About Thymosin Alpha-1
Tα1 modulates both innate and adaptive immune responses by stimulating the differentiation and maturation of T-cells, dendritic cells, and natural killer cells. It upregulates MHC class I and II expression, enhancing antigen presentation. It also promotes the production of key cytokines including interferon-γ and interleukin-2, which are central to immune surveillance.
Thymosin alpha-1 (thymalfasin; Zadaxin) is a 28-amino-acid synthetic peptide corresponding to the N-terminal sequence of prothymosin alpha, developed as a biological response modifier with established clinical use outside the United States for chronic viral hepatitis and as an immune adjuvant in cancer and immunocompromised patients. Thymalfasin modulates innate and adaptive immune responses by upregulating Toll-like receptor expression and dendritic cell maturation, enhancing T-helper 1 cytokine signaling, and potentiating antigen-specific T-cell responses in settings of impaired immune function. A prospective multicenter randomized controlled trial demonstrated that combination therapy with thymosin alpha-1 and entecavir improved serological outcomes in HBV-related compensated cirrhosis compared to entecavir alone, and cumulative RCT evidence supports its role as an immune adjuvant in hepatitis B and C treatment. Thymosin alpha-1 is approved in approximately 35 countries — including China, Italy, and other Asian and Eastern European markets — for hepatitis B and hepatitis C adjuvant therapy, but has not received FDA approval in the United States and is available in US-adjacent research contexts only as an investigational compound. Thymosin alpha-1 dosage: in approved clinical protocols (hepatitis B adjuvant therapy), thymalfasin is administered as 1.6 mg subcutaneously twice weekly for 26–52 weeks. This dosing schedule is derived from the pivotal trials conducted by SciClone Pharmaceuticals, which developed Zadaxin. In COVID-19 research during 2020–2021, Chinese clinical centers studied thymosin alpha-1 as an immune adjuvant in severe and critical COVID-19 patients, with published observational and small RCT data; this research context brought renewed attention to the peptide's immune-modulating properties outside the hepatitis indication. Within the recovery and immune-support peptide landscape, thymosin alpha-1 is most closely compared to thymosin beta-4 (TB-500) — the two peptides share the thymosin nomenclature but have distinct mechanisms and research profiles. Thymosin alpha-1 is an immune activator (TH1 upregulation); thymosin beta-4 is primarily studied for tissue repair and actin dynamics. Providers offering immune-modulating peptide compounds are listed in the PeptideBase directory.
Thymosin Alpha-1 Benefits & Research Areas
Research Signals
Commonly researched in the context of
Population research notes
These signals reflect research interest areas, not treatment indications.
Regulatory & Evidence
Risk Profile
Moderate risk profile in research contexts. Review contraindications and administration guidelines before use.
Regulatory Status
- Availability Status
- Research Only
- FDA Status
- Not Evaluated
Approved as Zadaxin in China, Italy, and other countries but NOT FDA-approved. Not on FDA 503A Category 1 bulks list. Research use only in US. Immunomodulatory thymic peptide.
Regulatory status reflects publicly available information and may change. This is not legal or medical advice.
Research Sources
2 sources cited · 1 strong · 1 moderate
1 RCT · 1 Cohort
Combination of entecavir with thymosin alpha-1 in HBV-related compensated cirrhosis: a prospective multicenter randomized open-label study
Expert Opinion on Biological Therapy · 2018
Research in a prospective multicenter randomized trial found that combination therapy with thymosin alpha-1 plus entecavir was well tolerated and showed a tendency to inhibit hepatocellular carcinoma development during the 52-week treatment period compared with entecavir monotherapy in patients with HBV-related compensated cirrhosis, supporting thymosin alpha-1 as an immunomodulatory adjunct to antiviral therapy.
IL-15 Plus Thymosin α1 Reduces Senescent Hepatic CD8(+) T Cells in Hepatocellular Carcinoma via PI3K/AKT Suppression.
J Gastroenterol Hepatol · 2026
# Summary Research found that combining interleukin-15 (IL-15) with thymosin alpha 1 (Tα1) synergistically reduced senescent CD8+ T cells in hepatocellular carcinoma by suppressing overactive PI3K/AKT signaling, thereby restoring anti-tumor immune function and prolonging survival in an aged mouse model. This study demonstrated that the dual approach—rescuing existing senescent T cells while simultaneously replenishing the T cell pool through thymic rejuvenation—represents a more effective strategy than either agent alone for overcoming immune dysfunction in liver cancer.
Thymosin Alpha-1 Side Effects & Safety Considerations
Moderate risk profile. Review all reported considerations carefully before use.
Reported contraindications & considerations
Consult a qualified healthcare professional before making any health decisions. This information is educational only and does not constitute medical advice.
Research Stacks
Browse all →Where to Buy Thymosin Alpha-1 — Providers & Availability
203 providersClinics
10 providers22 Health & Hormone
United StatesView →Alternity Healthcare
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United StatesView →Body Lounge Park Cities
United StatesView →Carvalho Healthcare
United StatesView →Center for Advanced Urology
United StatesView →Denver Wellness & Aesthetics Center
United StatesView →Dr. Erica Oberg
United StatesView →Eunoia Holistic
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Questions to Ask Your Provider
Frequently Asked Questions — Thymosin Alpha-1
Thymosin alpha-1 (thymalfasin; Zadaxin) is a 28-amino-acid synthetic peptide corresponding to the N-terminal sequence of prothymosin alpha, developed as a biological response modifier with established clinical use outside the United States for chronic viral hepatitis and as an immune adjuvant in cancer and immunocompromised patients. Thymalfasin modulates innate and adaptive immune responses by upregulating Toll-like receptor expression and dendritic cell maturation, enhancing T-helper 1 cytokine signaling, and potentiating antigen-specific T-cell responses in settings of impaired immune function.
TH1 immune activation via Toll-like receptor upregulation, hepatitis B and C treatment adjuvant — approved in 35+ countries, dendritic cell maturation and antigen-specific T-cell potentiation, COVID-19 immune support research (2020–2021 Chinese clinical data).
Research on Thymosin Alpha-1 primarily documents effects related to TH1 immune activation via Toll-like receptor upregulation and hepatitis B and C treatment adjuvant — approved in 35+ countries and dendritic cell maturation and antigen-specific T-cell potentiation and COVID-19 immune support research (2020–2021 Chinese clinical data). These are areas covered in preclinical and clinical literature — individual response varies and effects depend on context of use.
Reported contraindications and considerations for Thymosin Alpha-1 include active cancer history. This is educational information only — consult a qualified healthcare professional before use.
203 providers in the directory currently offer Thymosin Alpha-1.
Research in a prospective multicenter randomized trial found that combination therapy with thymosin alpha-1 plus entecavir was well tolerated and showed a tendency to inhibit hepatocellular carcinoma development during the 52-week treatment period compared with entecavir monotherapy in patients with HBV-related compensated cirrhosis, supporting thymosin alpha-1 as an immunomodulatory adjunct to antiviral therapy.
Thymosin Alpha-1 is featured in the following research stacks on PeptideBase: Thymosin Alpha-1 + LL-37: Immune Support.