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10.1016/j.biopha.2020.110825

http://scihub22266oqcxt.onion/10.1016/j.biopha.2020.110825
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suck abstract from ncbi


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pmid33378989      Biomed+Pharmacother 2021 ; 133 (ä): 110825
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  • Tocilizumab combined with favipiravir in the treatment of COVID-19: A multicenter trial in a small sample size #MMPMID33378989
  • Zhao H; Zhu Q; Zhang C; Li J; Wei M; Qin Y; Chen G; Wang K; Yu J; Wu Z; Chen X; Wang G
  • Biomed Pharmacother 2021[Jan]; 133 (ä): 110825 PMID33378989show ga
  • BACKGROUND: Since December 2019, COVID-19 has spread to almost every corner of the world. In theory, tocilizumab and favipiravir are considered to be reliable drugs for the treatment of COVID-19 with elevated IL-6. We aimed to assess the efficacy and safety of tocilizumab combined with favipiravir in patients with COVID-19. METHODS: This was a multicenter trial in adults with COVID-19. Patients were randomly assigned (3:1:1) to a 14-day combination of favipiravir combined with tocilizumab (combination group), favipiravir, and tocilizumab. The primary outcome was the cumulative lung lesion remission rate (lung CT examination indicated absorption of lung inflammation). RESULTS: Between Feb 2 and March 15, 2020, 26 patients were recruited; 14 were randomly assigned to the combination group, 7 were assigned to the favipiravir group and 5 were assigned to the tocilizumab group. The cumulative lung lesion remission rate at day 14 was significantly higher in combination group as compared with favipiravir group (P = 0.019, HR 2.66 95 % CI [1.08-6.53]). And there was also a significant difference between tocilizumab and favipivavir (P = 0.034, HR 3.16, 95 % CI 0.62-16.10). In addition, there was no significant difference between the combination group and the tocilizumab group (P = 0.575, HR 1.28 95 %CI 0.39-4.23). Furthermore, combined therapy can also significantly relieve clinical symptoms and help blood routine to return to normal. No serious adverse events were reported. CONCLUSION: Tocilizumab combined with or without favipiravir can effectively improve the pulmonary inflammation of COVID-19 patients and inhibit the deterioration of the disease.
  • |*COVID-19 Drug Treatment[MESH]
  • |Adult[MESH]
  • |Aged[MESH]
  • |Aged, 80 and over[MESH]
  • |Amides/administration & dosage/adverse effects/*therapeutic use[MESH]
  • |Antibodies, Monoclonal, Humanized/administration & dosage/adverse effects/*therapeutic use[MESH]
  • |Antiviral Agents/administration & dosage/adverse effects/*therapeutic use[MESH]
  • |COVID-19/diagnostic imaging/pathology/therapy[MESH]
  • |Drug Therapy, Combination[MESH]
  • |Female[MESH]
  • |Humans[MESH]
  • |Interleukin-6/blood[MESH]
  • |Kaplan-Meier Estimate[MESH]
  • |Lung/diagnostic imaging/pathology[MESH]
  • |Male[MESH]
  • |Middle Aged[MESH]
  • |Models, Immunological[MESH]
  • |Pyrazines/administration & dosage/adverse effects/*therapeutic use[MESH]
  • |Receptors, Interleukin-6/antagonists & inhibitors[MESH]
  • |Respiration, Artificial/statistics & numerical data[MESH]
  • |SARS-CoV-2/*drug effects[MESH]
  • |Sample Size[MESH]


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