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Clinical Trial Summary

The purpose of this study is to assess the efficacy and safety of Camrelizumab plus chemotherapy in the treatment of adult participants with medically inoperable Stage I or IIA non-small cell lung cancer (NSCLC).


Clinical Trial Description

This trial will evaluate the safety and efficacy of camrelizumab in combination with chemotherapy, followed by camrelizumab alone after 4-6 cycles of combination in participants with medically inoperable stage I or IIA non-small cell lung cancer (NSCLC). The primary objective of this pilot study is to determine the Camrelizumab plus chemotherapy improves progression-free survival (PFS) . All the efficacy and safety are assessed by investigator : 1) response rate (ORR), 2) disease control rate (DCR); 3) overall survival (OS), 4) PFS rate of 1-year, 2-year, and 5-year; and 5) OS rate of 1-year, 2-year, and 5-year. Explore objective is potential biomarker associated with efficacy. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04530227
Study type Interventional
Source Tianjin Medical University Cancer Institute and Hospital
Contact Changli Wang, PhD
Phone 86-22-23340123
Email wangchangli@medmail.com.cn
Status Recruiting
Phase Phase 2
Start date September 25, 2020
Completion date December 31, 2025

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