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
Hauptverfasser: Malekzadeh, Reza, Abedini, Atefeh, Mohsenpour, Behzad, Sharifipour, Ehsan, Ghasemian, Roya, Javad-Mousavi, Seyed Ali, Khodashahi, Rozita, Darban, Mahboobeh, Kalantari, Saeed, Abdollahi, Nafiseh, Salehi, Mohammad Reza, Rezaei Hosseinabadi, Abbas, Khorvash, Farzin, Valizadeh, Melika, Dastan, Farzaneh, Yousefian, Sahar, Hosseini, Hamed, Anjidani, Nassim, Tabarsi, Payam
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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 (
ISSN:1567-5769
1878-1705
DOI:10.1016/j.intimp.2020.107102