Evidence map›Paper›PMID 37173515›Full record

ReviewNature reviews. Drug discovery2023

Accelerating antiviral drug discovery: lessons from COVID-19.

Annette von Delft, Matthew D Hall, Ann D Kwong, Lisa A Purcell, Kumar Singh Saikatendu, Uli Schmitz, John A Tallarico, Alpha A Lee

Open access · bronzeAbstract readReview
In one paragraph

Review in Nature reviews. Drug discovery, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 98 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
98citing papers in PubMed, 1 pooled it
33.8field-weighted citation impact, top 1% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

98 citing papers in PubMed, 1 synthesis or guideline pooled it, 174 citations in OpenAlex.

  1. Pooled it
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  15. Identification of Anti-Viral Compounds fromJournal of microbiology and biotechnology · 2026
    Article
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38 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors at 7 institutions in 3 countries.

Annette von Delft *Centre for Medicines Discovery, Nuffield Department of Medicine, University of Oxford, Oxford, UK. Annette.vondelft@cmd.ox.ac.uk.ORCID http://orcid.org/0000-0002-7699-8140
Matthew D HallNational Center for Advancing Translational Sciences, National Institutes of Health, Rockville, MD, USA.ORCID http://orcid.org/0000-0002-5073-442X
Ann D KwongPardes Biosciences, Carlsbad, CA, USA.
Lisa A PurcellVir Biotechnology, San Francisco, CA, USA.ORCID http://orcid.org/0000-0002-9565-2030
Kumar Singh SaikatenduDrug Discovery Sciences, Takeda California, Inc., San Diego, CA, USA.
Uli SchmitzGilead Sciences, Inc., Foster City, CA, USA.
John A TallaricoNovartis Institutes for Biomedical Research, Cambridge, MA, USA.
Alpha A Lee *PostEra, Inc., Cambridge, MA, USA. alpha.lee@postera.ai.
Bridge University · SSGilead Sciences (United States) · USNational Institute for Health Research · GBNational Institutes of Health · USNovartis (United States) · USTakeda (United States) · USVIR Biotechnology (United States) · US

Funding

Target enablementU19AI171399 · NIAID · SLOAN-KETTERING INST CAN RESEARCH · PI CHODERA, JOHN DAMON, LEE, ALPHA ALBERT · 2022 to 2025
$89.8M
COVID-19: Assay Development, HTS and Drug Repurposing to identify potential therapeutics against SARS-CoV-2ZIATR000457 · NCATS · NATIONAL CENTER FOR ADVANCING TRANSLATIONAL SCIENCES · PI HALL, MATTHEW · 2022 to 2023
$6.7M
NIAID NIH HHS U19 AI171399Wellcome Trust
6 · The paper itself

Abstract

During the coronavirus disease 2019 (COVID-19) pandemic, a wave of rapid and collaborative drug discovery efforts took place in academia and industry, culminating in several therapeutics being discovered, approved and deployed in a 2-year time frame. This article summarizes the collective experience of several pharmaceutical companies and academic collaborations that were active in severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) antiviral discovery. We outline our opinions and experiences on key stages in the small-molecule drug discovery process: target selection, medicinal chemistry, antiviral assays, animal efficacy and attempts to pre-empt resistance. We propose strategies that could accelerate future efforts and argue that a key bottleneck is the lack of quality chemical probes around understudied viral targets, which would serve as a starting point for drug discovery. Considering the small size of the viral proteome, comprehensively building an arsenal of probes for proteins in viruses of pandemic concern is a worthwhile and tractable challenge for the community.

Indexed as

COVID-19AnimalsAntiviral AgentsDrug DiscoveryPandemicsSARS-CoV-2Antiviral Agents

Identifiers

PMID37173515
PMCPMC10176316
OpenAlexW4376277283

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.