drugset / Trial / NCT06421298

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.

NCT06421298

Phase 2 Recruiting 30 enrolled Jinghui Wang
NaSingle-groupOpen-labelTreatment

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.

Timeline

Start
2024-05-17
Primary completion
2027-05-30
Completion
2027-05-30

Drugs

EvaluationDrugModalityDoseRoute
Subject Docetaxel Small molecule 75 mg/m2
Subject Gemcitabine Small molecule 1250 mg/m2
Subject Paclitaxel Small molecule 130 mg/m2
Subject Sintilimab Monoclonal antibody 200 mg
Subject Tafolecimab Monoclonal antibody 450 mg

Indications