Pre-clinical evaluation of antiviral activity of nitazoxanide against SARS-CoV-2
Jean-Sélim Driouich,
Maxime Cochin,
Franck Touret,
Paul-Rémi Petit,
Magali Gilles,
Grégory Moureau,
Karine Barthélémy,
Caroline Laprie,
Thanaporn Wattanakul,
Palang Chotsiri,
Richard M. Hoglund,
Joel Tarning,
Laurent Fraisse,
Peter Sjö,
Charles E. Mowbray,
Fanny Escudié,
Ivan Scandale,
Eric Chatelain,
Xavier de Lamballerie,
Caroline Solas,
Antoine Nougairède
Affiliations
Jean-Sélim Driouich
Unité des Virus Émergents (UVE: Aix-Marseille University -IRD 190-Inserm 1207), Marseille, France; Corresponding author.
Maxime Cochin
Unité des Virus Émergents (UVE: Aix-Marseille University -IRD 190-Inserm 1207), Marseille, France
Franck Touret
Unité des Virus Émergents (UVE: Aix-Marseille University -IRD 190-Inserm 1207), Marseille, France
Paul-Rémi Petit
Unité des Virus Émergents (UVE: Aix-Marseille University -IRD 190-Inserm 1207), Marseille, France
Magali Gilles
Unité des Virus Émergents (UVE: Aix-Marseille University -IRD 190-Inserm 1207), Marseille, France
Grégory Moureau
Unité des Virus Émergents (UVE: Aix-Marseille University -IRD 190-Inserm 1207), Marseille, France
Karine Barthélémy
Unité des Virus Émergents (UVE: Aix-Marseille University -IRD 190-Inserm 1207), Marseille, France
Caroline Laprie
Laboratoire Vet-Histo, Marseille, France
Thanaporn Wattanakul
Mahidol Oxford Tropical Medicine Research Unit, Faculty of Tropical Medicine, Mahidol University, Bangkok, Thailand
Palang Chotsiri
Mahidol Oxford Tropical Medicine Research Unit, Faculty of Tropical Medicine, Mahidol University, Bangkok, Thailand
Richard M. Hoglund
Mahidol Oxford Tropical Medicine Research Unit, Faculty of Tropical Medicine, Mahidol University, Bangkok, Thailand; Centre for Tropical Medicine and Global Health, Nuffield Department of Clinical Medicine, University of Oxford, Oxford, United Kingdom
Joel Tarning
Mahidol Oxford Tropical Medicine Research Unit, Faculty of Tropical Medicine, Mahidol University, Bangkok, Thailand; Centre for Tropical Medicine and Global Health, Nuffield Department of Clinical Medicine, University of Oxford, Oxford, United Kingdom
Laurent Fraisse
Drugs for Neglected Diseases initiative, Geneva, Switzerland
Peter Sjö
Drugs for Neglected Diseases initiative, Geneva, Switzerland
Charles E. Mowbray
Drugs for Neglected Diseases initiative, Geneva, Switzerland
Fanny Escudié
Drugs for Neglected Diseases initiative, Geneva, Switzerland
Ivan Scandale
Drugs for Neglected Diseases initiative, Geneva, Switzerland
Eric Chatelain
Drugs for Neglected Diseases initiative, Geneva, Switzerland
Xavier de Lamballerie
Unité des Virus Émergents (UVE: Aix-Marseille University -IRD 190-Inserm 1207), Marseille, France
Caroline Solas
Unité des Virus Émergents (UVE: Aix-Marseille University -IRD 190-Inserm 1207), Marseille, France; APHM, Laboratoire de Pharmacocinétique et Toxicologie, Hôpital La Timone, Marseille, France
Antoine Nougairède
Unité des Virus Émergents (UVE: Aix-Marseille University -IRD 190-Inserm 1207), Marseille, France
Summary: 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 tizoxanide 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 santé et de la recherche médicale” through the REACTing (REsearch and ACTion targeting emerging infectious diseases), by REACTING/ANRS MIE under the agreement No. 21180 (‘Activité des molécules antivirales dans le modèle 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 support by the Wellcome Trust Grant ref: 222489/Z/21/Z through the COVID-19 Therapeutics Accelerator”.