4.5 Review

Therapeutic Potential of Nitazoxanide: An Appropriate Choice for Repurposing versus SARS-CoV-2?

Journal

ACS INFECTIOUS DISEASES
Volume 7, Issue 6, Pages 1317-1331

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acsinfecdis.0c00478

Keywords

COVID-19; SARS-CoV-2; coronavirus; antiviral; pharmacokinetics; nitazoxanide; tizoxanide

Funding

  1. Romark Global Pharma LCC
  2. Medical Research Council [MR/S00467X/1]
  3. Unitaid (LONGEVITY)
  4. EPSRC [EP/R024804/1]
  5. EPSRC [EP/R024804/1] Funding Source: UKRI
  6. MRC [MR/N023005/1, MR/S00467X/1] Funding Source: UKRI

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The rapidly spreading COVID-19 pandemic, the most severe global health crisis since 1918, lacks effective drug treatments; nitazoxanide shows promising potential for COVID-19 treatment.
The rapidly growing COVID-19 pandemic is the most serious global health crisis since the Spanish flu of 1918. There is currently no proven effective drug treatment or prophylaxis for this coronavirus infection. While developing safe and effective vaccines is one of the key focuses, a number of existing antiviral drugs are being evaluated for their potency and efficiency against SARS-CoV-2 in vitro and in the clinic. Here, we review the significant potential of nitazoxanide (NTZ) as an antiviral agent that can be repurposed as a treatment for COVID-19. Originally, NTZ was developed as an antiparasitic agent especially against Cryptosporidium spp.; it was later shown to possess potent activity against a broad range of both RNA and DNA viruses, including influenza A, hepatitis B and C, and coronaviruses. Recent in vitro assessment of NTZ has confirmed its promising activity against SARS-CoV-2 with an EC50 of 2.12 mu M. Here we examine its drug properties, antiviral activity against different viruses, clinical trials outcomes, and mechanisms of antiviral action from the literature in order to highlight the therapeutic potential for the treatment of COVID-19. Furthermore, in preliminary PK/PD analyses using clinical data reported in the literature, comparison of simulated TIZ (active metabolite of NTZ) exposures at two doses with the in vitro potency of NTZ against SARS-CoV-2 gives further support for drug repurposing with potential in combination chemotherapy approaches. The review concludes with details of second generation thiazolides under development that could lead to improved antiviral therapies for future indications.

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