What is TB-500?
TB-500 is described as a fragment, meaning a piece, of thymosin beta-4 (Mendias & Awan, 2026). Thymosin beta-4 itself is a protein of 43 amino acids that the body makes, occurs in almost all cells and is involved in tissue repair, cell migration and inflammation control. The human studies used full thymosin beta-4. In a research context, TB-500 is used for regeneration, tendon and ligament health and mobility.
Unlike BPC-157, which people like to inject locally, TB-500 acts more systemically and distributes well through the body. It ships as a freeze-dried powder you dissolve in bacteriostatic water.
Comparison
TB-500 and its relatives
TB-500 next to the short fragment, the starting piece Ac-SDKP and BPC-157, as stated in the TPD lexicon. Tap a card to open its entry.
Simplified: only full thymosin beta-4 was tested in humans, the fragments and blends not in phase 3. 212
How it works
The compound binds actin, a central building block of the cell skeleton. That way it supports the migration of repair and progenitor cells to a site of damage. On top come effects on the formation of new blood vessels and on dampening inflammation.
In a research context, thymosin beta-4 is studied for wound healing and heart tissue, among others. The effects are spread across the whole body, not just at the injection site.
Where it acts
Where thymosin beta-4 acted in studies
Tap a point or a card. Colour = target, grey = observed. Almost everything from animal studies or with eye drops.
- Skin and wounds
Up to 61 percent more new skin after 7 days, more collagen and vessels (rats)3
Actin - Eye (cornea)
Defect closed with drops in 6 of 10, placebo 1 of 8 (phase 3)7
Observed in trials - Heart
More surviving heart muscle cells and better pump function after infarction (mice)4
ILK - Blood vessels
The actin-binding motif alone was enough for new vessel formation (cells)2
Actin
Known targets2
Compound CHEMBL4594314: two described targets, type of action on each card.
- Gene
- ACTB
- UniProt
- P60709
- ChEMBL
- CHEMBL2062353
- Action
- Binds free actin via a motif of seven amino acids, not a receptor agonist
- Gene
- ILK
- UniProt
- Q13418
- ChEMBL
- CHEMBL5247
- Action
- Forms a complex with PINCH and ILK that switches on the survival signal Akt (mice and cells)
What you need
For subcutaneous use you need:
Supplies
5 things, numbered as in the picture
Tick off what you already have. Vial and BAC water are our real shop photos at the same size.
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TB-500 vial
The TB-500 vial with the freeze-dried powder
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Bacteriostatic water
Bacteriostatic water to dissolve it
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U-100 insulin syringes
U-100 insulin syringes
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Alcohol swabs
Alcohol swabs for the vial cap and the skin
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Sharps container
A sealable sharps container for used needles
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Reconstitution
The powder is dissolved in bacteriostatic water. How much water you add sets the concentration and therefore how many units you draw for your dose on the insulin syringe.
Use the peptide calculator for this: pick your vial size and the water volume to see the concentration and units per dose.
When dissolving, just add the bac water, it does not matter if it hits the powder directly. Then swirl or shake until everything has dissolved, both are fine.
Step by step
Dissolving the powder
Four steps, the same for every vial size.
- 1Wipe the cap
Clean the rubber stopper with an alcohol swab.
- 2Add BAC water
Just add it, it does not matter if it hits the powder directly.
- 3Swirl or shake
Until everything has dissolved, both are fine.
- 4Draw up
With the U-100 insulin syringe.
Injection
Because TB-500 acts systemically, the exact site matters less than with BPC-157. Classically it is injected subcutaneously into the abdomen (keep clear of the area around the navel), the front and the inner side of the thigh or the back of the upper arm.
Injection
Where and at what angle
Pick a spot or switch the angle. Subcutaneous means: into the fat layer, not the muscle.
Rotate the spot each time, never the same one twice in a row.
Rule of thumb: where there is more fat under the skin, insert straight at 90 degrees. In lean people with little fat, 45 degrees, so the needle stays in the fat layer. Simplified diagram.
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Clean the spot with an alcohol swab and let it dry
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Pinch up a small fold of skin
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Insert the needle: at 90 degrees where there is more fat under the skin, at 45 degrees in lean people with little fat
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Inject slowly, wait a moment, then withdraw
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Put the needle straight into the sharps container
Rotate the site.
Dosing
Dosing
Dosing, titration and syringe
Loading the dosing information …
- Getting started and stepping up, drawn as a staircase
- Units on the U-100 syringe for every step
- How long one vial lasts
What the research shows
Thymosin beta-4 is well described mechanistically and was studied in early clinical approaches for wound healing and heart tissue. A review summarises structure, function and clinical potential. For injection under the skin, large approval trials are missing. As eye drops, however, thymosin beta-4 went up to phase 3: for dry eye in the completed trials ARISE-2 (601 participants) and ARISE-3 (700 participants) and for a corneal disease (neurotrophic keratopathy) in a small phase 3 trial with 18 participants (Sosne, 2022). It is not approved so far. TB-500 as a research form is not the same as an approved medicine. That belongs in the picture honestly.
The source with a link is in the source block below.
Study results
What the trials measured
Interactive: switch tabs, tap points, show or hide arms. Arms are named relative to each other, no dosing advice.
Closed corneal defect after 4 weeks7
Share with a fully closed defect in neurotrophic keratopathy, eye drops against placebo
Very small phase 3 trial with 18 participants, stopped early. The difference was just above the significance threshold (p = 0.0656). Two weeks after the drops ended no defect returned in the thymosin group.
Discomfort in the provocation test6
Difference from placebo after 28 days of eye drops, phase 2 with 72 participants
The two primary endpoints (discomfort and staining of the lower cornea on day 29) did not differ. Secondary endpoints such as this value from the provocation test on day 28 were significant.
Wound healing in rats3
More than in the saline control group, applied to the skin or into the abdominal cavity
Animal study with full thymosin beta-4. The wounds also showed more collagen and more new vessels.
Research status
Where the research stands
Shown are the registered trials with full thymosin beta-4: eye drops, a gel for the skin and infusion after heart attack. None of them tests TB-500 under the skin. As of 26 Oct 2026. 11
- Preclinical Wound healing, vessel formation and heart in cells and animals
- Phase 1 2 trials, 2 completed
- Phase 2 10 trials, 6 completed, 3 stopped early
- Phase 3 5 trials, 3 completed, 1 stopped early
- Approval not yet
Show all 15 phase 2 and 3 trials on a timelineHide timeline
NCT00311766 · 30 participants, started Feb 2006, stopped early Jul 2010.
NCT00382174 · 72 participants, started May 2006, primary endpoint reached Dec 2008.
Registry entry ↗ · Results not yet in PubMed
SSVS · NCT00832091 · 72 participants, started Jul 2006, primary endpoint reached Jan 2009.
Registry entry ↗ · Results not yet in PubMed
NCT00598871 · 12 participants, started Dec 2007, stopped early Feb 2009.
NCT01393132 · 9 participants, started Mar 2011, primary endpoint reached Dec 2012.
Registry entry ↗ · Results not yet in PubMed
NCT01387347 · 72 participants, started Aug 2011, primary endpoint reached Oct 2011.
Registry entry ↗ · Results not yet in PubMed
CELEB · NCT03578029 · 4 participants, started May 2019, stopped early Sept 2021.
NCT05485818 · 62 participants, started Nov 2020, primary endpoint reached Sept 2021.
Registry entry ↗ · Results not yet in PubMed
NCT05984134 · 90 participants, started Jul 2022, primary endpoint reached May 2023.
Registry entry ↗ · Results not yet in PubMed
NCT07586865 · 189 participants (planned), started May 2026, primary endpoint planned Aug 2027.
ARISE-1 · NCT02597803 · 317 participants, started Sept 2015, primary endpoint reached Jun 2016.
Registry entry ↗ · Results not yet in PubMed
SEER-1 · NCT02600429 · 18 participants, started Sept 2015, stopped early Nov 2019.
Registry entry ↗ · Results: Sosne et al., International Journal of Molecular Sciences, 2022
ARISE-2 · NCT02974907 · 601 participants, started Nov 2016, primary endpoint reached Sept 2017.
Registry entry ↗ · Results not yet in PubMed
ARISE-3 · NCT03937882 · 700 participants, started May 2019, primary endpoint reached Nov 2020.
Registry entry ↗ · Results not yet in PubMed
SEER-2 · NCT05555589 · 70 participants (planned), started Apr 2023, primary endpoint planned Apr 2026.
Bar: start to primary endpoint (planned for running trials). Green = completed, blue = progress until 26 Oct 2026, grey = stopped early. Phase 1: 2 trials on safety and pharmacokinetics, not shown as bars.
On the skin
Besides the eye drops, thymosin beta-4 was also tested in humans as a gel applied directly to wounds. In two phase 2 trials in leg ulcers and pressure ulcers wound closure was about a month faster in participants whose wounds closed fully (Treadwell 2012). The review comes from the developer's side. All of these studies used the full thymosin beta-4, not the research form TB-500.
Side effects
TB-500 is considered well tolerated. Mostly mild things are reported: injection-site reactions, occasionally brief tiredness after dosing. Solid long-term human safety data are limited, so phases make more sense than continuous running.
Tolerability
Side effects in the phase 2 trial with eye drops
Out of 100 participants, how many had a side effect. Eye drops with thymosin beta-4 against placebo, no injection under the skin.
| Event | Placebo | Thymosin beta-4 |
|---|---|---|
| Any side effect6 | 0% | 0% |
Zero does not mean safe here. Given into a vein, 40 healthy people tolerated thymosin beta-4 for 14 days without serious side effects. There are no solid human data for TB-500 under the skin.6510
Practice
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Run it in phases: loading first, then maintenance, then a break.
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TB-500 is often combined with BPC-157: BPC more locally, TB-500 systemically.
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Sleep, protein and rest support the regeneration.
Storage
The undissolved powder is robust, normal room temperature (around 20 to 25 degrees) is fine, ideally kept in the dark. The reconstituted solution goes into the fridge (2 to 8 degrees) and stays stable there for at least 4 to 6 months with barely any loss of potency, in practice considerably longer. The bacteriostatic water brings a preservative that keeps the dissolved form stable for longer.
Shelf life
How long it keeps
Robust, no fridge needed.
At least 4 to 6 months with barely any loss of potency. The bacteriostatic water brings a preservative.
- Keep it dark
- Dissolved: 2 to 8 degrees
- Note the mixing date on the vial