Author: Huijie Bian; Zhao-Hui Zheng; Ding Wei; Zheng Zhang; Wen-Zhen Kang; Chun-Qiu Hao; Ke Dong; Wen Kang; Jie-Lai Xia; Jin-Lin Miao; Rong-Hua Xie; Bin Wang; Xiu-Xuan Sun; Xiang-Min Yang; Peng Lin; Jie-Jie Geng; Ke Wang; Hong-Yong Cui; Kui Zhang; Xiao-Chun Chen; Hao Tang; Hong Du; Na Yao; Shuang-Shuang Liu; Lin-Na Liu; Zhe Zhang; Zhao-Wei Gao; Gang Nan; Qing-Yi Wang; Jian-Qi Lian; Zhi-Nan Chen; Ping Zhu
Title: Meplazumab treats COVID-19 pneumonia: an open-labelled, concurrent controlled add-on clinical trial Document date: 2020_3_24
ID: 6g34qwer_17
Snippet: The primary study endpoint was the virological clearance (i.e. negative conservation rate and time to negative) using qRT-PCR in nasopharyngeal swabs samples. Secondary efficacy endpoints were assessment of time to recovery of vital sign (including body temperature, respiratory rate, and SPO2), chest radiographic improvement, rate of PaO2/FiO2 recovery, time (days) to discharge, and inflammation recovery (percentage of patient with normal CRP con.....
Document: The primary study endpoint was the virological clearance (i.e. negative conservation rate and time to negative) using qRT-PCR in nasopharyngeal swabs samples. Secondary efficacy endpoints were assessment of time to recovery of vital sign (including body temperature, respiratory rate, and SPO2), chest radiographic improvement, rate of PaO2/FiO2 recovery, time (days) to discharge, and inflammation recovery (percentage of patient with normal CRP concentration).
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