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      Ruxolitinib in treatment of severe coronavirus disease 2019 (COVID-19): A multicenter, single-blind, randomized controlled trial

      research-article
      , M.D., Ph.D. 1 , 2 , , , M.D., Ph.D. 1 , 2 , , , M.D 3 , , , M.D 4 , , , M.D, Ph.D. 1 , 2 , , Ph.D 1 , 2 , , M.D, Ph.D. 1 , 2 , , M.D., Ph.D. 1 , 2 , , M.D., Ph.D. 1 , 2 , , M.D., Ph.D. 1 , 2 , , M.D., Ph.D. 1 , 2 , , , M.D., Ph.D. 1 , 2 , , M.D., Ph.D. 1 , 2 , , M.D., Ph.D. 1 , 2 , , M.D., Ph.D. 5 , , M.D., Ph.D. 4 , , M.D 3 , , M.D., Ph.D. 5 , , Ph.D 6 , # , , M.D., Ph.D. 7 , # , , M.D., Ph.D. 1 , 2 , ∗∗ , # ,
      The Journal of Allergy and Clinical Immunology
      Published by Elsevier Inc. on behalf of the American Academy of Allergy, Asthma & Immunology.
      Ruxolitinib, COVID-19, cytokine storm, efficacy, safety, randomized controlled trial, COVID-19, Coronavirus disease 2019, SARS-CoV-2, Severe acute respiratory syndrome coronavirus 2, SoC, Standard-of-care, IL-6, Interleukin-6, RCT, Randomized controlled trial, JAK, Janus-associated kinase, IQR, Interquartile range, CT, Computed tomography

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          Abstract

          Background

          Accumulating evidence proposed JAK inhibitors as therapeutic targets warranting rapid investigation.

          Objective

          This study evaluated the efficacy and safety of ruxolitinib, a Janus-associated kinase (JAK1/2) inhibitor, for COVID-19.

          Methods

          We conducted a prospective, multicenter, single-blind, randomized controlled phase II trial involving patients with severe COVID-19.

          Results

          Forty-three patients were randomly assigned (1:1) to receive ruxolitinib plus SoC treatment (22 patients) or placebo based on SoC treatment (21 patients). After exclusion of 2 patients (1 ineligible, 1 consent withdrawn) from the ruxolitinib group, 20 patients in intervention group and 21 patients in control group were included in the study. Treatment with ruxolitinib plus SoC was not associated with significantly accelerated clinical improvement in severe patients with COVID-19, although ruxolitinib recipients had a numerically faster clinical improvement. Eighteen (90%) patients from the ruxolitinib group showed CT improvement at D 14 compared with 13 (61.9%) patients from the control group ( P = 0.0495). Three patients in the control group died of respiratory failure, with 14.3% overall mortality at D 28; no patients died in the ruxolitinib group. Ruxolitinib was well tolerated with low toxicities and no new safety signals. Levels of 7 cytokines were significantly decreased in the ruxolitinib group in comparison to the control group.

          Conclusions

          Although no statistical difference was observed, ruxolitinib recipients had a numerically faster clinical improvement. Significant chest CT improvement, a faster recovery from lymphopenia and favorable side-effect profile in ruxolitinib group were encouraging and informative to future trials to test efficacy of ruxolitinib in a larger population.

          This trial is registered at www.chictr.org.cn as ChiCTR-OPN-2000029580.

          Abstract

          The results of the present study showed that ruxolitinib plus SoC was well tolerated in the treatment of severe COVID-19. It significantly mitigated exuberant cytokine storm featured in severe COVID-19, with significant chest CT improvement.

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          Author and article information

          Contributors
          Journal
          J Allergy Clin Immunol
          J. Allergy Clin. Immunol
          The Journal of Allergy and Clinical Immunology
          Published by Elsevier Inc. on behalf of the American Academy of Allergy, Asthma & Immunology.
          0091-6749
          1097-6825
          26 May 2020
          26 May 2020
          Affiliations
          [1 ]Department of Hematology, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, No. 1095 Jiefang Avenue, Wuhan, Hubei 430030, China;
          [2 ]Clincal Trial and Research Center of Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, Hubei 430030, China;
          [3 ]Department of Hematology, Wuhan No. 1 Hospital, No. 215 Zhongshan Ave., Wuhan, 430022, China;
          [4 ]Hematology Department of The Third Xiangya Hospital Central South University, 410013, Changsha, China;
          [5 ]Department of Respiratory and Critical Care Medicine, Key Laboratory of Pulmonary Diseases of Health Ministry, Key Cite of National Clinical Research Center for Respiratory Disease, Tongji Hospital, Tongji Medical College Huazhong University of Science and Technology, No. 1095 Jie Fang Avenue, 430030, Wuhan, China;
          [6 ]Divisions of Pathology and Experimental Hematology and Cancer Biology, Cincinnati Children's Hospital Medical Center, 3333 Burnet Avenue, Room S7.224, Cincinnati, Ohio, USA
          [7 ]Department of Neurology, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, No. 1095 Jiefang Avenue, Wuhan 430030, Hubei, China
          Author notes
          [∗∗ ]Correspondence: Dr. Jianfeng Zhou, Department of Hematology, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, 1095 Jiefang Avenue, Wuhan, Hubei 430030, China; or Tel: +86-27- 83665506 ; Fax: +86-27-83662680. jfzhou@ 123456tjh.tjmu.edu.cn
          [∗]

          These authors contributed equally to this work.

          [#]

          Joint corresponding authors.

          Article
          S0091-6749(20)30738-7
          10.1016/j.jaci.2020.05.019
          7250105
          32470486
          e1735270-7e1e-4391-a45a-9243d56aeff2
          © 2020 Published by Elsevier Inc. on behalf of the American Academy of Allergy, Asthma & Immunology.

          Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.

          History
          : 24 April 2020
          : 13 May 2020
          : 19 May 2020
          Categories
          Article

          Immunology
          ruxolitinib,covid-19,cytokine storm,efficacy,safety,randomized controlled trial,covid-19, coronavirus disease 2019,sars-cov-2, severe acute respiratory syndrome coronavirus 2,soc, standard-of-care,il-6, interleukin-6,rct, randomized controlled trial,jak, janus-associated kinase,iqr, interquartile range,ct, computed tomography

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