TB-500
A marketed name for a synthetic thymosin-beta-4-related fragment; product identity and evidence are often conflated with full-length thymosin beta-4.
On this page
WHAT THE EVIDENCE SAYS
TB-500 evidence summary.
The first question for TB-500 is entity identity: evidence about full-length thymosin beta-4 should not be treated as direct evidence for every TB-500 product.
01 / CLASSIFICATION
What is TB-500?
Names, fragments, salts, formulations, routes, and branded products are kept distinct whenever transferring evidence would change the conclusion.
02 / EVIDENCE
TB-500 human and preclinical evidence.
The five-point bars describe the maturity and depth of the evidence base. They do not score effectiveness, safety, or personal suitability.
03 / STATUS
TB-500 FDA and sport status.
Status summaries are educational and time-sensitive. Consult current official labeling and anti-doping resources for a decision.
04 / RESEARCH AREAS
What is TB-500 being studied for?
05 / COMPARISONS
Compare TB-500.
06 / LATEST & DEFINING SOURCES
TB-500 primary and official sources.
07 / QUESTIONS
Questions about TB-500.
Start with identity, research, human evidence, approval, sport status, and the limits of the current record.
The first question for TB-500 is entity identity: evidence about full-length thymosin beta-4 should not be treated as direct evidence for every TB-500 product.
Current source-backed research areas include Actin biology, Tissue repair, Cell migration, Angiogenesis. These areas describe investigation, not established personal benefit.
Current U.S. status for TB-500: Not FDA approved; product identity and peptide-related impurities are material uncertainties.
Current sport-status snapshot for TB-500: Prohibited at all times under the 2026 WADA List (S2).
Name similarity is not evidence equivalence.
Both are promoted for recovery far beyond the human evidence. The main differences are the shape of the preclinical literature and the identity problem around TB-500.