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Healing & recoveryAnti-aging & longevity

Thymosin alpha-1

Tα1 · Thymalfasin · Zadaxin (brand)

Approved for another indicationReviewed 12 Aug 2026

Thymosin alpha-1 is a 28-amino-acid peptide originally isolated from the thymus, the organ that trains T cells. It is genuinely a medicine in much of the world: approved in over thirty countries as thymalfasin, principally for chronic hepatitis B, and used in some settings for sepsis and as a vaccine adjuvant.

It is not approved in the United States, which puts it in an unusual position: a compound with substantial clinical use and published trials, sold domestically as a research chemical because the approval happens to be somewhere else.

Unlike TB-500, which is a fragment of a different thymic protein and has no human data, thymosin alpha-1 is the full peptide with real clinical evidence behind it. The names are similar enough that they get conflated constantly, and they are not comparable in evidence.

How it works

Thymosin alpha-1 acts on Toll-like receptors on dendritic cells and influences T cell maturation, pushing the immune response toward a Th1 pattern, the arm that deals with intracellular pathogens and abnormal cells.

It is an immune modulator rather than an immune stimulant, which is a meaningful distinction: the reported effect is on how the response is shaped rather than simply how strong it is. That is also why the caution around autoimmune disease is a genuine one rather than boilerplate.

Regulatory status — United States

Approved as thymalfasin in more than thirty countries, principally for chronic hepatitis B. Not approved in the United States, where it is sold as a research chemical with no manufacturing standard behind it.

Last reviewed 12 Aug 2026. Regulatory positions in this category change frequently; we date this line so you can see how current it is.

What it is studied for

Each entry states the evidence behind it. We do not rank indications by effectiveness — for most compounds here, that would be a claim nobody can support.

Chronic hepatitis B

Clinical trial

The main approved indication.

EvidenceClinical trials supporting approval in over thirty countries.

Sepsis

Clinical trial

Studied as an adjunct in severe infection.

EvidenceRandomised trials with mixed results. An area of ongoing study, not a settled use.

General immune support

Community practice

The reason it is used in this community.

EvidenceNot studied as an endpoint in healthy adults. Extrapolated from use in disease states.

Identity and clearance

Molecule

Class
Thymic peptide, immune modulator
Molecular weight
3108.3 Da
Length
28 amino acids

The full naturally occurring peptide, not a fragment. That is what distinguishes it from TB-500.

Pharmacokinetics

Clinical trial
Half-life2 h
Substantially cleared12 h
100%50%25%0%half-life 2hdose3h6h9h12h
Modelled from the half-life above, assuming first-order elimination. Illustrative rather than measured — it shows the shape of clearance, not a prediction for any individual.

Short-acting. That is why approved regimens use twice-weekly subcutaneous dosing over months.

Dose protocols reported in sources

Displayed for reference only. Every row says where it came from, and a trial protocol and a community convention are not the same kind of information. None of this is fed into the calculator, and none of it is a recommendation.

Dose protocols reported in sources, with the source of each.
GoalDoseFrequencyRouteUnits, 5 mg vialSourceStart this protocol
Approved regimen for hepatitis B1.6 mgTwice weekly for six monthsSubcutaneous64 uClinical trialStart this
Commonly described for general use450 mcg – 1.6 mgTwo or three times weeklySubcutaneousBelow the approved regimen, and for an indication that has not been studied.18–64 uCommunity practiceStart this

Start this copies a row into a protocol of your own, which you can then edit. Where a source gave a dose range or an ambiguous frequency, those fields arrive empty — we will not pick a number on your behalf.

CheckRows marked community practice describe what people commonly do, drawn from public discussion. They are not derived from any trial and are not evidence that a dose is safe or effective.

Calculator

Work out what to draw

Pre-filled with a 10 mg vial as a worked example. These are not recommended values — change them to match the vial in front of you.

Dose unit
Your syringe
010203040506070809010032 units0.32 mL

Draw to 32 units on a 1 mL U-100 syringe. That is 0.32 mL, containing 1.6 mg of Thymosin alpha-1.

Concentration5mg / mL
Volume drawn0.32mL
Doses per vial6.3doses
Per unit50mcg / unit

32 units sits exactly on a printed line.

Bioalmanac performs arithmetic on values you enter. It does not recommend doses, schedules or compounds, and nothing here is medical advice. Confirm every calculation against your vial and syringe before drawing, and speak with a licensed healthcare provider.

Open this calculation in the full calculator

Units, concentration, bacteriostatic water — the glossary defines the vocabulary, and a unit is not a fixed volume.

Safety

Reported effects

  • Injection site redness or discomfortClinical trial

    Common in trials

    The most frequently reported effect, and generally mild.

  • Transient fatigueCommunity practice

    Occasionally reported

  • Generally well toleratedClinical trial

    Documented across trials

    Its tolerability in clinical use is one of the better-established things about it.

When to stop

  • Any new joint pain, rash, or unexplained fever. These can be early signs of immune activation going the wrong way.
  • Any allergic response: rash, hives, facial swelling or difficulty breathing. Seek urgent care.
  • A flare of any existing autoimmune condition.
  • Signs of infection at an injection site.

Interactions and situations that need care

  • Autoimmune diseaseAvoid

    This modulates T cell responses toward a more active pattern. In a condition where the immune system already attacks the body's own tissue, pushing that direction is the specific thing you would not want, and it has not been studied.

  • Immunosuppressant therapy or transplantAvoid

    Immunosuppression after a transplant exists to prevent rejection. An immune modulator works directly against that, and the consequence of getting it wrong is organ loss.

  • Pregnancy and breastfeedingAvoid

    No reproductive or developmental safety data.

What to expect

  • The clinical evidence concerns hepatitis B and sepsis, in people with those conditions. General immune support in healthy adults is not what was studied.
  • Approved regimens run for months, not weeks. In its evidenced use this is not a short course.
  • Its tolerability is well established, which is genuinely unusual for anything on this site.
  • Material sold in the United States is not the approved product, so the trial evidence does not follow it.

Storage and handling

Freeze-dried powder
Refrigerated at 2–8 °C, protected from light.
After mixing
Refrigerated at 2–8 °C. Do not freeze once mixed.
Long-term, frozen
Unopened powder is stable at −20 °C or colder.

Printable one-pagerHow to reconstitute a vial, step by step

With other peptides

  • Thymalincaution

    Thymalin is an undefined calf thymus extract, and thymosin alpha-1 was originally identified as a component of exactly that kind of preparation. Running both is probably taking the same thing twice, once in a known quantity and once in an unknown one.

  • Thymulincaution

    Both are thymic peptides acting on T-cell function. Thymosin alpha-1 has registered clinical use in several countries and thymulin has none, so running both adds an unstudied compound to a studied one for overlapping effect.

Check this against a whole stack

Checking your vial

Research chemicals carry no manufacturing standard, so what the vial looks like is often the only quality signal available before you use it. More on assessing quality and COAs.

  • White cake, clear solution

    Standard for a peptide of this size.

  • Collapsed cake or cloudy solution

    Indicates heat damage or degradation.

Questions

Is thymosin alpha-1 the same as TB-500?
No, and the confusion is common. Thymosin alpha-1 is a full 28-amino-acid peptide with clinical trials and approvals in over thirty countries. TB-500 is a fragment of thymosin beta-4 — a different protein — and it has no completed human trials. Similar names, entirely different evidence.
Why is it not approved in the United States?
It holds approvals in more than thirty countries but has not completed the US regulatory pathway for its indications. That is a regulatory fact rather than a safety finding.

References

  1. Thymosin alpha-1: from bench to bedside, clinical development and use

    Annals of the New York Academy of Sciences / review literature, 2012 · Review of clinical trials and approved use

    Humans

    Reviews approval for chronic hepatitis B across multiple jurisdictions, trial evidence in sepsis and as a vaccine adjuvant, and a consistently favourable tolerability profile.

  2. Commonly reported community protocols

    Bioalmanac editorial summary of public community sources, 2026 · Not a study

    Summarises dose ranges described for general immune use, an indication with no supporting trials. Carries no evidential weight.

Keep this page honest

If something here is wrong, out of date, or missing a source, tell us and we will fix it and say that we did.

Suggest a correction

This page is educational. It describes what published research reports, not what you should do. Peptides discussed here are largely not approved for human use, and nothing on Bioalmanac is medical advice. No clinician reviews these pages.

Page last updated 12 Aug 2026