COVID-19 and a Tale of Three Drugs: To Repurpose, or Not to Repurpose-That Was the Question.

Publication date: Jun 23, 2025

On 11 March 2020, the World Health Organisation (WHO) declared a global pandemic caused by the SARS-CoV-2 coronavirus that earlier in February 2020 the WHO had named COVID-19 (coronavirus disease 2019). There were neither drugs nor vaccines that were known to be effective against the virus, stimulating an urgent worldwide search for treatments. An evaluation of existing drugs by ‘repurposing’ was initiated followed by a transition to de novo drug discovery. Repurposing of an already approved drug may accelerate the introduction of that drug into clinical use by circumventing early, including preclinical studies otherwise essential for a de novo drug and reducing development costs. Early in the pandemic three drugs were identified as repurposing candidates for the treatment of COVID-19: (i) hydroxychloroquine, an anti-malarial also used to treat rheumatoid arthritis and lupus; (ii) ivermectin, an antiparasitic approved for both human and veterinary use; (iii) remdesivir, an anti-viral originally developed to treat hepatitis C. The scientific evidence, both for and against the efficacy of these three drugs as treatments for COVID-19, vied with public demand and politicization as unqualified opinions clashed with evidence-based medicine. To quote Hippocrates, “There are in fact two things, science and opinion; the former begets knowledge, the latter ignorance”.

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Concepts Keywords
Arthritis Adenosine Monophosphate
Coronavirus Adenosine Monophosphate
February Alanine
Hydroxychloroquine Alanine
Antimalarials
Antimalarials
Antiviral Agents
Antiviral Agents
COVID-19
COVID-19
COVID-19 Drug Treatment
Drug Repositioning
Humans
Hydroxychloroquine
Hydroxychloroquine
hydroxychloroquine
Ivermectin
Ivermectin
ivermectin
remdesivir
remdesivir
repurposing
SARS-CoV-2

Semantics

Type Source Name
disease MESH COVID-19
drug DRUGBANK Hydroxychloroquine
disease MESH rheumatoid arthritis
pathway KEGG Rheumatoid arthritis
drug DRUGBANK Ivermectin
disease MESH hepatitis C
pathway KEGG Hepatitis C
disease MESH hepatitis
disease MESH panic
disease MESH Influenza
disease IDO entity
drug DRUGBANK Acetylsalicylic acid
drug DRUGBANK Thalidomide
disease MESH cancer
drug DRUGBANK Sildenafil
disease MESH erectile dysfunction
disease MESH pulmonary hypertension
disease MESH infection
disease IDO history
drug DRUGBANK Chloroquine
disease MESH malaria
pathway KEGG Malaria
drug DRUGBANK Metformin
pathway REACTOME Metabolism
disease IDO process
disease IDO parasite
drug DRUGBANK Azithromycin
disease MESH viral load
disease MESH cardiac arrhythmias
disease MESH emergency
disease MESH comorbidity
disease MESH systemic lupus erythematosus
pathway KEGG Systemic lupus erythematosus
disease MESH drug interactions
drug DRUGBANK Zinc
disease MESH death
drug DRUGBANK Dexamethasone
disease MESH parasitic infections
disease MESH river blindness
disease MESH onchocerciasis
disease MESH scabies
disease IDO replication
disease MESH dengue
disease IDO immunodeficiency
disease MESH viral disease
disease IDO blood
disease MESH Allergy
disease MESH Infectious Diseases
disease IDO intervention
disease MESH seizures
drug DRUGBANK Adenosine
drug DRUGBANK L-Alanine
disease IDO cell
drug DRUGBANK Lopinavir
drug DRUGBANK Ritonavir
drug DRUGBANK Interferon beta-1a
drug DRUGBANK Ranitidine
drug DRUGBANK Oxygen
disease MESH uncertainty
disease IDO site
disease MESH social vulnerability
disease MESH measles
pathway KEGG Measles
disease MESH vaccine preventable diseases
drug DRUGBANK Nonoxynol-9
pathway KEGG Coronavirus disease
disease MESH causes
drug DRUGBANK Guanosine
drug DRUGBANK Coenzyme M
drug DRUGBANK Efavirenz
disease MESH sudden cardiac death
disease MESH rheumatic diseases
drug DRUGBANK Ademetionine
disease MESH Arthritis
disease MESH anxiety
drug DRUGBANK Colchicine
drug DRUGBANK Sodium hydroxide
disease MESH Acute Kidney Injury
pathway REACTOME Release
drug DRUGBANK Adenosine phosphate

Original Article

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