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Home > Research and development > Portfolio

Pandemic Preparedness 

Pre-clinical support

objective

Identify and validate potential drug candidates from known antivirals and build translational understanding to support prediction of efficacy based on data from in vitro and in vivo pre-clinical models

project start
2020
project status
Completed

last phase of drug development

Discovery project phase
Drug Discovery
Translation project phase
Translational research
clinical trials icon
Clinical trials
Treatment Access
Registration & access

updated 16 Feb 2023

DNDi is supporting the ANTICOV clinical trial by identifying and validating repurposed drug candidates, beginning with the in vitro and in vivo experimental work needed to provide supporting pre-clinical evidence. We are focusing mainly on compounds that have a direct-acting antiviral profile and on combinations of antivirals and anti-inflammatories.

COVID-19 has several phases – from an initial viral stage to a later inflammatory stage – which contributes to a lack of consensus understanding of the translational value of in vitro and in vivo experimental models. To help overcome this knowledge gap, our discovery team is also working to expand the translational understanding of how data generated in pre-clinical in vitro and in vivo models can help to predict the future efficacy of investigational drug candidates in patients.

Project updates

2022

Translational studies supporting the selection of new ANTICOV trial treatment arms continued with 19 compounds with different modes of action thoroughly investigated in in vitro and in vivo SARS-CoV2 infection models. In addition to repurposed drugs, several experimental or recently approved drugs were investigated. Of the compounds assessed, including MPro inhibitors (nirmatrelvir and ensitrelvir) and RdRp inhibitors (favipiravir and molnupiravir), very few showed a significant antiviral effect against SARS-CoV2 infection in in vivo models. Key data and conclusions from the translational studies supporting the selection of ANTICOV arms have been summarized in public disclosures and peer-reviewed publications, including a key publication summarizing data for all compounds included in the translational study. In parallel, initial data from the fluoxetine arm of the trial – showing compound efficacy – are being confirmed by additional studies at the University of Toulouse and the University of Liverpool. 

2021

DNDi continued to offer pre-clinical support for the selection of new treatment arms in the ANTICOV trial. Additional compounds were assessed based on clinical and pre-clinical literature, including the new RdRp inhibitors (molnupiravir, AT-527) and MPro inhibitors (PF-07321332), with clinical data now being published. This project is both providing support to ANTICOV with pre-clinical evidence for the selection of clinical trial arms, as well as helping to define a clear path forward from in vitro data to in vivo efficacy assessment based on clear pharmacokinetic data and modelling. 

2020

In vivo experiments to obtain pre-clinical data on several known antivirals (ritonavir-boosted atazanavir, nitazoxanide, favipiravir, sofosbuvir, and daclatasvir) were started in November 2020 in collaboration with the Katholieke Universiteit Leuven, the Unité de Virus émergents at the Université d’Aix-Marseille, and the University of Liverpool. At least three more potential treatments will be investigated in 2021.

News & resources

  • 12 August 2022 – Need for a standardized translational drug development platform: Lessons learned from the repurposing of drugs for COVID-19, Microorganisms

Partners

  • Aix-Marseille Université, Unité de Virus émergents, France
  • Centre National de Recherche Scientifique (CNRS), France
  • Institut Pasteur Korea (IPK), Republic of Korea
  • Katholieke Universiteit Leuven, Belgium
  • Mahidol Oxford Tropical Medicine Research Unit (MORU), Thailand
  • University of Liverpool, UK
  • University of Toulouse, France
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  • Aix-Marseille Université, Unité de Virus émergents
  • ,France
  • Centre National de Recherche Scientifique (CNRS)
  • ,France
  • Institut Pasteur Korea (IPK)
  • ,Republic of Korea
  • Katholieke Universiteit Leuven
  • ,Belgium
  • Mahidol Oxford Tropical Medicine Research Unit (MORU)
  • ,Thailand
  • University of Liverpool
  • ,UK
  • University of Toulouse
  • ,France
  • University of Liverpool, UK
  • Katholieke Universiteit Leuven, Belgium
  • Aix-Marseille Université, Unité de Virus émergents, France
  • Institut Pasteur Korea (IPK), Republic of Korea
  • Mahidol Oxford Tropical Medicine Research Unit (MORU), Thailand
  • Centre National de Recherche Scientifique (CNRS), France
  • University of Toulouse, France

Funding

  • Germany - Federal Ministry of Education and Research (BMBF) through KfW
​
  • Other private foundations and individuals
  • Wellcome
​

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