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BPC-157

Evidence grade: Animal studies only

A gastric-juice-derived peptide with an unusually broad animal literature on tissue repair — and a persistent absence of human trials.

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TB-500

Evidence grade: Animal studies only

A synthetic fragment of thymosin beta-4, studied for cell migration and tissue repair — frequently paired with BPC-157 in repair protocols.

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2 cited sourcesNo human data on fileReviewed 1 Jun 2026
1 cited sourceNo human data on fileReviewed 1 Jun 2026

At a glance

At a glance compared across BPC-157, TB-500
AttributeBPC-157TB-500
Primary useNerve & tissue repairNerve & tissue repair
Evidence gradeAnimal studies onlyAnimal studies only
Human dataNo human citations on fileNo human citations on file
Cited sourcesdiffers2 sources · 0 human1 source · 0 human
In one sentenceA gastric-juice-derived peptide with an unusually broad animal literature on tissue repair — and a persistent absence of human trials.A synthetic fragment of thymosin beta-4, studied for cell migration and tissue repair — frequently paired with BPC-157 in repair protocols.

Mechanism

Mechanism compared across BPC-157, TB-500
AttributeBPC-157TB-500
How it is thought to workBPC-157 is a synthetic fragment of a protein found in human gastric juice. In animal models it accelerates healing across tendon, muscle, gut and nerve tissue, apparently by upregulating VEGF and promoting angiogenesis, and by interacting with the nitric oxide system. A substantial body of rodent work also reports effects on the gut-brain axis and on dopaminergic systems.Thymosin beta-4 is the primary actin-sequestering protein in cells and governs cell migration. TB-500 reproduces its active region. Because repair requires cells to travel to the injury site, promoting migration accelerates several stages of healing simultaneously — alongside reported angiogenic and anti-inflammatory effects.
What the research reports
  • Accelerated tendon, ligament and muscle healing in rodents
  • Protection and healing of gut mucosa, including NSAID-induced damage
  • Peripheral nerve regeneration after crush injury in rats
  • Counteraction of dopamine-system disturbances in rodent models
  • Accelerated wound healing and reduced scarring in animal models
  • Cardiac repair after infarction in rodents
  • Corneal and dermal healing studies
  • Neuroprotection and improved functional recovery after TBI in rats
What it is NOT shown to do
  • No published randomised controlled trial in humans
  • Banned by WADA for competitive athletes
  • The gut-brain and dopamine findings are entirely rodent-based
  • No human efficacy trials for musculoskeletal repair
  • Banned by WADA
  • No mental-health data of any kind

Dosing & pharmacology

Dosing & pharmacology compared across BPC-157, TB-500
AttributeBPC-157TB-500
Routes studieddiffersSubcutaneous, OralSubcutaneous, Intramuscular
Half-lifediffersShort in plasma; reported to be unusually stable in gastric juiceLonger-acting than BPC-157, which is why twice-weekly dosing is conventional
Dose referenceCommonly cited research amounts are 200–500 mcg/day, often subcutaneously near the injury site. This is community convention, not a trial-derived dose.Community protocols commonly cite 2–5 mg twice weekly during a loading phase. Not trial-derived.
Typical study cyclediffersCommunity protocols run 4–8 weeks, then a breakLoading phase of 4–6 weeks, then reduced frequency

Chemistry & handling

Chemistry & handling compared across BPC-157, TB-500
AttributeBPC-157TB-500
SequenceGly-Glu-Pro-Pro-Pro-Gly-Lys-Pro-Ala-Asp-Asp-Ala-Gly-Leu-Val (GEPPPGKPADDAGLV)Ac-Leu-Lys-Lys-Thr-Glu-Thr-Gln (Ac-LKKTETQ), the active fragment of thymosin β4
Molecular formuladiffersC62H98N16O22C31H56N8O11
Molecular weightdiffers1419.5 g/mol716.8 g/mol
CAS numberdiffers137525-51-0885340-08-9 (fragment) · 77591-33-4 (full thymosin β4)
Storage (reconstituted)2–8 °C, typically used within 2–4 weeks2–8 °C, typically used within 2–4 weeks

Risk

Risk compared across BPC-157, TB-500
AttributeBPC-157TB-500
Reported side effects
  • Injection-site reaction
  • Nausea in some users
  • Reported as well tolerated in animals, but human data is anecdotal
  • Injection-site reaction
  • Lethargy reported anecdotally
  • Head-rush sensations
Contraindications
  • Active or historic cancer — the angiogenic mechanism is a genuine theoretical concern
  • Pregnancy and breastfeeding
  • Competitive athletes under WADA testing
  • Active or historic cancer — cell migration promotion is a theoretical metastasis concern
  • Pregnancy and breastfeeding
  • WADA-tested athletes