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Protocolos
Compounds › Immune

Thymosin alpha-1 (TA1)

Immune modulator registered outside the US

Partially approvedImmune

Experimental material. Read before using anything from here.

Nothing on this page is a medical recommendation, prescription or treatment plan. It is an organized translation of protocols circulating in research communities and, where it exists, of what published trials tested. The two are marked differently — and they are not equivalent.

Most of the compounds here have no FDA approval for human use. Several are sold labeled "research use only", which means they have not gone through purity, sterility or dosage controls for human consumption. A community-reported dose is not a validated dose: it is what someone reported having done.

Talk to a licensed health professional before considering any of these compounds. If you already use one and feel anything unexpected, seek care — do not wait for the next routine test.

Summary

28-amino-acid peptide produced naturally by the thymus. It helps train and coordinate the immune cells that fight viruses and other infections. The synthetic version, thymalfasin, is sold as Zadaxin and is registered in several countries for hepatitis B and C.

Quick reference

Route
Subcutaneous — abdomen, thigh or arm. Rotate the sites.
Standard schedule
1.6 mg 2×/week, with a 3–4 day interval (e.g., Monday and Thursday).
Measure
10 mg vial + 2 mL of bacteriostatic water (5 mg/mL): 1.6 mg = 0.32 mL = 32 units on the U-100.
Status
Approved as Zadaxin in more than 35 countries; not approved in the US.

Thymosin Alpha-1 Schedule

Thymosin Alpha-1 Schedule
ParameterValue
Dose per injection1.6 mg
Frequency2x per week
Spacing3-4 days apart (e.g., Mon/Thu)
RouteSubQ
Typical duration6 months (HBV monotherapy / cancer adjunct); up to 12 months (HCV combination)

Thymosin Alpha-1 Schedule

Thymosin Alpha-1 Schedule
Body weightApproximate dose
30 kg1.2 mg 2×/week
35 kg1.4 mg 2×/week
≥40 kg1.6 mg 2×/week (adult, standard)

Cycle Guidelines

Cycle Guidelines
Research contextReported durationSource type
Chronic hepatitis B (monotherapy)6 monthsZadaxin pooled analysis of 3 RCTs
Chronic hepatitis C (with interferon)6-12 monthsZadaxin pooled analysis (2 RCTs + 1 historical control)
Severe sepsis (TESTS, BMJ 2025)7 days continuous (every 12 hours)Phase 3 RCT, 22 Chinese centers
Immune support / community use4-12 weeksCommunity-derived, not from a clinical trial

Thymosin Alpha-1 Reconstitution Guide

Thymosin Alpha-1 Reconstitution Guide
Vial sizeBAC water addedConcentrationVolume per 1.6 mgUnits (U-100 syringe)
5 mg1 mL5 mg/mL0.32 mL32 units
10 mg2 mL5 mg/mL0.32 mL32 units
10 mg1 mL10 mg/mL0.16 mL16 units
20 mg2 mL10 mg/mL0.16 mL16 units
20 mg4 mL5 mg/mL0.32 mL32 units

Thymosin Alpha-1 Timeline & What to Monitor

Thymosin Alpha-1 Timeline & What to Monitor
EndpointWhen measuredSource
Peak plasma TA1 level1-2 hours post-injectionRost et al. 1999 PK study
Lymphocyte / CD4+ shifts4-8 weeks of dosingMultiple HBV/HCV trials
HBV viral load reduction12-26 weeksZadaxin pooled HBV monotherapy analysis
HCV sustained viral response (with interferon)Up to 12 months post-treatmentZadaxin combination-therapy analyses

Thymosin Alpha-1 vs TB-500, BPC-157, and KPV

Thymosin Alpha-1 vs TB-500, BPC-157, and KPV
PeptideMechanismBest-supported research contextEvidence base
Thymosin Alpha-1TLR2/TLR9 → dendritic cells → T-cell activationChronic HBV/HCV, cancer adjunct, immune supportApproved in 35+ countries; decades of clinical use
TB-500 (thymosin beta-4 fragment)Actin-binding peptide; cell migration and tissue repairSoft-tissue and tendon repair (mostly preclinical)Strong animal data; limited human trials
BPC-157Gastric pentadecapeptide; angiogenic and tissue repairGI healing, soft-tissue repairStrong animal data; limited human trials
KPVα-MSH C-terminal tripeptide; anti-inflammatoryGut inflammation, topical skinMechanism clear; small clinical footprint

Storage and handling

The rules below apply to practically every lyophilized peptide in this reference. Where a compound has its own requirement, it appears in the table in the previous section.

  • Lyophilized powder, sealed: refrigerator, between 2 and 8 °C, protected from light. Many tolerate room temperature for short transport periods, but that is tolerance, not a recommendation.
  • After reconstitution: always refrigerated, between 2 and 8 °C. The stability window drops to days or a few weeks, depending on the compound.
  • Never freeze after reconstituting. The freeze–thaw cycle degrades the peptide.
  • Do not shake. Swirl the vial slowly. Shaking breaks the peptide chain.
  • Bacteriostatic water down the wall of the vial, in a slow stream, not squirted directly onto the powder.
  • Cloudy solution, with particles or a color change: discard. There is no recovery.

Lab tests and monitoring

This list is the one that appears recurrently in the source, with small variations by compound. It serves as a starting point for a conversation with a professional — not as a substitute for that conversation.

  • Before starting: complete blood count, comprehensive metabolic panel, lipid panel, fasting glucose and HbA1c, TSH and free T4, blood pressure and resting heart rate.
  • Depending on the compound: IGF-1 (GH axis), lipase and amylase (VIP and the incretin agonists), serum copper and ceruloplasmin (GHK-Cu and blends containing it), CRP.
  • Reassessment: most protocols review between week 4 and week 8, and then every 8–12 weeks.
  • Do not wait for the routine lab test in the face of abdominal pain, visual changes, a change in a mole, shortness of breath, asymmetric swelling or any new and persistent symptom. That is a reason to seek care, not a spreadsheet item.

Evidence limits

What these numbers are and what they are not. The values above were preserved exactly as they appear in the source, without reinterpretation. What the source describes as community practice is marked as such in the tables; what came from a published trial is too. A dose repeated by many people does not become a validated dose by repetition.

Data source: peptidedosingprotocols.com, accessed on September 3, 2026. Translation and organization in Portuguese are original work. No primary source (PubMed, trial registry, package insert) was checked in building this page — the check was against the secondary source, and that alone.

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