Evidence map›Paper›PMID 36233149›Full record

ArticleInternational journal of molecular sciences2022

Systematic Down-Selection of Repurposed Drug Candidates for COVID-19.

Christopher A MacRaild, Muzaffar-Ur-Rehman Mohammed, Faheem, Sankaranarayanan Murugesan, Ian K Styles, Amanda L Peterson, Carl M J Kirkpatrick, Matthew A Cooper, Enzo A Palombo, Moana M Simpson and 7 more

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
1.0field-weighted citation impact, top 23% 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

1 citing paper in PubMed, 11 citations in OpenAlex.

  1. Article
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

17 authors at 8 institutions in 4 countries.

Christopher A MacRaildDrug Delivery, Disposition and Dynamics, Monash Institute of Pharmaceutical Sciences, Monash University, Parkville, VIC 3800, Australia.ORCID 0000-0002-3694-3989
Muzaffar-Ur-Rehman MohammedDepartment of Pharmacy, Birla Institute of Technology and Science, Pilani Campus, Pilani 333031, Rajasthan, India.ORCID 0000-0002-5118-9005
FaheemDepartment of Pharmacy, Birla Institute of Technology and Science, Pilani Campus, Pilani 333031, Rajasthan, India.ORCID 0000-0002-2306-3050
Sankaranarayanan MurugesanDepartment of Pharmacy, Birla Institute of Technology and Science, Pilani Campus, Pilani 333031, Rajasthan, India.ORCID 0000-0002-3680-1577
Ian K StylesDrug Delivery, Disposition and Dynamics, Monash Institute of Pharmaceutical Sciences, Monash University, Parkville, VIC 3800, Australia.
Amanda L PetersonDrug Delivery, Disposition and Dynamics, Monash Institute of Pharmaceutical Sciences, Monash University, Parkville, VIC 3800, Australia.
Carl M J KirkpatrickCentre for Medicine Use and Safety, Monash Institute of Pharmaceutical Sciences, Monash University, Parkville, VIC 3800, Australia.
Matthew A CooperInstitute for Molecular Bioscience, The University of Queensland, Brisbane, QLD 4072, Australia.
Enzo A PalomboDepartment of Chemistry and Biotechnology, Swinburne University of Technology, Hawthorn, VIC 3122, Australia.ORCID 0000-0001-5889-1393
Moana M SimpsonGriffith Institute for Drug Discovery, Griffith University, Nathan, QLD 4111, Australia.
Hardik A JainDepartment of Electrical and Electronics Engineering, Birla Institute of Technology and Science, Pilani 333031, Rajasthan, India.ORCID 0000-0002-4129-3183
Vinti AgarwalDepartment of Computer Science and Information Systems, Birla Institute of Technology and Science, Pilani 333031, Rajasthan, India.
Alexander J McAuleyCommonwealth Scientific and Industrial Research Organisation, Australian Centre for Disease Preparedness, Portarlington Road, Geelong, VIC 3220, Australia.ORCID 0000-0002-7632-9633
Anupama KumarCommonwealth Scientific and Industrial Research Organisation, Land and Water, Waite Campus, SA 5064, Australia.
Darren J CreekDrug Delivery, Disposition and Dynamics, Monash Institute of Pharmaceutical Sciences, Monash University, Parkville, VIC 3800, Australia.ORCID 0000-0001-7497-7082
Natalie L TrevaskisDrug Delivery, Disposition and Dynamics, Monash Institute of Pharmaceutical Sciences, Monash University, Parkville, VIC 3800, Australia.ORCID 0000-0001-9538-549X
Seshadri S VasanCommonwealth Scientific and Industrial Research Organisation, Australian Centre for Disease Preparedness, Portarlington Road, Geelong, VIC 3220, Australia.ORCID 0000-0002-7326-3210
Monash University · AUBirla Institute of Technology and Science, Pilani · INCommonwealth Scientific and Industrial Research Organisation · AUGriffith University · AUSwinburne University of Technology · AUThe University of Melbourne · AUThe University of Queensland · AUUniversity of Utah · US

Funding

National Health and Medical Research Council MRF2009092United States Food and Drug Administration 75F40121C00144
6 · The paper itself

Abstract

SARS-CoV-2 is the cause of the COVID-19 pandemic which has claimed more than 6.5 million lives worldwide, devastating the economy and overwhelming healthcare systems globally. The development of new drug molecules and vaccines has played a critical role in managing the pandemic; however, new variants of concern still pose a significant threat as the current vaccines cannot prevent all infections. This situation calls for the collaboration of biomedical scientists and healthcare workers across the world. Repurposing approved drugs is an effective way of fast-tracking new treatments for recently emerged diseases. To this end, we have assembled and curated a database consisting of 7817 compounds from the Compounds Australia Open Drug collection. We developed a set of eight filters based on indicators of efficacy and safety that were applied sequentially to down-select drugs that showed promise for drug repurposing efforts against SARS-CoV-2. Considerable effort was made to evaluate approximately 14,000 assay data points for SARS-CoV-2 FDA/TGA-approved drugs and provide an average activity score for 3539 compounds. The filtering process identified 12 FDA-approved molecules with established safety profiles that have plausible mechanisms for treating COVID-19 disease. The methodology developed in our study provides a template for prioritising drug candidates that can be repurposed for the safe, efficacious, and cost-effective treatment of COVID-19, long COVID, or any other future disease. We present our database in an easy-to-use interactive interface (CoviRx that was also developed to enable the scientific community to access to the data of over 7000 potential drugs and to implement alternative prioritisation and down-selection strategies.

Indexed as

COVID-19COVID-19 Drug TreatmentAntiviral AgentsDrug RepositioningHumansPandemicsPost-Acute COVID-19 SyndromeSARS-CoV-2Antiviral AgentsCOVID-19CoviRx.orgdatabasedrugspandemicrepurposingSARS-CoV-2therapiestreatmentsVariants of Concern (VOC)

Identifiers

PMID36233149
PMCPMC9569752
OpenAlexW4303699317

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.