TB-500

Reviewed

Short answer

A seven-amino-acid piece of thymosin beta-4 promoted for repair, without reliable human healing evidence and with major product and anti-doping limits. No FDA-approved TB-500 drug product.

The Peptide Field explains research. Its pages are not independently medically reviewed, and they do not diagnose, prescribe, or recommend treatment.

Read the study findings

Also known as TB500 · Ac-LKKTETQ · thymosin beta-4 fragment 17-23

Part of Healing and recovery peptides

Compared with BPC-157

Sold in blends Wolverine · GLOW · KLOW

Legal status Is TB-500 legal? See the status table

Study and product details

What it is

TB-500 is reported as a seven-amino-acid piece, or fragment, of thymosin beta-4. It is not full-length thymosin beta-4, and evidence about the full protein cannot automatically be transferred to the fragment.

Type of peptide: Synthetic thymosin beta-4 fragment. This describes what the substance is or how it works. It does not show that it is safe, effective, or approved.

What has been studied?

  • Unclear: There is not enough reliable detail about the product or research to judge.
  • Limited: Research is too small or incomplete, or does not directly answer this question.
Did people's health improve?
Unclear

FDA found no adequate human clinical outcome evidence for compounded TB-500 wound-healing use.

What body changes did studies in people measure?
Limited

Fragment identity and laboratory findings do not establish a clinical benefit in people.

What do we know about risks in people?
Unclear

Human exposure and product-specific safety information are inadequate.

Do we know what the product contains and how well it was made?
Unclear

Nomenclature, salt form, purity, sterility, and fragment-versus-protein distinctions create major uncertainty.

Products with the same ingredient can differ.

The ingredient name does not tell you everything about a product. Check its other ingredients, its form, how it enters the body, and the use and people covered by the research or approval.

Approved products

None identified in the United States.

Approved or reviewed uses
  • No FDA-approved indication

Have a lab test report (COA) for a product sold under this name? Check what the report shows in 10 questions

Not sure if a product sold under this name is a prescription, compounded, or research-only vial? Sort it in 5 questions

What studies found

Findings

FDA has published a detailed 2026 briefing on TB-500's identity, characterization, proposed wound-healing use, and evidence gaps. WADA explicitly names TB-500 on the 2026 Prohibited List.

What remains unknown

Reliable controlled studies in people do not establish faster tendon, muscle, or wound healing from TB-500. Safety, purity, sterility, long-term effects, and equivalence of marketed material remain uncertain.

Which products do these findings apply to?

TB-500 is not the same as the full thymosin beta-4 molecule. FDA identifies TB-500 as a seven-amino-acid fragment, not as interchangeable with full-length thymosin beta-4. Internet naming and certificates do not establish product identity or clinical equivalence.

TB-500 side effects and safety: what FDA has said

This page has no trial or drug-label side-effect table for TB-500. FDA keeps a page of bulk substances that may be risky when a pharmacy mixes (compounds) them. Here is what that page says about TB-500, in plain words.

FDA's page does not name specific side effects for TB-500.

  • FDA found no data on people who received TB-500 products.
  • FDA says it lacks important safety information, including whether it would harm people.
  • The body's immune system may react against it. FDA says this risk depends on how it is given.
  • The peptide may clump together, which adds to that risk.
  • Making it may leave unwanted peptide by-products in the product.

These points come from FDA's review of compounded drugs. They are not a full list of side effects. Having no reports does not mean a product is safe.

Read FDA's exact words

Thymosin beta-4, fragment (LKKTETQ), also known as TB-500: “Compounded drugs containing thymosin Beta-4, Fragment (LKKTETQ) may pose risk for immunogenicity for certain routes of administration due to the potential for aggregation as well as peptide-related impurities. FDA has not identified any human exposure data drug products containing Thymosin Beta-4, Fragment. FDA lacks important information regarding any safety issues raised by this drug, including whether it would cause harm if administered to humans.”

Source: FDA, Certain bulk drug substances for use in compounding that may present significant safety risks , page dated .

Compare side-effect data across peptides

Report a side effect

You can report a suspected side effect to the FDA at 1-800-FDA-1088 or through FDA MedWatch . If a reaction feels serious, get medical care first.

FDA page checked .

Fact checks

3 statements checked. Read what the results mean.

Body changes and lab tests

“TB-500 is the same thing as thymosin beta-4.”

Misleading

FDA describes TB-500 as a seven-amino-acid fragment of the much larger thymosin beta-4 molecule.

What this answer is based on
Official record or product label
Limits of this answer
Chemical identity, not a claim about all possible biological activity.
Sources for this fact check (1)
Read the full answer ↗
Performance and recovery

“TB-500 accelerates tendon and muscle healing in people.”

Not established

The FDA evidence review did not identify adequate human outcome evidence for wound-healing use.

What this answer is based on
No reliable studies showing this health result in people
Limits of this answer
Clinical tendon, muscle, and wound-healing outcomes in people.
Sources for this fact check (1)
Read the full answer ↗
Performance and recovery

“TB-500 is allowed in tested sport.”

Misleading

TB-500 is named on the current WADA Prohibited List.

What this answer is based on
Official record or product label
Limits of this answer
Sport governed by the World Anti-Doping Code.
Sources for this fact check (1)
Read the full answer ↗

Questions people ask about TB-500

What has FDA said about TB-500 safety?

FDA's page on risky compounding substances says this about TB-500. It does not name specific side effects for TB-500. FDA found no data on people who received TB-500 products. FDA says it lacks important safety information, including whether it would harm people. The body's immune system may react against it. FDA says this risk depends on how it is given. The peptide may clump together, which adds to that risk. Making it may leave unwanted peptide by-products in the product. These points come from FDA's review of compounded drugs. They are not a full list of side effects.

Risks and safety limits

This is not an invitation to experiment. The guide provides no sourcing, reconstitution, injection, cycle, stack, or injury-treatment instructions.

Sports rules · Prohibited

TB-500 is named as a prohibited thymosin-beta-4 derivative on the 2026 WADA Prohibited List and is prohibited at all times for covered athletes.

Reviewed .Check the rules for athletes ↗Read the official rules ↗

Terms used in the studies

molecule
one specific chemical substance
outcome
what the study measured
compounded
made for one patient by a pharmacy, or in batches by a permitted outsourcing facility; a compounded drug is not FDA-approved
mechanism
how a substance may cause a body change
biomarker
a body or lab measurement, not automatically a health benefit
amino acid
a small building block that makes peptides and proteins
indication
the approved or studied use and patient group

Read the sources

Show 3 sources

Review history

Revalidated TB-500 against the 2026 WADA Prohibited List, where TB-500 and thymosin-beta-4 are named in the prohibited growth-factor category.

Initial brief uses FDA's July 2026 identity and evidence review before final agency action.

Not independently medically reviewed. This page is not a dosing, sourcing, or treatment guide.

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