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Need for a standardized translational drug development platform: lessons learned from the repurposing of drugs for COVID-19

Abstract:
In the absence of drugs to treat or prevent COVID-19, drug repurposing can be a valuable strategy. Despite a substantial number of clinical trials, drug repurposing did not deliver on its promise. While success was observed with some repurposed drugs (e.g., remdesivir, dexamethasone, tocilizumab, baricitinib), others failed to show clinical efficacy. One reason is the lack of clear translational processes based on adequate preclinical profiling before clinical evaluation. Combined with limitations of existing in vitro and in vivo models, there is a need for a systematic approach to urgent antiviral drug development in the context of a global pandemic. We implemented a methodology to test repurposed and experimental drugs to generate robust preclinical evidence for further clinical development. This translational drug development platform comprises in vitro, ex vivo, and in vivo models of SARS-CoV-2, along with pharmacokinetic modeling and simulation approaches to evaluate exposure levels in plasma and target organs. Here, we provide examples of identified repurposed antiviral drugs tested within our multidisciplinary collaboration to highlight lessons learned in urgent antiviral drug development during the COVID-19 pandemic. Our data confirm the importance of assessing in vitro and in vivo potency in multiple assays to boost the translatability of pre-clinical data. The value of pharmacokinetic modeling and simulations for compound prioritization is also discussed. We advocate the need for a standardized translational drug development platform for mild-to-moderate COVID-19 to generate preclinical evidence in support of clinical trials. We propose clear prerequisites for progression of drug candidates for repurposing into clinical trials. Further research is needed to gain a deeper understanding of the scope and limitations of the presented translational drug development platform.
Publication status:
Published
Peer review status:
Peer reviewed

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Publisher copy:
10.3390/microorganisms10081639

Authors

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Institution:
University of Oxford
Division:
MSD
Department:
NDM
Sub department:
Tropical Medicine
Role:
Author
ORCID:
0000-0002-1146-3452
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Role:
Author
ORCID:
0000-0003-2326-2938
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Role:
Author
ORCID:
0000-0001-9771-7312
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Role:
Author
ORCID:
0000-0001-8820-6617
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Role:
Author
ORCID:
0000-0002-4734-2249


Publisher:
MDPI
Journal:
Microorganisms More from this journal
Volume:
10
Issue:
8
Article number:
1639
Publication date:
2022-08-12
Acceptance date:
2022-08-04
DOI:
EISSN:
2076-2607
Pmid:
36014057


Language:
English
Keywords:
Pubs id:
1276433
Local pid:
pubs:1276433
Deposit date:
2023-01-09
ARK identifier:

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