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创胜集团 - 全整合型国际化生物制药公司

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学术论文及会议壁报

人源化抗Claudin18.2单克隆抗体TST001联合CAPOX作为局部晚期或转移性胃癌及胃食管连接部癌一线治疗的I/II期临床试验剂量扩展队列研究的中期安全性和疗效数据

13 Sep, 2022

Authors:

Jifang Gong1 , Ning Li2 , Weijian Guo3, Tianshu Liu4 , Hongli Li5 , Jiayi Li 6 , Zhenzhong Xia7 , Chunhua Qian 7 , Jenny Yao 8 , Jianming Wang 8 , Lijuan Zhang 7 , Chuan Qi 7 , Michael Shi 8 , Xu,Li 8 , Caroline Germa 8 , Xueming Qian 7 , Lin Shen 1 ;

1Department of Gastrointestinal Oncology, Peking University Cancer Hospital and Institute, Beijing, China; 2Henan Cancer Hospital, Zhengzhou, China; 3Department of Medical Oncology, Fudan University Shanghai Cancer Center, Shanghai, China; 4Zhongshan Hospital, Fudan University, Shanghai, China; 5Tianjin Medical University Cancer Institute and Hospital, Tianjin, China; 6The First Affiliated Hospital of Xiamen University, Xiamen, China; 7Suzhou Transcenta Therapeutics Co., Ltd; 8Transcenta Therapeutics Inc.

Background:

TST001 is a recombinant humanized antibody that can specifically bind to the  extracellular structure of Claudin18.2 (CLDN18.2) protein and eliminate cancer cells  by antibody-dependent cellular cytotoxicity and complement-dependent  cytotoxicity.  

Pre-clinical studies have shown that TST001 has synergistic effect when used in  combination with chemotherapy.

Conclusions:

TST001 in combination with CAPOX as the first line treatment of patients with G/GEJ  cancer is well tolerated and encouraging anti-tumor activities have been observed.  CLDN18.2 expression thresholds and correlation with efficacy are being further  assessed.

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