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Clinical Trial Summary

Currently, there are no standard treatment and relevant exploration for NSCLC patients with NED. The study aims to explore the efficacy and safety of surufatinib combined with tislelizumab in the treatment of NSCLC with NED, in order to provide a new treatment option for NSCLC patients with NED.


Clinical Trial Description

This is a single-arm, open, single-center, prospective and exploratory clinical study. We planned to enroll 29 patients who would receive surufatinib plus tislelizumab until disease progression, intolerance, or withdrawal of consent. The study aims to explore the efficacy and safety of surufatinib combined with tislelizumab in the treatment of NSCLC with NED, in order to provide a new treatment option for NSCLC patients with NED. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06414915
Study type Interventional
Source National Cancer Center, China
Contact Puyuan Xing, Doctorate
Phone +86-10-87787421
Email xingpuyuan@cicams.ac.cn
Status Not yet recruiting
Phase Phase 2
Start date June 1, 2024
Completion date June 1, 2027

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