Thymosin Alpha-1 (5 mg Vial)

Thymosin Alpha-1 Dosage Chart

Thymosin Alpha-1 is dosed at 300 mcg–500 mcg daily via subcutaneous injection in educational protocols. A 5 mg vial reconstituted with bacteriostatic water yields about 1.67 mg/mL. This information is for research and educational use only.

Thymosin Alpha-1 (Tα1) is a 28–amino acid peptide originally isolated from the thymus gland, recognized for its broad immunomodulatory properties. It has been investigated as an immune enhancer in chronic viral infections (hepatitis B/C, HIV/AIDS) and critical illness (sepsis, COVID-19). This educational protocol presents a once‑daily subcutaneous approach using a practical dilution for clear insulin‑syringe measurements.

Research context: For evidence on mechanisms, human and preclinical research, limitations, and safety.

Educational guide for reconstitution and daily dosing

Standard / Gradual Approach (3 mL = ~1.67 mg/mL)

Route: Subcutaneous injection | Frequency: Once daily

WeekDaily Dose (mcg)Units (per injection) (mL)
Week 1300 mcg (0.3 mg)18 units (0.18 mL)
Weeks 2–8500 mcg (0.5 mg)30 units (0.30 mL)

Frequency: Inject once daily subcutaneously. This 8‑week protocol begins at 300 mcg to assess tolerance, then increases to a maintenance dose of 500 mcg daily from Week 2 onward. The 500 mcg daily dose yields ~3.5 mg/week, consistent with clinical dosing ranges. Treatment durations of 8–16 weeks are commonly reported in literature.

Reconstitution Steps

Important: This guide is for educational purposes only and is not medical advice. For research use only. Not for human consumption.

Concise summary of the once-daily regimen.

Suggested daily titration approach.

Proper storage preserves peptide quality.

Practical considerations for consistency and safety.

Thymosin Alpha-1 is a naturally occurring thymic peptide that modulates immune function through multiple pathways. It enhances the maturation and differentiation of T‑cells, augments dendritic cell function, and promotes the production of key cytokines including interferon‑α and interleukin‑2. Clinical studies have demonstrated Tα1’s ability to enhance immune responses in immunocompromised individuals, including those with chronic hepatitis B and C infections. Meta-analyses have also shown benefit in reducing mortality in moderate-to-critical COVID-19 patients.

Observations from preclinical and clinical literature.

Complementary strategies for best outcomes.

General subcutaneous guidance from clinical best‑practice resources

This content is for educational purposes only and is not medical advice.

Explore related research dosage protocols and background reading for BPC-157 + TB-500.

World Journal of Virology

— Dominari et al. (2020): Comprehensive review of Thymosin Alpha-1 mechanisms, dosing (0.8–6.4 mg SC), and clinical applications

Molecules (MDPI)

— Tao et al. (2023): Thymosin Alpha-1 in viral diseases—mechanisms and therapeutic applications in HBV, HCV, and HIV

Inflammopharmacology

— Soeroto et al. (2023): Meta-analysis of Tα1 in COVID-19; significant mortality reduction in moderate-to-critical patients

Expert Opinion on Biological Therapy

— Thymalfasin (Zadaxin) clinical overview: 1.6 mg SC twice weekly for hepatitis B treatment

Annals of the New York Academy of Sciences

— Thymosin Alpha-1: biological activities, clinical applications, and pharmacokinetics review

Clinical Immunology

— Mechanisms of thymosin alpha-1 immunomodulation: T-cell maturation and cytokine production

FDA Peptide Advisory Committee (2024)

— Safety data: Tα1 doses up to 16 mg SC for 12 months showed no significant toxicity

Hospital Pharmacy

— Jordan et al. (2021): Small-volume injection accuracy; recommends ≥20% syringe capacity for precision

CDC

— Vaccine administration: subcutaneous route (angle/site; no aspiration required)

Johns Hopkins Arthritis Center

— How to give a subcutaneous injection: site selection, rotation, and technique

NCBI Bookshelf

— Best practices for injection: asepsis, preparation, site rotation, and administration