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Clinical Trial Summary

This study is a open-lable, , single center, phase II clinical study. Target population is patients with locally resectable osteosarcoma. Study objective is to compare the efficacy and safety of camrelizumab in combination with adriamycin, cisplatin, ifosfamide and methotrexate in study population in China. Camrelizumab is a humanized anti-PD1 IgG4 monoclonal antibody.


Clinical Trial Description

In this study, eligible subject will be enrolled into study arm to accept study treatment. Treatment cycles of chemotherapy will be at most 9 cycles which will be decided by investigators. The percentage of the patient with tumor cell necrosis rate >90% determined by the Independent Review Committee (IRC) will be the primary outcome measures. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04294511
Study type Interventional
Source Sun Yat-sen University
Contact Jin WANG, MD
Phone 020-87343910
Email wangjinr@sysucc.org.cn
Status Recruiting
Phase Phase 2
Start date December 26, 2019
Completion date September 16, 2023

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