Vesugen: research
An experimental blood-vessel peptide with unclear benefits and poorly defined safety.
Also called: Vezugen, KED, Lys-Glu-Asp, T-38.
Khavinson bioregulator peptides · Synthetic vascular tripeptide.
12 clinical papers and 2 patent examples found. Reports may include the same participants; these are not 14 independent trials.
Studies
- Truck drivers and stress. cohort, n=300, 150 male truck drivers and 150 male metal workers.. Combined Pinealon and Vesugen had the strongest reported changes in stress-related questionnaire scores. (source)
- Blood flow after leg-artery surgery. cohort, n=41, 41 patients after surgery for chronic lower-limb arterial insufficiency.. Authors reported better clinical and ultrasound measures after Vesugen. (source)
- Vascular report with conflicting indexing. cohort, n=41, 41 people; title describes leg disease, while the abstract describes vascular erectile dysfunction.. The abstract reports improved penile blood flow; the title and abstract do not match. (source)
- Older adults with several illnesses. cohort, n=32, Reported n=32, ages 41-83, with chronic illnesses and brain disorders in remission.. Aging-marker changes came with prooxidant activity and fewer circulating CD34+ cells. (source)
- Work-ability index report. cohort, Workers exposed to occupational hazards; sample size unavailable in the abstract.. Combined cytogens reportedly improved work-ability measures; Vesugen-specific effects cannot be isolated. (source)
- Comparison of aging interventions. cohort, n=110, 110 people in several age groups.. Vesugen plus Pinealon had the strongest reported changes in biological-age indicators. (source)
- Mouth inflammation after cancer therapy. cohort, n=22, 22 older adults after combined therapy for oropharyngeal cancer.. A regimen containing Vesugen and another supplement reportedly improved oral recovery. (source)
- Dry mouth after chemotherapy. cohort, n=27, 27 patients aged 61-75 after cancer chemotherapy, plus 13 healthy reference participants.. A multicomponent regimen improved saliva measures; it cannot establish Vesugen benefit alone. (source)
- Chronic salivary-gland inflammation. cohort, n=36, 36 adults aged 61-81 with a flare of chronic nonspecific salivary-gland inflammation.. Combination care reduced symptoms faster; the peptide contribution is unknown. (source)
- Dry mouth after radiation. cohort, Older patients with salivary-gland damage after oropharyngeal cancer therapy.. A regimen including Vesugen was reported to improve salivary function. (source)
- Salivary-gland disease in older adults. cohort, Hospitalized older adults with Mikulicz disease or Sjogren syndrome.. Exercise, massage and a multicomponent regimen including Vesugen reportedly improved symptoms. (source)
- Salivary disease, stress and sleep. cohort, n=69, 69 adults aged 61-85: cancer n=21, reactive disease n=16, drug/radiation injury n=32.. Adding an anxiety medicine, rather than Vesugen alone, was linked to better stress and sleep measures. (source)
- Patent only: capillary fragility. case-series, Adults aged 19-35 with signs of vitamin deficiency.. The patent claims fewer petechiae after injections; enrollment counts conflict. (source)
- Patent only: age-related purpura. case-series, n=23, 23 adults aged 70-82 with age-related purpura.. The patent claims improved capillary and clotting measures. (source)
- Identity and cell differentiation. in-vitro, Aging human cell cultures.. Vesugen was identified as Lys-Glu-Asp and changed differentiation markers in fibroblasts. (source)
- Vascular cells and Ki-67. in-vitro, Cultured vascular cells from young and old animals; computer docking.. Vesugen increased Ki-67; docking proposed an interaction near its gene promoter. (source)
- Vascular cell renewal. in-vitro, Organ and dissociated vascular cell cultures.. T-38 increased Ki-67 and reduced p53 and E-selectin expression. (source)
- Atherosclerosis and restenosis models. in-vitro, Cultured vascular endothelium under disease-model conditions.. KED changed endothelin-1, connexins and SIRT1 expression in cells. (source)
- Stem-cell aging signals. in-vitro, Human embryonic bone-marrow stem cells aged in culture.. Short peptides including KED altered IGF1, FOXO1 and other aging-related genes. (source)
- Neurons made from donor skin cells. in-vitro, Induced neurons made from older human donors' fibroblasts.. KED promoted dendrite branching; it did not improve mitochondrial, lysosomal or p16 measures. (source)
- Cyclophosphamide and spleen tissue. in-vitro, Rat spleen tissue explants exposed to cyclophosphamide.. T-38 reduced the growth-suppressing effect of cyclophosphamide in cultured tissue. (source)
- Short peptides under low oxygen. animal, Animal low-oxygen models.. Several peptides showed activity; Pinealon had the strongest reported effect. (source)
- KED in an Alzheimer mouse model. animal, 5xFAD-M mice and control mice.. KED changed spine shape; total spine density did not significantly change. (source)
Vesugen dosage
Typical reported dose: 1 mg once a day
- One capsule twice daily: 1 capsule twice daily with food; peptide mass unstated. twice daily, by mouth. Studied in a trial. Studied in: Adults aged 61-75 with salivary injury after chemotherapy. (source)
- One-month salivary-gland regimen: 1 capsule twice daily; peptide mass unstated. twice daily, by mouth. Studied in a trial. Studied in: Adults aged 61-81 with chronic salivary-gland inflammation. (source)
- Discharge advice: two courses yearly: 1 capsule orally twice daily with food for 30 days; peptide mass unstated. twice daily, by mouth. Clinician-published. Studied in: Older adults in the combination-care group after hospital discharge. (source)
- One tablet three times daily: 1 tablet three times daily; peptide mass unstated. three times daily, by mouth. Studied in a trial. Studied in: 69 adults aged 61-85 with chronic salivary-gland disease. (source)
- One milligram daily report: 1 mg once daily. once daily, under the skin. Reported by users, rare report. Studied in: Adults in online discussions; frequency in the wider community is unknown. (source)
These are doses reported in labels, trials or user reports, not a personal plan. Check the source behind each one.
Vesugen side effects and risks
Reported side effects
- Allergic or injection-related reactions: No compound specific rate is established. These are general risks of unapproved peptide products., serious. Stop use and seek care for a spreading reaction or signs of infection. (source)
- Other short- and long-term effects: No reliable adverse event denominator is available., moderate. Report new symptoms and the exact product, dose, route and timing. (source)
- Prooxidant and blood-cell-marker changes: One 32 person report noted increased oxidation signals and lower circulating CD34+ cells; no rates or clinical harms were quantified., moderate. Discuss unexplained bruising, infection or fatigue and whether a blood count is needed. (source)
Stop and get help if
- Trouble breathing, throat swelling, widespread hives or collapse: Call emergency services now; these may be signs of anaphylaxis.
- Fever with confusion, rapid breathing or a very painful spreading injection-site infection: Get emergency care now; severe infection can progress quickly.
- Sudden face droop, one-sided weakness, speech trouble or vision loss: Call emergency services now, even if symptoms improve. These can be stroke signs.
- Chest pressure or pain with shortness of breath, sweating or lightheadedness: Call emergency services now for possible heart attack.
Who should avoid it
- pregnant: Precaution: no reliable pregnancy safety data for this peptide.
- breastfeeding: Precaution: transfer into milk and infant effects are unknown.
- tryingToConceive: Precaution: fertility and early-pregnancy effects are unknown.
- under18: Precaution: no reliable pediatric safety evidence was located.
- kidneyDisease: Clearance and dose adjustment in kidney disease are unknown.
- liverDisease: No liver-disease dose or safety study was located.
- testedAthlete: The 2026 S0 rule is expected to prohibit this unapproved substance at all times.
- activeCancer: Precaution: KED alters cell-growth and IGF1 signals in culture. Effects on tumor growth in people are unknown.
- cancerHistory: Small post-cancer dental reports do not establish recurrence safety.
- bleedingDisorder: Patent claims include changes in clotting tests; effects on bleeding and thrombosis are unconfirmed.
- heartCondition: Small vascular reports do not show protection from heart attack or stroke.
Interactions
- Anticoagulants and antiplatelet drugs: Interaction unstudied. Patent clotting-test changes make combined use a precaution, not a proven interaction.
- Cyclophosphamide: KED reduced cyclophosphamide growth suppression in rat tissue culture. Whether this affects cancer therapy is unknown.
- Other experimental bioregulators and recovery peptides: Small reports and forum stacks cannot establish interaction safety or attribute effects to one peptide.
Product quality risks
- No independent published market-testing study specific to this peptide was located.
- General peptide warnings describe wrong strength, wrong ingredients and microbial contamination.
- An online semaglutide study found low purity and endotoxin. This does not measure contamination in this peptide.
How Vesugen works
In cell studies, it changes signals linked to growth and aging in blood-vessel lining cells. Some researchers propose that it affects which genes are active. No specific receptor or proven mechanism in people has been established.
- Ki-67 and p53: Cell experiments found more growth-marker expression and less p53 expression.
- Endothelin-1, connexins and SIRT1: Expression changed in cultured vessel cells; this does not prove improved circulation in people.
Half-life: Unknown in humans.
Gaps: No registered human trial, reliable pharmacokinetic study or dose-finding program was found. No human subcutaneous or intranasal studied maximum is known; oral and patent IM amounts cannot supply one. Human reports often omit doses, arm counts, adverse-event rates or numerical outcomes. Several cohorts may overlap. The 2014 vascular record has a title/abstract mismatch. An inaccessible 2016 conference report mentions 59 patients; overlap and full methods need checking. A 2005-2006 developer report is distributed through sellers; independent primary verification was not obtained. Long-term cancer, reproductive, immune and organ safety remain unknown. No verified microdosing ladder or validated storage instructions were found.
Related to Vesugen
- Epitalon: A peptide with telomerase effects in cells, but no proof that people live longer.
- Pinealon: A peptide with unproven brain benefits and no established injection dose.
- Thymalin: A calf thymus extract studied for immune problems, with uncertain safety and product identity.
- Thymogen: A Russian peptide used for immune problems, with negative cancer trials.
- Cortagen: A four-amino-acid brain peptide backed mainly by animal work and unverified patent claims.
- BPC-157: An experimental repair peptide with mostly animal evidence and a few small human reports.
Sources
- 21 CFR 216.23 — Bulk drug substances that can be used to compound drug products in accordance with section 503A of the Federal Food, Drug, and Cosmetic Act., Office of the Federal Register · eCFR · 2026
- 503B Bulk Drug Substances List, FDA · FDA · 2026
- Bulk Drug Substances Nominated for Use in Compounding Under Section 503A of the Federal Food, Drug, and Cosmetic Act, US Food and Drug Administration · 2026
- Bulk Drug Substances Used in Compounding Under Section 503A of the FD&C Act, FDA · FDA · 2026
- Find product information about medicines, Medicines and Healthcare products Regulatory Agency · MHRA · 2026
- Medicines, European Medicines Agency · European Medicines Agency · 2026
- The Prohibited List, World Anti-Doping Agency · World Anti-Doping Agency · 2026
- Think twice before injecting peptides bought online: unauthorized products can seriously harm you, Health Canada · Health Canada · 2026
- Understanding your responsibilities when importing, compounding and supplying unapproved peptide products, Therapeutic Goods Administration · Therapeutic Goods Administration · 2026
- Bulk Drug Substances Nominated for Use in Compounding Under Section 503B of the Federal Food, Drug, and Cosmetic Act, FDA · FDA · 2025
- Anaphylaxis, National Library of Medicine
- Drugs@FDA: FDA-Approved Drugs, US Food and Drug Administration
- Heart Attack, National Library of Medicine
- Sepsis, National Library of Medicine
- Stroke, National Library of Medicine
Sources checked: 2026-10-18.
Information only, not medical advice. Peptifacts does not sell anything and does not link to sellers.