Subcutaneous tocilizumab in adults with severe and critical COVID-19: A prospective open-label uncontrolled multicenter trial
[Display omitted] •Excessive inflammation leads to lung damage in complicated COVID-19 patients.•Tocilizumab, an IL-6 inhibitor, was added to the standard treatment in this study.•Comparably low mortality rate (6.98%) was observed in severe patients.•Benefits of tocilizumab were less considerable in...
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Veröffentlicht in: | International immunopharmacology 2020-12, Vol.89 (Pt B), p.107102-107102, Article 107102 |
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Hauptverfasser: | , , , , , , , , , , , , , , , , , , |
Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | [Display omitted]
•Excessive inflammation leads to lung damage in complicated COVID-19 patients.•Tocilizumab, an IL-6 inhibitor, was added to the standard treatment in this study.•Comparably low mortality rate (6.98%) was observed in severe patients.•Benefits of tocilizumab were less considerable in patients with critical disease.•Appropriate timing is important in the administration of tocilizumab for COVID-19.
Potential therapeutic approaches in coronavirus disease 2019 (COVID-19) comprise antiviral and immunomodulatory agents; however, no immunomodulator drug has been approved. This multicenter, prospective, open-label, uncontrolled study aimed to assess the use of subcutaneous tocilizumab in adult patients with severe and critical COVID-19. Tocilizumab was added to the standard care of therapy at a dose of 324 mg ( |
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ISSN: | 1567-5769 1878-1705 |
DOI: | 10.1016/j.intimp.2020.107102 |