Ovagen for Health & Longevity - Quick Reference Sheet

Ovagen for Health & Longevity

Created on 09/22/2026 – Quick Reference based on Evidence Review created using AI4L / Opus 5 – Audit

Ovagen is a three-amino-acid compound from a Russian family of very short amino acid products, sold for liver and digestive support. No study has given Ovagen to a person; its results in the international literature are in cells and animals, and both were kidney rather than liver. Every listed benefit sits at the lowest level of confidence. The documented risks attach to how the product is obtained, not the compound. (Full Review)

Protocol

Standard oral course
1–2 × 10 mg capsules twice daily
Before food, 10–20 consecutive days, repeated 2–3 times per year
Injectable alternative
100–150 mcg daily, subcutaneous
10–20 days, reconstituted from freeze-dried powder
Best time of day
Morning, empty stomach
20–30 minutes before the first meal, so dietary peptides do not compete for the same intestinal carrier
Time to effect
Time to effect
Nothing establishes one
No study has measured any endpoint on any timescale
Course-based, not lifelong
10–20 day course
Nothing supports indefinite dosing; no long-term exposure data exist
Cycling for efficacy
2–3 courses per year
3–6 month gaps; the stated rationale is unmeasured

Benefits

Contraindications
  • Active malignancy, or in remission less than 5 years
  • Solid-organ transplant recipients on maintenance immunosuppression
  • Immunosuppressants and cytotoxic chemotherapy (tacrolimus, ciclosporin, methotrexate) during active treatment
  • Pregnancy, lactation, and anyone under 18 years
  • Decompensated cirrhosis (Child-Pugh Class C) or acute hepatitis with alanine aminotransferase above 5 times the upper limit of normal
  • Advanced chronic kidney disease (estimated glomerular filtration rate below 30 mL/min/1.73 m²)
  • Known hypersensitivity to the preparation or its excipients
Key Interactions
  • Beta-lactam antibiotics and other PEPT1 substrates (cefadroxil, cephalexin, valacyclovir, enalapril)
  • Acid-suppressing medicines (omeprazole, esomeprazole, famotidine, calcium carbonate antacids)
  • Dietary protein and peptide-rich meals
  • Hepatotoxic agents (paracetamol above 3 g/day, high-dose niacin, kava, green tea catechin extracts)
  • Supplements acting on the same liver targets (silymarin, N-acetylcysteine, tauroursodeoxycholic acid)
  • Other organ bioregulator peptides (Epitalon, Pinealon, Livagen)

Risk & Side Effects

  • Low: Contaminated or Misidentified Product; Injection-Site Infection and Injury
  • Speculative: Suppression of Cell-Cycle Brakes; Hypersensitivity and Immune Reaction; Delayed Evaluation of Abnormal Liver Tests

Monitoring

Marker Target Why
Alanine aminotransferase (ALT) 10–26 U/L (men), 8–22 U/L (women) Most liver-specific enzyme; the primary response marker
Aspartate aminotransferase (AST) 10–26 U/L Pairs with ALT; a ratio above 1 points to alcohol or fibrosis
Gamma-glutamyl transferase (GGT) Below 25 U/L (men), below 18 U/L (women) Sensitive to alcohol, bile flow and oxidative load
Alkaline phosphatase (ALP) 60–90 U/L Detects bile obstruction, the main alternative explanation for liver symptoms
Total bilirubin 0.4–1.0 mg/dL Bile handling and red cell turnover
Albumin 4.2–5.0 g/dL Synthetic liver function; falls only with genuine impairment
Platelet count 200–350 ×10⁹/L A falling count is the earliest routine sign of portal hypertension
Fibrosis-4 index (FIB-4) Below 1.30 Calculated fibrosis screen; decides whether imaging is warranted
High-sensitivity C-reactive protein (hs-CRP) Below 1.0 mg/L Background inflammation that confounds liver enzyme readings
Estimated glomerular filtration rate (eGFR) Above 90 mL/min/1.73 m² Ovagen's only published cell data are renal, and its clearance is unstudied
Liver stiffness by transient elastography Below 6.0 kPa Direct fibrosis measure; the hard endpoint any liver claim must move
Ovagen-specific response marker No established target exists; track the change from the individual's own pre-course values across the panel above No validated biomarker of Ovagen activity has been defined

Cadence: Baseline before the first course; liver panel at the end of each 10–20 day course, again 4 weeks later, then every 6–12 months while courses continue. Kidney function and elastography repeat annually; any value moving the wrong way is rechecked at 2 weeks.

Qualitative Assessment

  • Digestive comfort: bloating, fullness, stool regularity
  • Energy and clarity: morning energy, afternoon slump, rated 1 to 10
  • Sleep: total time and awakenings
  • Skin and appetite: itching, yellowing or appetite loss, all warning signs