TB-500 Co

TB-500 vs BPC-157

Every row cites its source. Where a cell reflects our own reading of the evidence rather than an external source, the row says so.

TB-500 vs BPC-157
AspectTb500Bpc157MirrorsCalibration NoteSource
What it isSynthetic 7-amino-acid fragment of thymosin beta-4; FDA lists it as Thymosin beta-4, fragment (LKKTETQ), also known as TB-500. 889 DaSynthetic 15-amino-acid fragment of the gastric juice protein BPC (GEPPPGKPADDAGLV). 1419.5 Darow1-source
Species of evidenceRat, mouse, horse and in vitro wound and tendon models for the fragment; FDA states it has not identified any human exposure data for the fragmentRodent and rabbit models across many organ systems; 2 in vitro lines; 1 uncontrolled human case series; 0 published human randomized trialsrow2-source
Head-to-head dataOne 2026 rat Achilles study (n=32, 8 per group): significant on maximum load to failure and on total Bonar (p=0.016) and Movin (p=0.017) scores versus control; combining both peptides added nothingSame study: numerically better histology than control, not statistically significant on total scoresrow3One exploratory rat study whose authors call the findings preliminary. It is not evidence of human benefit and we do not present it as a selling point. This is the same restraint the sister site applied when the result went the other way.source
Human trialsNone completed. One phase 1/2 safety study of the fragment is recruiting with no results posted. The full-length protein has 15 completed or terminated registered trials totalling 2,143 participants, but that is a different molecule3 small uncontrolled pilots (under 30 subjects); phase 2 hamstring RCT recruiting since 2026row4-source
FDA approvalNone; Drugs@FDA returns no productNone; Drugs@FDA returns no productrow5-source
FDA compounding positionOn the safety-risks list (immunogenicity from aggregation, peptide-related impurities, no human exposure data identified); July 2026 PCAC: FDA proposed NOT to include free base or acetate on the 503A listOn the same safety-risks list (immunogenicity, impurities); July 2026 PCAC: FDA proposed NOT to include free base or acetaterow6-source
WADA 2026 statusNamed under S2.3 (Thymosin-beta4 and its derivatives e.g. TB-500); prohibited at all times; S2 substances are non-Specified SubstancesNamed under S0 Non-Approved Substances; prohibited at all times; S0 substances are Specified Substancesrow7The distinction is real and runs against TB-500: Specified status is what can support an argument that a substance was taken for a reason other than performance. S2 does not carry it.source
Best-documented propertyActin binding: LKKTETQ is the actin-binding site of the parent protein, and the isolated 17-23 peptide reproduced anti-fibrotic activity in human cells. The marketed peptide itself is thinly characterised, and one rat study suggests a metabolite rather than the parent carries the wound-repair activityReported gastric-juice stability and activity by oral routes in rodent GI and ligament modelsrow8-source
What is in the vial (added row)A racing laboratory analysed marketed TB500 and TB1000 and reported content not systematically consistent with its descriptions; synthesis impurities are detectable in plasma after administration of TB4-containing productsReviewers flag unregulated manufacturing and contamination as adverse-effect pathways; no USP monograph or pharmaceutical-grade formulation existsnone (added by this site)-source
Documented large-animal use (added row)10 mg subcutaneously in thoroughbred horses, administered by racing laboratories to validate detection methods; TB-500 is explicitly named as a veterinary preparation in that literatureNo comparable equine administration literature; the animal record is dominated by rodent modelsnone (added by this site)-source

Researching TB-500 vs BPC-157 itself? Its dedicated guide site is at bpc157co.com.

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