Erik De Clercq

Dr. Erik De Clercq

Rega Institute for Medical Research, Katholieke Universiteit Leuven, Herestraat 49 box 1030, B-3000 Leuven, Belgium
orcid

Research Focus & Metrics

Academic Career Length

60Years (1967-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 August 1988 in Journal of Virological Methods
Verified
Journal Article
Closed access
RPRudi Pauwels
Rudi Pauwels
JBJan Balzarini
Jan Balzarini
MBMasanori Baba
Masanori Baba
RSRobert Snoeck
Robert Snoeck
DSDomique Schols
Domique Schols
Erik De ClercqErik De Clercq
Erik De Clercq

10 February 2020 in Nature Reviews Drug Discovery
Verified
Journal Article
Closed access
GLGuangdi Li
Guangdi Li
Erik De ClercqErik De Clercq
Erik De Clercq

1 July 2016 in Clinical Microbiology Reviews
Verified
Journal Article
Closed access
PDF file
Erik De ClercqErik De Clercq
Erik De Clercq
GLGuangdi Li
Guangdi Li
SUMMARY Since the first antiviral drug, idoxuridine, was approved in 1963, 90 antiviral drugs categorized into 13 functional groups have been formally approved for the treatment of the following 9 human infectious diseases: (i) HIV infections (protease inhibitors, integrase inhibitors, entry inhibitors, nucleoside reverse transcriptase inhibitors, nonnucleoside reverse transcriptase inhibitors, and acyclic nucleoside phosphonate analogues), (ii) hepatitis B virus (HBV) infections (lamivudine, interferons, nucleoside analogues, and acyclic nucleoside phosphonate analogues), (iii) hepatitis C virus (HCV) infections (ribavirin, interferons, NS3/4A protease inhibitors, NS5A inhibitors, and NS5B polymerase inhibitors), (iv) herpesvirus infections (5-substituted 2′-deoxyuridine analogues, entry inhibitors, nucleoside analogues, pyrophosphate analogues, and acyclic guanosine analogues), (v) influenza virus infections (ribavirin, matrix 2 protein inhibitors, RNA polymerase inhibitors, and neuraminidase inhibitors), (vi) human cytomegalovirus infections (acyclic guanosine analogues, acyclic nucleoside phosphonate analogues, pyrophosphate analogues, and oligonucleotides), (vii) varicella-zoster virus infections (acyclic guanosine analogues, nucleoside analogues, 5-substituted 2′-deoxyuridine analogues, and antibodies), (viii) respiratory syncytial virus infections (ribavirin and antibodies), and (ix) external anogenital warts caused by human papillomavirus infections (imiquimod, sinecatechins, and podofilox). Here, we present for the first time a comprehensive overview of antiviral drugs approved over the past 50 years, shedding light on the development of effective antiviral treatments against current and emerging infectious diseases worldwide.

1 July 2001 in Nature Neuroscience
Verified
Journal Article
Closed access
PDF file
PBPaola Bezzi
Paola Bezzi
MDMaria Domercq
Maria Domercq
LBLiliana Brambilla
Liliana Brambilla
RGRossella Galli
Rossella Galli
DSDomique Schols
Domique Schols
AVAndrea Volterra
Andrea Volterra

1 June 2004 in Journal of Clinical Virology
Verified
Journal Article
Closed access
Erik De ClercqErik De Clercq
Erik De Clercq

19 April 2023 in Nature Reviews Drug Discovery
Verified
Journal Article
Open access
PDF file
GLGuangdi Li
Guangdi Li
RHRolf Hilgenfeld
Rolf Hilgenfeld
RWRichard Whitley
Richard Whitley
Erik De ClercqErik De Clercq
Erik De Clercq
The coronavirus disease 2019 (COVID-19) pandemic has stimulated tremendous efforts to develop therapeutic strategies that target severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) and/or human proteins to control viral infection, encompassing hundreds of potential drugs and thousands of patients in clinical trials. So far, a few small-molecule antiviral drugs (nirmatrelvir–ritonavir, remdesivir and molnupiravir) and 11 monoclonal antibodies have been marketed for the treatment of COVID-19, mostly requiring administration within 10 days of symptom onset. In addition, hospitalized patients with severe or critical COVID-19 may benefit from treatment with previously approved immunomodulatory drugs, including glucocorticoids such as dexamethasone, cytokine antagonists such as tocilizumab and Janus kinase inhibitors such as baricitinib. Here, we summarize progress with COVID-19 drug discovery, based on accumulated findings since the pandemic began and a comprehensive list of clinical and preclinical inhibitors with anti-coronavirus activities. We also discuss the lessons learned from COVID-19 and other infectious diseases with regard to drug repurposing strategies, pan-coronavirus drug targets, in vitro assays and animal models, and platform trial design for the development of therapeutics to tackle COVID-19, long COVID and pathogenic coronaviruses in future outbreaks.