What happened to the terminated Thymosin Beta-4 trials?
Thymosin Beta 4 is an Actin sequestering peptide. 11 of 26 records administer it, and at lea…
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For Research & Educational Discussion Only. Not Medical Advice
Actin-sequestering peptide
Also known as TB-500, Tβ4, RGN-259
A naturally occurring actin-binding peptide with genuine early clinical work in eye and wound indications. "TB-500" as sold is usually a fragment, not the full peptide, and the two are routinely conflated.
Sold inside: GLOW, KLOW . Named blends. No trial has tested those combinations.
In shortA protein found in most human cells, and in high amounts in platelets and wound fluid. The distinction that gets constantly missed: TB-500 as sold is usually a short fragment, not the full protein. The human trials that exist used the full protein, so citing them to support the fragment is a swap that happens often and is rarely pointed out.
Thymosin beta-4 is a 43-amino-acid peptide found in most human cells and in high concentration in platelets and wound fluid. It is a major intracellular actin-sequestering protein.
An important distinction that most discussion collapses: TB-500 as sold is generally a synthetic fragment, commonly the Ac-LKKTETQ sequence region, not full-length thymosin beta-4. The clinical work that exists, largely from RegeneRx in ophthalmology and dermal wound healing, used the full-length peptide. Citing that work in support of the fragment is a substitution that happens constantly and is rarely flagged.
In shortInside cells it controls the scaffolding that lets cells move, and that part is settled biology. The effects claimed for treatment, growing blood vessels, pulling cells into a wound, calming inflammation and reducing scarring, are much less pinned down, and nobody has definitively identified what it binds to outside the cell.
The characterised intracellular function is sequestration of G-actin monomers, regulating actin polymerisation and therefore cell motility, and this is well established as cell biology.
The extracellular effects proposed for therapeutic use, promotion of angiogenesis, cell migration into wounds, modulation of inflammatory signalling, and reduction of fibrosis, are less well characterised, and the receptor or receptors mediating extracellular activity are not definitively identified. The heptapeptide region is the fragment usually credited with the actin-binding activity, which is the basis for using it in place of the whole molecule.
In shortEarly human work, in narrow uses, with the full protein. Trials in dry eye and a corneal condition reported signals, with mixed results. Wound healing work stopped at early stages. For the muscle and recovery uses that dominate discussion there is no properly sized human evidence, for either the full protein or the fragment.
Early clinical, in narrow indications, using the full-length peptide.
Randomised trials in dry eye disease and in neurotrophic keratopathy have reported signals on ocular surface endpoints, with mixed results across trials and endpoints. Work in dermal wound healing, including venous stasis and diabetic ulcers, has produced early-phase results without a definitive programme.
For the musculoskeletal and recovery uses that dominate community discussion, there is no adequately powered human evidence for either the full peptide or the fragment. Preclinical cardiac work in animal infarct models is frequently cited and has not translated into completed human outcome trials.
In shortMost human safety data comes from eye drops and creams, which says little about injecting it. The concerns are the same as for anything that grows blood vessels and moves cells around: an undiagnosed cancer, and unknown effects of long exposure. No long-term data exists, and it is banned in sport. Given the full-protein versus fragment confusion, not knowing what you have is not hypothetical here.
Human safety data comes mostly from topical and ophthalmic formulations, where tolerability has generally been acceptable. That does not transfer to systemic administration.
Mechanistically the concerns are the same family as any pro-angiogenic and pro-migratory agent: effects on undiagnosed malignancy, and unknown consequences of sustained systemic exposure. No long-term systemic safety data exists.
Prohibited in sport under WADA's S2 category. Material sold as TB-500 is research-grade with unverified identity. And given the full-peptide/fragment confusion, "unverified identity" is not a theoretical concern here.
In shortNot approved for human use anywhere. The full protein has held investigational status in eye programmes. TB-500 as sold is a research chemical, and it is banned in sport.
Not approved for human use in any major jurisdiction. Full-length thymosin beta-4 has held investigational status in ophthalmology programmes. TB-500 as sold is a research chemical, prohibited in sport.
2 studies indexed. Findings and limitations get equal weight, on purpose.
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Everything above is free to read. What an account opens is the evidence underneath it: 2 studies with their limitations, and the regimen each trial actually reported.
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Reading is free, an account is not the same as paying. 43 compound guides, every study with its limitations written underneath, and the regimens those trials actually used. A free account opens all of it. A membership is a separate decision, and it opens the forum. What membership costs.
The wider literature
16 indexed papers and 11 registered trials mentioning Thymosin Beta-4, straight from PubMed and ClinicalTrials.gov. 11 of 11 administer it; the rest measure it. These have not been read by us. Unlike the studies above, they carry no findings and no limitations written by anyone here, because writing either would mean claiming a reading nobody has done. They are a starting point for yours.
Hudson Biotech2026NCT07487363
interventionalphase1phase2recruitingn=80
ReGenTree, LLC2023NCT05555589
interventionalphase3recruitingn=70
RegeneRx Biopharmaceuticals, Inc.2019NCT01311518
interventionalphase2withdrawnn=0
ReGenTree, LLC2019NCT03937882
interventionalphase3completedn=700
ReGenTree, LLC2016NCT02974907
interventionalphase3completedn=601
ReGenTree, LLC2015NCT02600429
interventionalphase3terminatedn=18
ReGenTree, LLC2015NCT02597803
interventionalphase2phase3completedn=317
ReGenTree, LLC2011NCT01387347
interventionalphase2completedn=72
Michigan Cornea Consultants, PC2011NCT01393132
interventionalphase2completedn=9
ReGenTree, LLC2007NCT00598871
interventionalphase2terminatedn=12
RegeneRx Biopharmaceuticals, Inc.2006NCT00832091
interventionalphase2completedn=72
Di H, et al.Peptides2026PMID 41570941
journal articlereview
Mendias CL, et al.Sports medicine (Auckland, N.Z.)2026PMID 41966639
journal articlereview
Li Y, et al.The Journal of allergy and clinical immunology2025PMID 39978686
journal article
Zeng PM, et al.Stem cell reports2025PMID 40816274
journal articleresearch support, non-u.s. gov't
Chen X, et al.Signal transduction and targeted therapy2025PMID 39837870
journal articleresearch support, non-u.s. gov't
Li Q, et al.Nature communications2023PMID 37696839
journal articleresearch support, n.i.h., extramuralresearch support, non-u.s. gov'tresearch support, u.s. gov't, non-p.h.s.retracted publication
Wang M, et al.Journal of neuroinflammation2021PMID 34183019
journal article
Kassem KM, et al.Canadian journal of physiology and pharmacology2019PMID 30854877
journal articlereview
Sosne GExpert opinion on biological therapy2018PMID 30063853
journal articlepersonal narrativereview
Hinkel R, et al.Expert opinion on biological therapy2018PMID 30063857
journal articleresearch support, non-u.s. gov'treview
Pipes GT, et al.Vitamins and hormones2016PMID 27450736
journal articlereview
Kleinman HK, et al.Vitamins and hormones2016PMID 27450738
journal articlereview
Kim J, et al.Vitamins and hormones2016PMID 27450733
journal articlereviewresearch support, non-u.s. gov't
Kim J, et al.International journal of molecular sciences2015PMID 26006229
journal articleresearch support, non-u.s. gov'treview
Sun HQ, et al.Annals of the New York Academy of Sciences2007PMID 17495248
journal articleresearch support, n.i.h., extramuralresearch support, non-u.s. gov'treview
Horecker BL, et al.Methods in enzymology1985PMID 4088088
comparative studyjournal article
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Thymosin Beta 4 is an Actin sequestering peptide. 11 of 26 records administer it, and at lea…
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For Research & Educational Discussion Only. Not Medical Advice
This guide is educational reference material compiled from published literature. It is not medical advice, not a recommendation, and not a substitute for a clinician who knows your history. Nothing here should be used to make a decision about your own health without one.
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