TB-500
Synthetic fragment related to thymosin beta-4. Investigated in animal studies for cellular migration and tissue remodeling.
Educational only — not medical advice. SmartPeptide does not prescribe, diagnose, or treat. Always consult a licensed healthcare provider before using any peptide, supplement, medication, or protocol.
What the research shows
Animal studies suggest cellular migration and tissue remodeling effects, especially in cardiac and dermal wound models.
What's still experimental
Human efficacy is essentially unproven. Safety profile in humans is undocumented in peer-reviewed RCTs.
Anecdotal / community reports
Athletic recovery claims are common in community forums but not supported by published human trials.
Anecdotal reports are NOT scientific evidence. They reflect personal experience and may not generalize.
FDA approval status
Source: openFDA + DailyMed (NIH/NLM)Doses studied in research
Source: Published clinical trialWhat published trials tested or FDA-approved labels specify. Reporting research facts — not a SmartPeptide recommendation.
The doses below are aggregated from research-peptide community forums (Reddit, biohacker discussions). They are NOT supported by clinical trials, NOT FDA-approved, and NOT a SmartPeptide recommendation. Source purity, dose accuracy, and user-reported outcomes are unverifiable. We display this only because the information is publicly available elsewhere — visitors should absolutely consult a licensed clinician familiar with experimental peptides before any use.
Notes from the source: No human RCT exists. Anecdotal protocols vary widely. Source purity for grey-market TB-500 is unverifiable without independent lab testing.
How clinicians typically protocol this
Third-party reference · not our recommendationDosing phases, cycle lengths, and administration timing as listed in a compounding-pharmacy clinician reference guide. Shown so you can see what a real protocol looks like — and bring informed questions to a licensed clinician.
Dose numbers, frequencies, and cycle lengths in this panel are extracted from a clinician-facing reference protocol distributed by a US-based compounding pharmacy in November 2025. SmartPeptide has paraphrased all descriptive text and adds no endorsement. Always consult a licensed clinician.
Synthetic fragment of Thymosin Beta-4; studied for regenerative and cell-migration effects.
Protocol phases
AM
Varies with health status; no fixed cycle in the reference.
FDA enforcement & recalls
Live · openFDA Drug Enforcement APIMechanism & targets
ChEMBL · UniProt · Open TargetsMolecule (ChEMBL)
View on ChEMBL- CHEMBL3143inhibitorCoagulation factor VIII inhibitor
Protein targets (UniProt)
- Large ribosomal subunit protein bL12mP52815gene: MRPL12Homo sapiens· 198 aaReviewed
As a component of the mitochondrial large ribosomal subunit, plays a role in mitochondrial translation (PubMed:23603806). When present in mitochondria as a free protein not associated with the ribosome, associates with mitochondrial RNA polymerase POLRMT to activate transcription (PubMed:22003127). Required for POLRMT stability (PubMed:26586915)
- Large ribosomal subunit protein uL30Q5SHQ6gene: rpmDThermus thermophilus (strain ATCC 27634 / DSM 579 / HB8)· 60 aaReviewed
Live research
PubMed · ClinicalTrials.gov · Europe PMC · OpenAlexClinical trials (ClinicalTrials.gov)
- Comparative Study of Thymosin Beta 4 Eye Drops vs. Vehicle in the Treatment of Severe Dry EyeCOMPLETEDNCT01393132 · PHASE2 · n=9 · 2011-03
- Study of Thymosin Beta 4 in Patients With Pressure UlcersCOMPLETEDNCT00382174 · PHASE2 · n=72 · 2006-05
- Assessment of the Safety and Efficacy of RGN-259 Ophthalmic Solutions for Dry Eye Syndrome: ARISE-1COMPLETEDNCT02597803 · PHASE2, PHASE3 · n=317 · 2015-09
- Efficacy and Safety Study of Thymosin Beta 4 in Patients With Acute Myocardial InfarctionCOMPLETEDNCT05984134 · PHASE2 · n=90 · 2022-07-15
- Study of Thymosin Beta 4 in Patients With Venous Stasis UlcersCOMPLETEDNCT00832091 · PHASE2 · n=72 · 2006-07
Europe PMC — 5,208 additional records
Includes EU/UK studies and PubMed Central full-text articles. Often surfaces research weeks before PubMed indexes it.
- Understanding the effects of ciprofloxacin on corneal epithelial cells: a study using electric cell-substrate impedance sensing (ECIS) technologyBanga L, Shawky M, Ebrahim F, et al. · 2026
- Peptides for Targeting Chondrogenic Induction and Cartilage Regeneration in OsteoarthritisLiao HJ, Chen HT, Chang CH., et al. · 2026Open access· cited 12×
- Peptides in Regenerative Medicine: A Comprehensive Review of Clinical Applications in Tissue Repair and Chronic Pain ManagementLuansritisakul C, Chiang MC, Burns SL, et al. · 2026
- Recombinant human Thymosin β4 ameliorates experimental colitis and intestinal fibrosis through suppression of mineralocorticoid receptor signalingZhao TR, Hu EB, Wang MW, et al. · 2026
Research volume (OpenAlex topic graph)
Human clinical evidence
Semantic Scholar · AI TLDRs · influence-rankedHuman-study summaries for “thymosin beta-4” are available on Semantic Scholar but the shared free-tier API quota is exhausted right now. Try refreshing in a few minutes, or check the PubMed and Europe PMC panels above for the same literature.
Research funding & verification
NIH RePORTER · CrossRef DOI registryNIH-funded research
U.S. National Institutes of Health- 1RC3HL103357-01$3.0MNonclinical Studies to Advance Novel Drug for Post-STEMI Cardiac RegenerationHynda Karen Kleinman · REGENERX BIOPHARMACEUTICALS, INC. · FY2010
- 2P50DK044757-16$956KFibrotic Sequelae of Childhood Renal DiseasaeAGNES B. FOGO · VANDERBILT UNIVERSITY · FY2007
- 5P50DK044757-20$935KFibrotic Sequelae of Childhood Renal DiseasaeAGNES B. FOGO · VANDERBILT UNIVERSITY · FY2011
- 5P50DK044757-19$935KFibrotic Sequelae of Childhood Renal DiseasaeAGNES B. FOGO · VANDERBILT UNIVERSITY · FY2010
Publication landscape
CrossRef · DOI registry- National Natural Science Foundation of China2,364 works
- National Institutes of Health1,090 works
- Deutsche Forschungsgemeinschaft414 works
- National Science Foundation371 works
- National Research Foundation of Korea337 works
- DOE309 works
Funder diversity is a credibility signal. Research concentrated in a single drug company's funding warrants more scrutiny than research funded across NIH, charities, and academic grants.
Preprints — cutting edge
bioRxiv · medRxiv · via Europe PMCPreprints have NOT been peer-reviewed. They are early research shared by authors before formal validation. Treat findings as preliminary.
- PreprintThymosin Beta-4 and TB-500 in Tissue Healing, Regeneration, and Musculoskeletal Repair: A Scoping ReviewMcGuire F, Hughes E, Maak T, et al. · 2026-05-18
- PreprintEvaluation of Research Grade Peptides Marketed Directly to Consumers Reveals Extensive Variability in Purity and Measured AbundanceMendias CL, Awan TM. · 2026-04-24 · cited 1×
- PreprintSafety and Efficacy of Approved and Unapproved Peptide Therapies for Musculoskeletal Injuries and Athletic PerformanceMendias CL, Awan TM. · 2026-04-07
- PreprintSafety and Efficacy of Approved and Unapproved Peptide Therapies for Musculoskeletal Injuries and Athletic PerformanceMendias CL, Awan TM. · 2025-12-12
- PreprintVincristine treatment reverses podocyte damage in focal segmental glomerulosclerosisMason WJ, Chandler JC, Pomeranz G, et al. · 2024-11-15
- PreprintLocal inflammation at the salmon louse (Lepeophtheirus salmonis) attachment site drives copepodid rejection in Coho Salmon (Oncorhynchus kisutch)Sveen L, Fast MD, Tengs T, et al. · 2024-09-23
Known risks
Almost no human clinical data. Banned in competitive sport (WADA).
Reported side effects
Limited human safety reporting; theoretical immunomodulation concerns.
FDA adverse event reports (FAERS)
Updated quarterly by FDAMost-reported reactions
- Adverse Drug Reaction1
- Malignant Lymphoid Neoplasm1
- Product Dispensed By Unauthorised Provider1
Counts from FDA Adverse Event Reporting System (FAERS). Voluntary reports — they show what was reported, not whether the drug caused the event. Many reports lack confirmation. FAERS docs
What requires medical supervision
Banned in competitive sport (WADA). Not approved for human use in most countries. Clinical supervision required if used at all.
Questions for your clinician
- Is there any human safety data we can review?
- Could this interact with my current medications?
- What objective markers would we follow if we tried this?