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KAF156 is an antimalarial clinical candidate with potential for use in prophylaxis, treatment, and prevention of disease transmission

  • Kelli L. Kuhen
  • , Arnab K. Chatterjee
  • , Matthias Rottmann
  • , Kerstin Gagaring
  • , Rachel Borboa
  • , Jennifer Buenviaje
  • , Zhong Chen
  • , Carolyn Francek
  • , Tao Wu
  • , Advait Nagle
  • , S. Whitney Barnes
  • , David Plouffe
  • , Marcus C.S. Lee
  • , David A. Fidock
  • , Wouter Graumans
  • , Marga Van De Vegte-Bolmer
  • , Geert J. Van Gemert
  • , Grennady Wirjanata
  • , Boni Sebayang
  • , Jutta Marfurt
  • Bruce Russell, Rossarin Suwanarusk, Ric N. Price, Francois Nosten, Anchalee Tungtaeng, Montip Gettayacamin, Jetsumon Sattabongkot, Jennifer Taylor, John R. Walker, David Tully, Kailash P. Patra, Erika L. Flannery, Joseph M. Vinetz, Laurent Renia, Robert W. Sauerwein, Elizabeth A. Winzeler, Richard J. Glynne, Thierry T. Diagana
  • Genomics Institute of the Novartis Research Foundation
  • California Institute for Biomedical Research
  • Swiss Tropical and Public Health Institute Swiss TPH
  • University of Basel
  • Columbia University
  • Radboudumc
  • Menzies School of Health Research
  • Eijkman Institute for Molecular Biology
  • Agency for Science Technology and Research
  • University of Oxford
  • Shoklo Malaria Research Unit
  • Faculty of Tropical Medicine, Mahidol University
  • Armed Forces Research Institute of Medical Sciences (USAMC-AFRIMS)
  • Department of Medicine
  • University of California
  • Novartis Institute for Tropical Diseases Pte. Ltd.

Producción científica: Contribución a una revistaArtículorevisión exhaustiva

141 Citas (Scopus)

Resumen

Renewed global efforts toward malaria eradication have highlighted the need for novel antimalarial agents with activity against multiple stages of the parasite life cycle. We have previously reported the discovery of a novel class of antimalarial compounds in the imidazolopiperazine series that have activity in the prevention and treatment of blood stage infection in a mouse model of malaria. Consistent with the previously reported activity profile of this series, the clinical candidate KAF156 shows blood schizonticidal activity with 50% inhibitory concentrations of 6 to 17.4 nM against P. falciparum drug-sensitive and drug-resistant strains, as well as potent therapeutic activity in a mouse models of malaria with 50, 90, and 99% effective doses of 0.6, 0.9, and 1.4 mg/kg, respectively. When administered prophylactically in a sporozoite challenge mouse model, KAF156 is completely protective as a single oral dose of 10 mg/kg. Finally, KAF156 displays potent Plasmodium transmission blocking activities both in vitro and in vivo. Collectively, our data suggest that KAF156, currently under evaluation in clinical trials, has the potential to treat, prevent, and block the transmission of malaria.

Idioma originalInglés
Páginas (desde-hasta)5060-5067
Número de páginas8
PublicaciónAntimicrobial Agents and Chemotherapy
Volumen58
N.º9
DOI
EstadoPublicada - set. 2014
Publicado de forma externa

ODS de las Naciones Unidas

Este resultado contribuye a los siguientes Objetivos de Desarrollo Sostenible

  1. ODS 3: Salud y bienestar
    ODS 3: Salud y bienestar

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