatric use — no data; not for researchers under 18
Known hypersensitivity — contraindicated
Regulatory note (US): Not FDA-approved; not DEA-scheduled.
Regulatory note (sport): Best treated as WADA S0. Verify with your anti-doping organization.
Key terms
- Bioregulator (Khavinson peptide)
- A very short synthetic peptide from the St. Petersburg Institute of Bioregulation and Gerontology, each linked to a tissue — here, the immune system.
- B-cell
- An immune cell that makes antibodies. Crystagen activated these in the lab.
- Spleen
- An immune organ; the tissue used in the Crystagen study.
- Preclinical
- Research in cells or animals, before human testing.
Sources
- Chervyakova NA, Linkova NS, Chalisova NI, Koncevaya EA, Trofimova SV, Khavinson VKh. (2014). [Molecular aspects of immunoprotective activity of peptides in spleen during the ageing process]. Advances in Gerontology (Uspekhi Gerontologii), 27(1):224–228.(PMID 28976144)
- Khavinson VKh. (2002). Peptides and Ageing. Neuro Endocrinology Letters, 23 Suppl 3:11–144.(PMID 12374906)
Related entries
Entry last updated 2026-09-03. Sourced from published literature and regulatory labelling; see Sources above.