Short answer: BPC-157 has a little human evidence and TB-500 has none. They are different peptides: BPC-157 is a 15-amino-acid chain based on a stomach protein; TB-500 is a 7-amino-acid fragment of thymosin beta-4, the piece that binds the cell protein actin. Both are sold for injury recovery on the strength of animal and lab studies. The FDA found five small human reports for BPC-157 and no human data at all for TB-500. Neither is approved, both are banned in sport, and the popular blend of the two has never been tested.
BPC-157 vs TB-500 at a glance
| BPC-157 | TB-500 | |
|---|---|---|
| What it is | Synthetic gastric pentadecapeptide (15-amino-acid peptide) | Synthetic thymosin beta-4 fragment (actin-binding peptide) |
| Approval | Not approved; furthest stage: Phase 2 (one ulcerative colitis trial, reported only as a 2005 meeting abstract) | Not approved; furthest stage: Preclinical (no completed human study of TB-500) |
| Human studies (counted in our records) | 5 | 0 |
| Half-life | Not established in humans | Not established in humans |
| Testosterone suppression score | Not established | Not established |
| Liver risk score | Not established | Not established |
| Evidence score | 0/3 | 0/3 |
| WADA | Prohibited at all times (S0 Non-approved substances) | Prohibited at all times (S2.3 Growth factors and growth factor modulators) |
| Size | 15 amino acids | 7 amino acids (Ac-LKKTETQ) |
| FDA panel vote, 23 July 2026 | 8–6 for compounding (ulcerative colitis) | 8–6 for compounding (wound healing) |
| SwissChems product | BPC-157 (0.5mg/capsule), 60 Capsules | TB-500 (Thymosin Beta-4) |
Scores run from 0 (none) to 3 (high); see our methodology. Data from the SARMs database.
Source: Sarmguide compound database; BPC-157: FDA Briefing Document, Pharmacy Compounding Advisory Committee, 23-24 July 2026: BPC-157-related bulk drug substances (2026).
How they work
BPC-157 is a synthetic 15-amino-acid peptide (Gly-Glu-Pro-Pro-Pro-Gly-Lys-Pro-Ala-Asp-Asp-Ala-Gly-Leu-Val) derived from a protein in gastric juice. In animal and lab studies it sped up healing of tendons and gut and increased blood-vessel growth with raised VEGFR2 signaling, but the FDA notes its molecular target is still unknown.
TB-500 is the acetylated fragment 17–23 of thymosin beta-4 (Ac-LKKTETQ), the part of the protein that binds actin. “TB-500” is a trade name, and the FDA has seen different salts and molecules sold under it; products are often labeled “thymosin beta-4”, which is actually the full 43-amino-acid protein. In lab tests, a breakdown product of TB-500 (Ac-LKKTE), not TB-500 itself, sped up wound closure in fibroblasts; the FDA found no studies showing TB-500 itself promotes wound healing.
What the human evidence shows
| BPC-157 | TB-500 | |
|---|---|---|
| Human studies | 5 small reports: UC enema trial (53 people, abstract only), Phase 1 enema study (32), knee-pain chart review (16), bladder-pain pilot (12), IV safety pilot (2) | None completed; a Phase 1/2 trial (NCT07487363) was registered in 2026 |
| Quality | A 2026 systematic review rated the certainty very low | No human data |
| Related molecule data | None | Full-length thymosin beta-4 (a different molecule) was tested as eye drops and IV infusions; those results do not transfer to TB-500 |
| Half-life | Not measured in people; under 30 min IV in rats and dogs | Not measured in people |
Side effects
For BPC-157, the enema studies reported headache and flatulence at placebo-like rates, and the FDA’s adverse event database holds three reports (injection-site swelling, shortness of breath, and skin and gum darkening). For TB-500, the FDA found no clinical studies and no adverse event reports. The one skin-darkening report involved a “research use” product containing both peptides, so which one caused it is unclear. For both, the FDA warns that injected peptides can aggregate or carry impurities that trigger immune reactions, and for TB-500 that buyers may not get the molecule on the label.
Regulatory status
Neither is an approved drug. Both were nominated for US pharmacy compounding and then withdrawn from the FDA’s Category 2 safety-risk list. At the FDA Pharmacy Compounding Advisory Committee on 23 July 2026, members voted 8–6 (1 abstention) to recommend adding BPC-157 for ulcerative colitis and, separately, 8–6 (1 abstention) for TB-500 for wound healing, after FDA staff advised against both. The vote is non-binding; the FDA had not made a final decision as of 30 October 2026. In Australia both are Schedule 4 prescription-only medicines. See our news post on the FDA panel vote.
In sport
WADA bans both at all times, in different sections: BPC-157 under S0 (non-approved substances) and TB-500 under S2.3 (thymosin beta-4 and its derivatives). Anti-doping labs have validated urine tests for BPC-157 and include TB-500 in peptide screening.
BPC-157 and TB-500 together
The blend is popular because the two are thought to work through different routes (blood-vessel growth vs actin binding). No study has tested the combination, and the only human report involving both is the FDA’s skin-darkening case. SwissChems sells each separately and as a BPC-157 + TB-500 blend.
Verdict
If the question is which has more evidence, BPC-157, but “more” means five small reports of very low certainty. TB-500 has no human data, and the strongest results attributed to it come from studies of the full thymosin beta-4 protein, a different molecule. Both are unapproved, banned in sport, and only narrowly backed by an FDA panel for specific medical uses. Read the full BPC-157 review and TB-500 review, and see peptides for healing and recovery.
Frequently asked questions
What is the difference between BPC-157 and TB-500?
Different peptidesEvidence: Lab
BPC-157 is a 15-amino-acid peptide based on a stomach protein; TB-500 is a 7-amino-acid fragment of thymosin beta-4 (Ac-LKKTETQ). They act differently and have different evidence.
Is BPC-157 or TB-500 better?
Neither is provenEvidence: Limited
BPC-157 has more evidence, but only five small human reports rated very low certainty. TB-500 has no completed human study.
Can you take BPC-157 and TB-500 together?
Combination never studiedEvidence: Limited
No study has tested the combination. The only human report involving both is an FDA case of skin and gum darkening with a blend.
Is TB-500 the same as thymosin beta-4?
NoEvidence: Lab
TB-500 is a 7-amino-acid fragment; thymosin beta-4 is the full 43-amino-acid protein. Results from thymosin beta-4 trials do not apply to TB-500.
Are BPC-157 and TB-500 FDA approved?
NoEvidence: Law
In July 2026 an FDA advisory panel voted 8–6 to back compounding of each for specific uses. The vote is non-binding and the FDA had not decided as of 30 October 2026.
What are the side effects of TB-500?
Unknown in humansEvidence: Limited
The FDA found no clinical studies and no adverse event reports. It warns about immune reactions and products that may not contain the labeled molecule.
Are BPC-157 and TB-500 banned in sport?
Yes, banned by WADAEvidence: Law
WADA bans BPC-157 under S0 and TB-500 under S2.3, at all times.
Sources
- FDA Briefing Document, Pharmacy Compounding Advisory Committee, 23-24 July 2026: BPC-157-related bulk drug substances
- FDA Briefing Document, Pharmacy Compounding Advisory Committee, 23-24 July 2026: TB-500-related bulk drug substances
- Human evidence for BPC-157 in orthopaedic and regenerative medicine: a systematic review of efficacy and safety
- Pharmacokinetics, distribution, metabolism, and excretion of body-protective compound 157, a potential drug for treating various wounds, in rats and dogs
- Intra-Articular Injection of BPC 157 for Multiple Types of Knee Pain
- Effect of BPC-157 on Symptoms in Patients with Interstitial Cystitis: A Pilot Study
- Safety of Intravenous Infusion of BPC157 in Humans: A Pilot Study
- Therapeutic potential of pro-angiogenic BPC157 is associated with VEGFR2 activation and up-regulation
- Simultaneous quantification of TB-500 and its metabolites in in-vitro experiments and rats by UHPLC-Q-Exactive orbitrap MS/MS and their screening by wound healing activities in-vitro
- 0.1% RGN-259 (Thymosin ß4) Ophthalmic Solution Promotes Healing and Improves Comfort in Neurotrophic Keratopathy Patients in a Randomized, Placebo-Controlled, Double-Masked Phase III Clinical Trial
- A randomized, placebo-controlled, single and multiple dose study of intravenous thymosin beta4 in healthy volunteers
- ClinicalTrials.gov NCT07487363: Phase 1/2 study of TB-500 (thymosin beta 4 17-23 fragment) in stable atherosclerotic cardiovascular disease (recruiting)
- AJMC: FDA Panel Backs 6 Peptides for Compounding (31 Jul 2026)
- World Anti-Doping Code International Standard: Prohibited List 2026
- PubChem: BPC 157 (CID 9941957), sequence Gly-Glu-Pro-Pro-Pro-Gly-Lys-Pro-Ala-Asp-Asp-Ala-Gly-Leu-Val, C62H98N16O22