TB-500 (Thymosin Beta-4 Fragment)
Synthetic Fragment (17-23) of Thymosin Beta-4
Community Research
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A synthetic 7-amino acid fragment corresponding to the actin-binding region of thymosin beta-4, originally developed for equine use with retained tissue repair properties. TB-500 acts as principal actin-sequestering protein, regulating cell migration, promoting angiogenesis, reducing inflammation, and activating stem cell differentiation.
Acts as principal actin-sequestering protein, regulating cell migration, promoting angiogenesis, reducing inflammation, and activating stem cell differentiation for comprehensive regenerative effects.
Molecular Data
?SDKPDMAEIEKFDKSKLKKTETQEKNPLPSKETIEQEKQAGESAc
Position 1
Serine
Position 2
Aspartic Acid
Position 3
Lysine
Position 4
Proline
Position 5
Aspartic Acid
Position 6
Methionine
Position 7
Alanine
Position 8
Glutamic Acid
Position 9
Isoleucine
Position 10
Glutamic Acid
Position 11
Lysine
Position 12
Phenylalanine
Position 13
Aspartic Acid
Position 14
Lysine
Position 15
Serine
Position 16
Lysine
Position 17
Leucine
Position 18
Lysine
Position 19
Lysine
Position 20
Threonine
Position 21
Glutamic Acid
Position 22
Threonine
Position 23
Glutamine
Position 24
Glutamic Acid
Position 25
Lysine
Position 26
Asparagine
Position 27
Proline
Position 28
Leucine
Position 29
Proline
Position 30
Serine
Position 31
Lysine
Position 32
Glutamic Acid
Position 33
Threonine
Position 34
Isoleucine
Position 35
Glutamic Acid
Position 36
Glutamine
Position 37
Glutamic Acid
Position 38
Lysine
Position 39
Glutamine
Position 40
Alanine
Position 41
Glycine
Position 42
Glutamic Acid
Position 43
Serine
Position 44
Research Indications
Accelerated healing of muscle fibers with reduced recovery time and enhanced repair via cell migration and differentiation.
Connective tissue repair with reduced scar formation and improved biomechanical properties of healing tissues.
Enhanced dermal closure, improved angiogenesis, and reduced inflammation in acute and chronic scenarios.
Faster recovery from intense training with reduced muscle soreness and improved tissue repair.
Strengthened tissues through enhanced repair mechanisms may reduce injury risk.
Improved muscle quality through enhanced regeneration and repair pathways.
Protective effects against neuronal damage in various models.
Preclinical evidence for improved outcomes in spinal injury models.
Potential neuroprotective and regenerative effects on brain tissue.
Dosing Protocols
Subcutaneous or intramuscular injection. Flexible timing with no empty stomach requirement. Can be injected near injury site for localized effect.
| Goal | Dose | Frequency | Route |
|---|---|---|---|
| General tissue repair | 2-3mg | 2x weekly | SubQ or IM |
| Serious injury recovery | 4-5mg | 3x weekly | SubQ near injury site |
| Athletic enhancement | 2-3mg | 2x weekly | SubQ |
| Chronic conditions | 3-4mg | 2-3x weekly | SubQ or IM |
| Maintenance | 2mg | 1-2x weekly | SubQ |
| Post-surgical recovery | 3-5mg | 3x weekly | SubQ |
Reconstitution Instructions
- Bacteriostatic water (BAC)
- Insulin syringes (1mL recommended)
- Alcohol swabs
- TB-500 vial (2mg or 5mg typical)
- Sterile work surface
- 1 Clean work area and hands thoroughly with alcohol
- 2 Calculate required BAC water volume
- 3 Draw calculated BAC water slowly into syringe
- 4 Inject BAC water slowly down vial side (never directly on powder)
- 5 Gently swirl vial until powder completely dissolves
- 6 Store reconstituted solution refrigerated, use within 28 days
Interactions
What to Expect
Side Effects & Safety
Common Side Effects
- Generally minimal side effects
- Possible mild injection site reactions
- Temporary fatigue in some users
Stop Signs - Discontinue if:
- Persistent or worsening injection site infections
- Unusual swelling or prolonged redness
- Severe allergic reactions
- Unexpected systemic symptoms
- Concerning health changes
Contraindications
- Active cancer treatment (due to angiogenic effects)
- Pregnancy or breastfeeding
- Immunosuppressive medications (consult provider)
- WADA prohibited for competitive athletes
Quality Checklist
Good Signs
- White lyophilized powder - fine, evenly distributed with light fluffy texture
- Clear, colorless solution after reconstitution with no particles
- Proper vacuum seal intact with secure rubber stopper
Warning Signs
- Slight powder clumping acceptable if completely dissolves with gentle swirling
Bad Signs
- Colored or crystalline powder (yellow/brown indicates degradation)
- Persistent cloudiness, floating particles, or precipitation
- Damaged vial seal or contamination signs
References
- The regenerative peptide thymosin beta-4 accelerates the rate of dermal healing in preclinical animal models and in patientsTreadwell, T., Kleinman, H.K., Crockford, D., Hardy, M.A., Guarnera, G.T., Goldstein, A.L.Annals of the New York Academy of Sciences (2012)
In two Phase 2 clinical trials, thymosin beta-4 accelerated healing of chronic pressure ulcers and venous stasis ulcers by almost a month compared to placebo, with confirmed safety and tolerability.
- Development of thymosin beta4 for treatment of patients with ischemic heart diseaseCrockford, D.Annals of the New York Academy of Sciences (2007)
Synthetic thymosin beta-4 given intravenously was well tolerated with no dose-limiting toxicity; promotes cardiomyocyte migration and survival, and stimulates coronary vasculogenesis for cardiac ischemia treatment.
- Evaluation of skeletal and cardiac muscle function after chronic administration of thymosin beta-4 in the dystrophin deficient mouseSpurney, C.F., et al.PLoS One (2010)
Chronic thymosin beta-4 administration increased the number of regenerating skeletal muscle fibers in exercised dystrophin-deficient (mdx) mice, showing potential for Duchenne muscular dystrophy treatment.
- Thymosin beta-4 significantly improves signs and symptoms of severe dry eye in a phase 2 randomized trialSosne, G., Dunn, S.P., Kim, C.Cornea (2015)
Phase 2 randomized trial in 9 severe dry eye patients showed RGN-259 (0.1% thymosin beta-4) eye drops achieved statistically significant improvements in both signs and symptoms, with effects lasting 28 days post-treatment.
- A first-in-human, randomized, double-blind, single- and multiple-dose, phase I study of recombinant human thymosin beta-4 in healthy Chinese volunteersWang, X., et al.Journal of Cellular and Molecular Medicine (2021)
Phase I study in 54 healthy subjects with ascending doses (0.05-25.0 mcg/kg) demonstrated mild to moderate adverse events with no dose-limiting toxicities or serious adverse events.
- 0.1% RGN-259 (Thymosin beta-4) Ophthalmic Solution Promotes Healing and Improves Comfort in Neurotrophic Keratopathy Patients in a Randomized, Placebo-Controlled, Double-Masked Phase III Clinical TrialSosne, G., Kleinman, H.K., Springs, C., Gross, R.H., Sung, J., Kang, S.International Journal of Molecular Sciences (2022)
Phase III trial demonstrated thymosin beta-4 ophthalmic solution promotes corneal healing and improves comfort in neurotrophic keratopathy, advancing toward FDA approval.
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Disclaimer
This information is for educational and research purposes only. Consult a healthcare professional before use.