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Thymosin-alpha-1

Thymalfasin, Zadaxin, Thymosin α1

Quick Stats
Studies 759
Trials 63
Score 2
1996 pubmed

A double-blind, placebo-controlled, pilot trial of thymosin alpha 1 for the treatment of chronic hepatitis C.

Andreone. P P; Cursaro. C C; Gramenzi. A A; Buzzi. A A; Covarelli. M G MG; Di Giammarino. L L; Miniero. R R; Arienti. V V; Bernardi. M M; Gasbarrini. G G

Key Findings

  • No patient cleared HCV‑RNA after treatment.
  • Mean ALT levels did not change significantly in either the thymosin‑alpha‑1 or placebo groups.
  • One treated patient briefly normalized ALT but relapsed after follow‑up; no serious side effects were reported.
  • The regimen was well‑tolerated aside from occasional local injection discomfort.

Practical Outcomes

  • For biohackers considering thymosin‑alpha‑1 for antiviral or liver health purposes, this study suggests it is not effective against chronic hepatitis C and offers no clear benefit for liver enzyme control. The peptide appears safe at the tested dose, but any use should be limited to other proven indications, not hepatitis C treatment.

Summary

In a small Italian trial, giving thymosin‑alpha‑1 twice a week for six months did not clear hepatitis C virus or meaningfully lower liver enzymes, and only caused mild injection‑site discomfort.

Abstract

A randomized, double-blind, placebo-controlled trial was performed to evaluate the efficacy and safety of thymosin alpha 1 (alpha 1) in treating chronic hepatitis C. Nineteen Italian patients with chronic active hepatitis C, proven by biopsy were randomly assigned to receive a six month course of thymosin alpha 1 (900 micrograms/m2 of body surface area twice weekly) or a placebo. All had HCV-RNA in their serum (by PCR), with serum ALT levels more than double the upper limit of the normal range for at least six months before enrollment. After treatment, patients were followed for an additional six months. All patients completed the trial. One patient treated with thymosin alpha 1, but no patient in the placebo group, normalized serum ALT levels by the end of the treatment. This patient, however, relapsed at the sixth month of the follow up. Overall, there were no significant changes in mean serum ALT levels in either group during the treatment or follow-up period. No patient cleared HCV-RNA. No side effects were reported except for local discomfort at the injection sites, reported by some patients treated with thymosin alpha 1. In conclusion, this regimen of thymosin alpha 1 is not effective in the treatment of chronic hepatitis C.

Study Information

Provider

pubmed

Year

1996

DOI

10.1111/j.1600-0676.1996.tb00729.x