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Meplazumab treats COVID-19 pneumonia: an open-labelled, concurrent controlled add-on clinical trial
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.
Affiliation
  • Huijie Bian; National Translational Science Center for Molecular Medicine & Department of Cell Biology, Fourth Military Medical University
  • Zhao-Hui Zheng; Xijing Hospital, Fourth Military Medical University
  • Ding Wei; National Translational Science Center for Molecular Medicine & Department of Cell Biology, Fourth Military Medical University
  • Zheng Zhang; National Translational Science Center for Molecular Medicine & Department of Cell Biology, Fourth Military Medical University
  • Wen-Zhen Kang; Tangdu Hospital, Fourth Military Medical University
  • Chun-Qiu Hao; Tangdu Hospital, Fourth Military Medical University
  • Ke Dong; Tangdu Hospital, Fourth Military Medical University
  • Wen Kang; Tangdu Hospital, Fourth Military Medical University
  • Jie-Lai Xia; College of Military Preventive Medicine, Fourth Military Medical University
  • Jin-Lin Miao; National Translational Science Center for Molecular Medicine & Department of Cell Biology, Fourth Military Medical University
  • Rong-Hua Xie; Xijing Hospital, Fourth Military Medical University
  • Bin Wang; National Translational Science Center for Molecular Medicine & Department of Cell Biology, Fourth Military Medical University
  • Xiu-Xuan Sun; National Translational Science Center for Molecular Medicine & Department of Cell Biology, Fourth Military Medical University
  • Xiang-Min Yang; National Translational Science Center for Molecular Medicine & Department of Cell Biology, Fourth Military Medical University
  • Peng Lin; National Translational Science Center for Molecular Medicine & Department of Cell Biology, Fourth Military Medical University
  • Jie-Jie Geng; National Translational Science Center for Molecular Medicine & Department of Cell Biology, Fourth Military Medical University
  • Ke Wang; National Translational Science Center for Molecular Medicine & Department of Cell Biology, Fourth Military Medical University
  • Hong-Yong Cui; National Translational Science Center for Molecular Medicine & Department of Cell Biology, Fourth Military Medical University
  • Kui Zhang; Xijing Hospital, Fourth Military Medical University
  • Xiao-Chun Chen; Jiangsu Pacific Meinuoke Biopharmceuticals Co. Ltd.
  • Hao Tang; Jiangsu Pacific Meinuoke Biopharmceuticals Co. Ltd.
  • Hong Du; Tangdu Hospital, Fourth Military Medical University
  • Na Yao; Tangdu Hospital, Fourth Military Medical University
  • Shuang-Shuang Liu; Jiangsu Pacific Meinuoke Biopharmceuticals Co. Ltd.
  • Lin-Na Liu; Tangdu Hospital, Fourth Military Medical University
  • Zhe Zhang; Tangdu Hospital, Fourth Military Medical University
  • Zhao-Wei Gao; Tangdu Hospital, Fourth Military Medical University
  • Gang Nan; National Translational Science Center for Molecular Medicine & Department of Cell Biology, Fourth Military Medical University
  • Qing-Yi Wang; Fourth Military Medical University
  • Jian-Qi Lian; Tangdu Hospital, Fourth Military Medical University
  • Zhi-Nan Chen; National Translational Science Center for Molecular Medicine & Department of Cell Biology, Fourth Military Medical University
  • Ping Zhu; Xijing Hospital, Fourth Military Medical University
Preprint in English | medRxiv | ID: ppmedrxiv-20040691
ABSTRACT
BackgroundSARS-CoV-2 is a novel human coronavirus, there is no specific antiviral drugs. It has been proved that host-cell-expressed CD147 could bind spike protein of SARS-CoV-2 and involve in host cell invasion. Antibody against CD147 could block the infection of SARS-CoV-2. We aimed to assess the efficacy and safety of meplazumab, a humanized anti-CD147 antibody, as add-on therapy in patients with COVID-19 pneumonia. MethodsAll patients received recommended strategy from Diagnosis and Treatment for 2019 Novel Coronavirus Diseases released by National Health Commission of China. Eligible patients were add-on administered 10 mg meplazumab intravenously at days 1, 2, and 5. Patients hospitalized in the same period were observed as concurrent control. The endpoints include virological clearance rate, case severity, chest radiographic, and laboratory test. This trial was approved by the Ethics Committee of Institution at the Tangdu hospital, and registered with ClinicalTrials.gov, NCT 04275245. Findings17 patients were enrolled and assigned to meplazumab group between Feb 3, 2020 and Feb 10, 2020. 11 hospitalized patients served as concurrent control. Baseline characteristics were generally balanced across two groups. Compared to control group, meplazumab treatment significantly improved the discharged (p=0.006) and case severity (p=0.021) in critical and severe patients. The time to virus negative in meplazumab group was reduced than that in control group (median 3, 95%CI[1.5-4.5] vs. 13, [6.5-19.5]; p=0.014, HR=0.37, 95%CI[0.155-0.833]). The percentages of patients recovered to the normal lymphocyte count and CRP concentration were also increased remarkably and rapidly in meplazumab group. No adverse effect was found in meplazumab-treated patients. InterpretationMeplazumab efficiently improved the recovery of patients with SARS-CoV-2 pneumonia with a favorable safety profile. Our results support to carry out a large-scale investigation of meplazumab as a treatment for COVID-19 pneumonia. FundingNational Science and Technology Major Project.
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Full text: Available Collection: Preprints Database: medRxiv Type of study: Experimental_studies / Observational study / Prognostic study / Rct Language: English Year: 2020 Document type: Preprint
Full text: Available Collection: Preprints Database: medRxiv Type of study: Experimental_studies / Observational study / Prognostic study / Rct Language: English Year: 2020 Document type: Preprint
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