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Discovery of JNJ-1802, a First-in-Class Pan-Serotype Dengue Virus NS4B Inhibitor

Authors
  • Kesteleyn, Bart;
  • Bonfanti, Jean-Francois;
  • Bardiot, Dorothee;
  • De Boeck, Benoit;
  • Goethals, Olivia;
  • Kaptein, Suzanne J.F.; 51996;
  • Stoops, Bart;
  • Coesemans, Erwin;
  • Fortin, Jerome;
  • Muller, Philippe;
  • Doublet, Frederic;
  • Carlens, Gunter;
  • Koukni, Mohamed;
  • Smets, Wim;
  • Raboisson, Pierre;
  • Chaltin, Patrick;
  • Simmen, Kenny;
  • Van Loock, Marnix;
  • Neyts, Johan; 14425;
  • Marchand, Arnaud;
  • And 1 more
Publication Date
Feb 28, 2024
Source
Lirias
Keywords
Language
English
License
Unknown
External links

Abstract

Dengue is a global public health threat, with about half of the world's population at risk of contracting this mosquito-borne viral disease. Climate change, urbanization, and global travel accelerate the spread of dengue virus (DENV) to new areas, including southern parts of Europe and the US. Currently, no dengue-specific small-molecule antiviral for prophylaxis or treatment is available. Here, we report the discovery of JNJ-1802 as a potent, pan-serotype DENV inhibitor (EC50's ranging from 0.057 to 11 nM against the four DENV serotypes). The observed oral bioavailability of JNJ-1802 across preclinical species, its low clearance in human hepatocytes, the absence of major in vitro pharmacology safety alerts, and a dose-proportional increase in efficacy against DENV-2 infection in mice were all supportive of its selection as a development candidate against dengue. JNJ-1802 is being progressed in clinical studies for the prevention or treatment of dengue. / status: published

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