ID: thymosin_alpha1
Aliases: Ta1, Zadaxin, THYMOSIN ALPHA-1
Type: compound
Route/form: subcutaneous injection in labelled/regional use
Status: approved_in_some_countries
Evidence level: human RCT
Best data tier: human controlled/review; exact-use indirect
Support scope: human
Source types: human_rct, human_rct_negative
Linked sources: 3
Broad outcomes: Gut / immune / inflammation
Reading note: These are curation notes anchored to linked sources, not a clinical recommendation or protocol.
Targets / mechanism
- immune modulation
- T-cell function
Optimization domains
- immune
- infection
- oncology adjunct
Research basis
- Human randomized trials exist in serious immune/infectious-disease contexts, with immune-parameter and clinical-endpoint signals.
- Useful as a contrast against purely preclinical peptides.
Limits, risks, and missing evidence
- Indications and regulatory status vary by country, and disease-context trials do not validate generic immune-optimization use.
- A large 2025 phase 3 sepsis RCT found no clear evidence of reduced 28-day all-cause mortality in adults with sepsis.
- Wellness-stack use often ignores immune phenotype and endpoint selection.
Risk flags
- immune modulation
- medical supervision
- disease context human data
Linked papers, labels, and reviews
- Thymosin alpha 1 is associated with improved cellular immunity and reduced infection rate in severe acute pancreatitis patients
human_rct / pubmed_thymosin_alpha1_pancreatitis_rct_2010
Double-blind randomized pilot trial with immune parameters and infection outcomes. - The efficacy of thymosin alpha 1 for severe sepsis (ETASS): a multicenter randomized controlled trial
human_rct / pmc_thymosin_alpha1_sepsis_etass_2014
Multicenter severe sepsis RCT; useful for immune-modulation evidence and limitations. - The efficacy and safety of thymosin alpha 1 for sepsis (TESTS): multicentre, double blinded, randomised, placebo controlled, phase 3 trial
human_rct_negative / bmj_thymosin_alpha1_tests_sepsis_2025
Large phase 3 sepsis RCT; found no clear evidence that thymosin alpha 1 decreased 28-day all-cause mortality in adults with sepsis.