Age and research-use confirmation
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Thymosin Alpha-1, 28-aa thymic peptide
A 28-amino acid thymic peptide that modulates innate and adaptive immunity via TLR signaling, one of the most clinically tested peptides in existence.
Mechanism of action
A thymic peptide that tunes the immune system, strengthening antiviral T cell responses while also calming overactivity. The most clinically tested peptide in this library.
Also studied
Strengthens Th1 antiviral T cell responses via TLR2/TLR9 on dendritic cells, the basis for its hepatitis B and immune adjunct use.
See related compoundsAlso drives IDO mediated regulatory T cell tolerance, which is why it's studied in both immune deficient and overactive states.
See related compoundsApproved in 35+ countries for chronic hepatitis B/C; backed by 30+ trials and post marketing surveillance of over 600,000 patients.
See related compoundsApplications
Antiviral immune adjunct
Approved in 35+ countries
Adjunct therapy
30+ trials, >11,000 subjects
Immune modulation
Mixed; TESTS trial
Bars indicate how far the evidence has progressed (in vitro to animal to human), not the size of any effect.
Compound data
Literature
Chan HL, Tang JL, Tam W, Sung JJ
Key finding
Pooled across 5 RCTs (353 patients), thymosin roughly doubled the sustained virological response vs control (OR 2.67) at 12 months post treatment.
Full profile
One of the most clinically tested peptides in existence, >30 trials, >11,000 subjects, post marketing surveillance of >600,000 patients; approved in 35+ countries for chronic hepatitis B/C and as an immune adjunct. Hepatitis B data is strongest. Sepsis data is mixed (the large 2025 TESTS trial is the strongest controlled evidence). Anti aging/general immune support use has no RCT.
Among the cleanest safety profiles of any peptide, a 2024 review found it safe and well tolerated across all indications, with no significant treatment related adverse events at therapeutic doses.
Caution in immunosuppression for organ transplant (immune activation) and in autoimmune disease.
Never FDA approved despite global use. Category 2 (Sept 2023); nomination withdrawn Sept 2024; PCAC voted against 503A inclusion (Dec 2024) despite arguably the strongest human evidence on the list. WADA: S0/related.
Subcutaneous; standard 1.6 mg twice weekly.
Source: Fnx Performance Peptide Research Database, a synthesis of the scientific and regulatory literature, not medical advice. Anyone considering these compounds should consult a qualified physician.
For Research Use Only. Not for human or animal consumption. These statements have not been evaluated by the FDA. Products are not intended to diagnose, treat, cure, or prevent any disease.
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