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Thymosin-alpha-1

Thymalfasin, Zadaxin, Thymosin α1

Quick Stats
Studies 759
Trials 63
Recruiting PHASE3 INTERVENTIONAL NCT05086614

Thymosin-alpha 1 for Adjuvant Treatment After Radical Resection of High-risk Stage II and III Colorectal Cancer

View on ClinicalTrials.gov Updated Dec 15, 2025

Brief Summary

For high-risk stage II and stage III colorectal cancer, even after radical resection and postoperative adjuvant chemo/radiotherapy, 30-40% of patients will still have recurrence and metastasis. Thymosin-alpha 1 is believed to improve immunity and may help promote tumor immunity to reduce the incidence of recurrence and metastasis. This study hopes to verify the effecacy and safety of thymosin-alpha 1 for adjuvant treatment of high-risk stage II and stage III colorectal cancer after radical resection.

Detailed Description

Patients with pathological high-risk stage II and stage III colorectal cancer after radical resection were randomly allocated to receive thymosin-alpha 1 twice a week for 6 months (experimental group) or not (control group) in a 1:1 ratio. At the same time, all patients will receive chemo/radiotherapy according to the Chinese Standards for Diagnosis and Treatment of Colorectal Cancer. The primary endpoint is 3-year DFS rate.

Interventions

Name: Thymosin Alpha1
Type: DRUG
Description: Receive thymosin-alpha 1 1.6mg with subcutaneous injection, twice a week, for 6 months after radical resection.

Primary Outcomes

Measure: 3-year disease-free survival rate
TimeFrame: 3 years
Description: percentage of patients who have no recurrence or metastases or death at 3 years after surgery.

Trial Information

NCT ID

NCT05086614

Status

Recruiting

Study Type

INTERVENTIONAL

Phases

PHASE3

Sponsor

Fudan University

Last Updated

December 15, 2025