Menu
Peptide Database
Results
No peptides found
Featured

Use search to browse all 100+ peptides

Thymosin-alpha-1

Thymalfasin, Zadaxin, Thymosin α1

Quick Stats
Studies 759
Trials 63
Unknown PHASE2 INTERVENTIONAL NCT02976740

SBRT Combination With rhGM-CSF and Tα1 for Stage IV NSCLC Patients Who Failed in Second-line Chemotherapy

View on ClinicalTrials.gov Updated Dec 15, 2025

Brief Summary

The purpose of this study is to determine whether stereotactic body radiotherapy (SBRT) combined with recombined human granulocyte-macrophage colony stimulating factor(rhGM-CSF) and Thymosin Alpha 1 is safe, effective in the treatment of stage IV NSCLC patients who failed in second-line chemotherapy.

Detailed Description

Metastasis lesion of stage IV NSCLC will be treated with a SBRT of 50Gy/4-10F from day 1 to day 14 in one cycle. Subcutaneous injection of human recombined granulocyte-macrophage colony stimulating factor (125ug/m² per day) will be executed from day 1 to day 14 in this cycle. Another metastasis lesion will be treated likewise concurrently with rhGM-CSF in a consecutive cycle.Thymosin Alpha 1(1.6mg Biw) will be Subcutaneous injection from the fist week to the 12th weeks, Efficacy evaluation, especially abscopal effect evaluation, will be conducted at the end of therapy and every month after that. Adverse events will be recorded according to NCI-CTC version 4.03.

Interventions

Name: SBRT
Type: RADIATION
Description: Stereotactic body radiotherapy A type of radiation therapy to the Metastasis lesion
Name: Immunological Agent
Type: DRUG
Description: Subcutaneous injection of human recombined granulocyte-macrophage colony stimulating factor (125ug/m² per day) will be executed from day 1 to day 14 in this cycle. Another metastasis lesion will be treated likewise concurrently with rhGM-CSF in a consecutive cycle.
Name: Immunological Factors
Type: DRUG
Description: Thymosin Alpha 1(1.6mg Biw)will be executed from the fist Week to the 12th Weeks.

Primary Outcomes

Measure: abscopal effect rate
TimeFrame: at the time point of 4 weeks after completion of the combined treatment
Description:

Trial Information

NCT ID

NCT02976740

Status

Unknown

Study Type

INTERVENTIONAL

Phases

PHASE2

Sponsor

The First Affiliated Hospital of Xiamen University

Last Updated

December 15, 2025