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Clinical Trial Summary

This prospective phase II randomized study is to determine the impact of thymosin alpha-1 on the concurrent chemoradiotherpay followed by immunotherapy consolidation in patients with locally advanced NSCLC by assessing the survival outcomes, treatment responses and toxicities.


Clinical Trial Description

This prospective phase II randomized study is to determine the impact of thymosin alpha-1 on the concurrent chemoradiotherpay followed by immunotherapy consolidation in patients with locally advanced NSCLC by assessing the survival outcomes, treatment responses and toxicities. Patients with locally advanced NSCLC who will receive concurrent radiochemotherapy followed by immunotherapy consolidation will be randomly divided into two groups (concurrent Tα1 treatment group and control group [in which Tα1 will not be used]), and the overall survivals, progression-free survivals (PFS), completion rate of immunotherapy consolidation, toxicities/adverse effects, and peripheral blood immune biomarkers will be compared between these two groups. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06139419
Study type Interventional
Source Sun Yat-sen University
Contact Bo Qiu, Professor
Phone +86-020-87343031
Email qiubo@sysucc.org.cn
Status Recruiting
Phase Phase 2
Start date July 25, 2023
Completion date August 2026

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