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Clinical Trial Summary

The second-line treatment for patients who have progressed after first-line immune checkpoint inhibitor therapy, is chemotherapy based on docetaxel and other drugs. The treatment effect is limited. The median survival time of them are 6 months. So there is a huge unmet medical need. This study is a Prospective, Single-arm, Phase II Clinical Trial to Evaluate the Efficacy and Safety of Tafolecimab and Sintilimab Combined With Chemotherapy in Patients With Advanced or Metastatic Driver Gene-negative Non-small Cell Lung Cancer After Failure of First-line Immunotherapy. 30 patients will be enrolled. The main endpoint is PFS,and the secondary endpoint are OS,DCR,DOR,ORR, and so on.


Clinical Trial Description

This is a Prospective, Single-arm, Phase II Clinical Trial to Evaluate the Efficacy and Safety of Tafolecimab and Sintilimab Combined With Chemotherapy in Patients With Advanced or Metastatic Driver Gene-negative Non-small Cell Lung Cancer After Failure of First-line Immunotherapy. 30 patients will be enrolled. These patients will be treated with chemotherapy combined with sintilimab and Tafolecimab. The main endpoint is PFS,and the secondary endpoint are OS,DCR,DOR,ORR, and so on. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06421298
Study type Interventional
Source Beijing Chest Hospital, Capital Medical University
Contact Jinghui Wang
Phone 13683128239
Email jinghuiwang2006@163.com
Status Recruiting
Phase Phase 2
Start date May 17, 2024
Completion date May 30, 2027

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