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AWZ1066S, a highly specific anti-Wolbachia drug candidate for a short-course treatment of filariasis

  • W. David Hong
  • , Farid Benayoud
  • , Gemma L. Nixon
  • , Louise Ford
  • , Kelly L. Johnston
  • , Rachel H. Clare
  • , Andrew Cassidy
  • , Darren A.N. Cook
  • , Amy Siu
  • , Motohiro Shiotani
  • , Peter J.H. Webborn
  • , Stefan Kavanagh
  • , Ghaith Aljayyoussi
  • , Emma Murphy
  • , Andrew Steven
  • , John Archer
  • , Dominique Struever
  • , Stefan J. Frohberger
  • , Alexandra Ehrens
  • , Marc P. Hübner
  • Achim Hoerauf, Adam P. Roberts, Alasdair T.M. Hubbard, Edward W. Tate, Remigiusz A. Serwa, Suet C. Leung, Li Qie, Neil G. Berry, Fabian Gusovsky, Janet Hemingway*, Joseph D. Turner, Mark J. Taylor, Stephen A. Ward, Paul M. O’Neill
*Corresponding author for this work
  • University of Liverpool
  • Liverpool School of Tropical Medicine
  • Eisai Inc.
  • Department of Parasitology
  • Eisai Co. Ltd.
  • AstraZeneca
  • PJHW Consultancy Ltd.
  • University of Bonn
  • Imperial College London

Research output: Contribution to journalArticle (journal)peer-review

Abstract

Onchocerciasis and lymphatic filariasis are two neglected tropical diseases that together affect ∼157 million people and inflict severe disability. Both diseases are caused by parasitic filarial nematodes with elimination efforts constrained by the lack of a safe drug that can kill the adult filaria (macrofilaricide). Previous proof-of-concept human trials have demonstrated that depleting >90% of the essential nematode endosymbiont bacterium, Wolbachia, using antibiotics, can lead to permanent sterilization of adult female parasites and a safe macrofilaricidal outcome. AWZ1066S is a highly specific anti-Wolbachia candidate selected through a lead optimization program focused on balancing efficacy, safety and drug metabolism/pharmacokinetic (DMPK) features of a thienopyrimidine/quinazoline scaffold derived from phenotypic screening. AWZ1066S shows superior efficacy to existing anti-Wolbachia therapies in validated preclinical models of infection and has DMPK characteristics that are compatible with a short therapeutic regimen of 7 days or less. This candidate molecule is well-positioned for onward development and has the potential to make a significant impact on communities affected by filariasis.

Original languageEnglish
Pages (from-to)1414-1419
Number of pages6
JournalProceedings of the National Academy of Sciences of the United States of America
Volume116
Issue number4
DOIs
Publication statusPublished - 22 Jan 2019

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • Anti-Wolbachia
  • Drug discovery
  • Lymphatic filariasis
  • Macrofilaricide
  • Onchocerciasis

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