← Compound Library

Thymosin Alpha-1

Thymic Immune Modulator

Also known as: Thymalfasin · Zadaxin · Tα1

An FDA-approved 28-amino-acid thymic peptide that enhances innate & adaptive immunity. Used clinically for hepatitis B/C, cancer adjuvant therapy, & immune deficiency.

Typical Dose

900 mcg–1.6 mg twice weekly

Route

Subcutaneous injection

Cycle

6–12 weeks for acute immune support; longer cycles for chronic immune deficiency

Half-life

~2 hours

Storage

Lyophilized: 2–8°C. Reconstituted: refrigerate, use within 24–48 hours (preservative-free) or 30 days (BAC water).

Overview

Thymosin Alpha-1 (Tα1) is the biologically active N-terminal fragment of Prothymosin-Alpha, naturally produced by the thymus gland. It has been approved in over 35 countries under the brand name Zadaxin for treatment of viral hepatitis, malignancy, & immune reconstitution. The FDA has granted Orphan Drug designation for several indications.

Its mechanism involves upregulation of Toll-like receptors (TLR2, TLR9) on dendritic cells, enhancement of NK cell activity, induction of T-helper cell differentiation (Th1 polarization), & augmentation of cytotoxic T-lymphocyte activity. Unlike immunosuppressants, Tα1 restores immune competence without driving autoimmunity.

In research & wellness use, Tα1 is used during & after acute illness, cancer treatment, or chronic viral infection. It is one of the few peptides with a substantial human clinical evidence base at therapeutic doses.

Quick Start Guide

1

Reconstitute with 1 mL sterile or bacteriostatic water per 1.6 mg vial.

2

Inject 1.6 mg subcutaneously twice weekly (standard Zadaxin protocol) or 900 mcg twice weekly (research protocols).

3

Morning injection preferred for circadian alignment with immune activation.

Research Indications

Immune modulation & reconstitution

Most Effective

Restores NK cell, T-cell, & dendritic cell function in immune-compromised states. Clinical approval in multiple countries.

Viral hepatitis B & C

Most Effective

Zadaxin approved for hepatitis B & C. Reduces viral load & enhances immune clearance in combination with antiviral therapy.

Cancer adjuvant therapy

Effective

Reduces chemotherapy-related immunosuppression & may enhance immune recognition of tumor cells. Used alongside standard oncology protocols.

Acute infection support

Effective

Reduces severity & duration of viral & bacterial infections in immune-competent hosts. Used in COVID-19 severe illness protocols in multiple countries.

Research Protocols

General immune support

6–12 weeks

Dose

900 mcg

Frequency

Twice weekly SubQ

Route

SubQ abdomen

Clinical protocol (Zadaxin)

6 months for chronic hepatitis

Dose

1.6 mg

Frequency

Twice weekly

Route

SubQ

Acute illness support

2–4 weeks

Dose

1.6 mg

Frequency

Daily for 5–7 days, then 2x/week

Route

SubQ

Peptide Interactions

TB-500Compatible

No known interaction. TB-500 handles tissue repair; Tα1 handles immune modulation. Sometimes combined for comprehensive wellness protocols.

BPC-157Compatible

No known adverse interaction. Occasionally combined in post-illness recovery protocols.

Side Effects & Safety

Common

  • Injection site redness or mild swelling
  • Mild fatigue (first 1–2 doses)

Uncommon

  • Headache
  • Low-grade fever (immune activation; typically resolves within 24h)

When to Stop

  • Signs of systemic allergic reaction
  • Active autoimmune disease exacerbation (theoretical concern given immune activation)

How to Reconstitute

1

Wipe stopper with alcohol.

2

Draw 1 mL bacteriostatic water into syringe.

3

Inject slowly down inner vial wall.

4

Swirl gently. Solution should be clear.

5

Refrigerate. Use within 30 days.

Dosing math: 1 mL BAC water per 1.6 mg vial = 1600 mcg/mL. For 900 mcg dose: 0.56 mL. For 1.6 mg: 1.0 mL.

Quality Indicators

Good — use as normal

  • Crystal clear, colorless solution

Acceptable

  • Very slight cloudiness that clears immediately

Discard immediately

  • Persistent cloudiness
  • Particulate
  • Discoloration

What to Expect

Week 1–2

NK cell & dendritic cell upregulation begins within days. Some users report increased energy & reduced susceptibility to opportunistic infections.

Week 3–6

T-cell counts improving in baseline-deficient states. Viral load reduction (if applicable) begins to be measurable.

Week 7–12

Cumulative immune reconstitution. In healthy users, subjective improvements in infection resistance & recovery speed.

Community Insights

Self-reported. Reflects user experience, not clinical outcomes.

Research References

Thymosin alpha1 activates complement receptor-mediated phagocytosis in human monocyte-derived macrophages

Journal of Leukocyte Biology · 2010

Demonstrates Tα1's direct activation of innate immune cells via TLR2/TLR9 pathways.

Thymosin alpha 1 treatment in patients with COVID-19 pneumonia

Frontiers in Pharmacology · 2020

Retrospective analysis showing reduced mortality & faster discharge in severe COVID-19 patients treated with Tα1.

Verify what you have

Information on this page applies to pharmaceutical-grade peptides. Purity & identity of research-grade products vary. Certipep provides independent ESI-TOF-MS & HPLC analysis with a signed analytical report.

Submit a sample