— THYMIC IMMUNOMODULATORY PEPTIDE · ANTIVIRAL & IMMUNE SUPPORT

Thymosin Alpha-1.

Thymosin alpha-1 (TA-1) is a 28-amino acid peptide derived from prothymosin alpha in the thymus, approved in over 35 countries as Zadaxin for hepatitis B and C — the most clinically validated peptide in the research market.

Key Signals
Immunity · Antiviral · Immunomodulation
Origin
Synthetic (prothymosin alpha fragment)
Investigator
Goldstein et al. (George Washington), 1977
Class
N-acetylated thymic immunomodulatory 28-mer
Status (UAE)
Research compound (off-label)
— THE RESEARCH STORY

The Thymus's Signal, Now Approved in 35 Countries

Goldstein's group isolates thymosin alpha-1 from calf thymus in 1977, identifying it as the immunologically active fraction of thymosin fraction 5.

Zadaxin (synthetic TA-1) gains approval in over 35 countries for hepatitis B and C — the most extensive regulatory footprint of any research-market peptide.

Research expands to cancer immunotherapy and COVID-19, where TA-1 is used as an immune adjuvant in Chinese clinical protocols.

— T-CELL COUNT RESTORATION
CONCEPTUAL · CD4+ T-CELLS (CELLS/μL) · WEEKS OF TREATMENT
100% 115% 130% 145% WK 2 WK 4 WK 6 WK 8 WK 12
TA-1 TREATED UNTREATED CONTROL
— THE MOLECULE

Twenty-eight residues, the thymus in a vial.

PRIMARY STRUCTURE

Ac-Ser-Asp-Ala-Ala-Val-Asp-Thr-Ser-Ser-Glu-Ile-Thr-Thr-Lys-Asp-Leu-Lys-Glu-Lys-Lys-Glu-Val-Val-Glu-Glu-Ala-Glu-Asn

C₁₂₉H₂₁₅N₃₃O₅₅ · MW 3108.4 Da

3108.4MOLECULAR WEIGHT Da
28AMINO ACIDS
35+COUNTRIES APPROVED

Thymosin alpha-1 is derived from prothymosin alpha in thymic epithelial cells — a 28-residue immunomodulatory sequence driving T-cell maturation, dendritic cell activation, and Toll-like receptor signalling.

— AN HONEST READING OF THE DATA

Genuine drug approvals, not in the US or UAE.

Approved as Zadaxin in 35+ countries; no FDA, EMA, or MOHAP approval for any indication.

TIER 01 / PRECLINICAL
Consistent Animal Evidence
  • T-cell maturation confirmed
  • NK cell activation shown
  • Dendritic cell stimulation
  • TLR9 agonism established
  • Apoptosis induction (tumour models)
TIER 02 / HUMAN DATA
Approved Indication Data
  • HBV: viral load reduction (Zadaxin)
  • HCV: SVR improvement (Zadaxin)
  • Cancer adjuvant (Asian RCTs)
  • COVID-19 adjuvant (China protocols)
TIER 03 / SPECULATIVE
Emerging Applications
  • Long COVID immune restoration
  • Autoimmune condition modulation
  • Immunosenescence (anti-aging)
  • Post-chemotherapy immune recovery
— THYMOSIN ALPHA-1 (TA-1) MECHANISMS & RESEARCH DOSING READY

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— REGULATORY LANDSCAPE

Approved in 35+ Countries, Not in the US or UAE

In the UAE, research-grade peptides occupy a defined regulatory category distinct from licensed medicines. Compounds sold under this classification — including those offered by Dubai Peptides — are intended exclusively for qualified research applications, not for human administration.

Thymosin alpha-1 (Zadaxin) holds marketing approval in over 35 countries for chronic hepatitis B and C, and as a cancer immunotherapy adjuvant in several Asian and Eastern European jurisdictions. Neither the FDA, EMA, nor MOHAP has approved it. A separate off-label market for the research-grade compound exists in the UAE, distinct from Zadaxin's regulated distribution and outside the research-use classification this platform follows.

1977 / DISCOVERY

Goldstein's group isolates thymosin alpha-1 from calf thymus, identifying it as the immunologically active fraction of thymosin fraction 5.

1990s / FIRST APPROVAL

Zadaxin (synthetic TA-1) receives marketing approval in Italy for hepatitis B, marking the first regulatory approval of a thymic peptide drug.

2000s–PRESENT / GLOBAL EXPANSION

Chinese regulatory authorities approve Zadaxin for hepatitis C and cancer immunotherapy — extending the compound's approved indications to over 35 countries.