研究单位:[1]Sunshine Guojian Pharmaceutical (Shanghai) Co., Ltd.[2]Beijing Luhe Hospital Capital Medical University Beijing, Beijing, China, 101100[3]Sun Yat-Sen University Cancer Hospital Guangzhou, Guangdong, China, 510600[4]The Fourth Hospital of Hebei Medical University Shijiazhuang, Hebei, China, 050010河北医科大学第四医院[5]Affiliated Hospital of Hebei University Baoding, Heibei, China, 071000[6]Zhengzhou Central Hospital Zhengzhou, Henan, China, 450007[7]The First Affiliated Hospita of Zhengzhou University Zhengzhou, Henan, China, 450052[8]Weihai Municipal Hospital Weihai, Shandong, China, 264200[9]Tianjin Medical University Cancer Institute &Hospital Tianjing, Tianjing, China, 300060[10]The Second Affiliated Hospital of Soochow University Suzhou, Zhejiang, China, 215000[11]The 307 Hospital of People's Liberation Army Beijing, Beijing, China, 100071
研究目的:
The purpose of this study is to evaluate the pharmacokinetic of the experimental drug 304 injection compared with rituximab injection in patients with CD20 positive B-cell non-Hodgkin lymphoma who had previously achieved CR/CRu status but had not deteriorated or relapsed. While to assess the safety and efficacy of the experimental drug 304 injection compared with rituximab injection.