4.7 Article

Pre-clinical evaluation of antiviral activity of nitazoxanide against SARS-CoV-2

Journal

EBIOMEDICINE
Volume 82, Issue -, Pages -

Publisher

ELSEVIER
DOI: 10.1016/j.ebiom.2022.104148

Keywords

COVID-19; SARS-CoV-2; Antiviral therapy; Pre-clinical research; Nitazoxanide; Animal model

Funding

  1. Fondation de France
  2. REACTING/ANRS MIE [21180]
  3. European Union [871029]
  4. Wellcome Trust [222489/Z/21/Z]
  5. European Virus Archive Global [EVA 213 GLOBAL]
  6. Wellcome Trust [222489/Z/21/Z] Funding Source: Wellcome Trust

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This study evaluated the preclinical activity of nitazoxanide against SARS-CoV-2. The results showed that nitazoxanide had some inhibitory effects on SARS-CoV-2 in vitro and in models, but the concentrations used in actual treatment were insufficient to affect viral replication in affected organs.
Background To address the emergence of SARS-CoV-2, multiple clinical trials in humans were rapidly started, including those involving an oral treatment by nitazoxanide, despite no or limited pre-clinical evidence of antiviral efficacy. Methods In this work, we present a complete pre-clinical evaluation of the antiviral activity of nitazoxanide against SARS-CoV-2. Findings First, we confirmed the in vitro efficacy of nitazoxanide and tizoxanide (its active metabolite) against SARS-CoV-2. Then, we demonstrated nitazoxanide activity in a reconstructed bronchial human airway epithelium model. In a SARS-CoV-2 virus challenge model in hamsters, oral and intranasal treatment with nitazoxanide failed to impair viral replication in commonly affected organs. We hypothesized that this could be due to insufficient diffusion of the drug into organs of interest. Indeed, our pharmacokinetic study confirmed that concentrations of tizoxa-nide in organs of interest were always below the in vitro EC50. Interpretation These preclinical results suggest, if directly applicable to humans, that the standard formulation and dosage of nitazoxanide is not effective in providing antiviral therapy for Covid-19. Funding This work was supported by the Fondation de France call FLASH COVID-19 , project TAMAC, by Institut national de la sante? et de la recherche me?dicale through the REACTing (REsearch and ACTion targeting emerging infectious diseases), by REACTING/ANRS MIE under the agreement No. 21180 ('Activite? des mole?cules antivirales dans le mod?ele hamster'), by European Virus Archive Global (EVA 213 GLOBAL) funded by the European Union's Horizon 2020 research and innovation program under grant agreement No. 871029 and DNDi under sup-port by the Wellcome Trust Grant ref: 222489/Z/21/Z through the COVID-19 Therapeutics Accelerator . Copyright (C) 2022 The Author(s). Published by Elsevier B.V.

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