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KAF156 is an antimalarial clinical candidate with potential for use in prophylaxis, treatment, and prevention of disease transmission.
Kuhen, Kelli L; Chatterjee, Arnab K; Rottmann, Matthias; Gagaring, Kerstin; Borboa, Rachel; Buenviaje, Jennifer; Chen, Zhong; Francek, Carolyn; Wu, Tao; Nagle, Advait; Barnes, S Whitney; Plouffe, David; Lee, Marcus C S; Fidock, David A; Graumans, Wouter; van de Vegte-Bolmer, Marga; van Gemert, Geert J; Wirjanata, Grennady; Sebayang, Boni; Marfurt, Jutta; Russell, Bruce; Suwanarusk, Rossarin; Price, Ric N; Nosten, Francois; Tungtaeng, Anchalee; Gettayacamin, Montip; Sattabongkot, Jetsumon; Taylor, Jennifer; Walker, John R; Tully, David; Patra, Kailash P; Flannery, Erika L; Vinetz, Joseph M; Renia, Laurent; Sauerwein, Robert W; Winzeler, Elizabeth A; Glynne, Richard J; Diagana, Thierry T.
Afiliação
  • Kuhen KL; Genomics Institute of the Novartis Research Foundation, San Diego, California, USA.
  • Chatterjee AK; Genomics Institute of the Novartis Research Foundation, San Diego, California, USA.
  • Rottmann M; Swiss Tropical and Public Health Institute, Parasite Chemotherapy, Basel, Switzerland University of Basel, Basel, Switzerland.
  • Gagaring K; Genomics Institute of the Novartis Research Foundation, San Diego, California, USA.
  • Borboa R; Genomics Institute of the Novartis Research Foundation, San Diego, California, USA.
  • Buenviaje J; Genomics Institute of the Novartis Research Foundation, San Diego, California, USA.
  • Chen Z; Genomics Institute of the Novartis Research Foundation, San Diego, California, USA.
  • Francek C; Genomics Institute of the Novartis Research Foundation, San Diego, California, USA.
  • Wu T; Genomics Institute of the Novartis Research Foundation, San Diego, California, USA.
  • Nagle A; Genomics Institute of the Novartis Research Foundation, San Diego, California, USA.
  • Barnes SW; Genomics Institute of the Novartis Research Foundation, San Diego, California, USA.
  • Plouffe D; Genomics Institute of the Novartis Research Foundation, San Diego, California, USA.
  • Lee MC; Department of Microbiology and Immunology, Columbia University College of Physicians and Surgeons, New York, New York, USA.
  • Fidock DA; Department of Microbiology and Immunology, Columbia University College of Physicians and Surgeons, New York, New York, USA Division of Infectious Diseases, Department of Medicine, Columbia University College of Physicians and Surgeons, New York, New York, USA.
  • Graumans W; Radboud University Nijmegen Medical Center, Medical Microbiology Department, Nijmegen, The Netherlands.
  • van de Vegte-Bolmer M; Radboud University Nijmegen Medical Center, Medical Microbiology Department, Nijmegen, The Netherlands.
  • van Gemert GJ; Radboud University Nijmegen Medical Center, Medical Microbiology Department, Nijmegen, The Netherlands.
  • Wirjanata G; Global Health Division, Menzies School of Health Research, Charles Darwin University, Darwin, Australia.
  • Sebayang B; Eijkman Institute for Molecular Biology, Jakarta, Indonesia.
  • Marfurt J; Global Health Division, Menzies School of Health Research, Charles Darwin University, Darwin, Australia.
  • Russell B; Laboratory of Malaria Immunobiology, Singapore Immunology Network, Agency for Science Technology and Research, Biopolis, Singapore.
  • Suwanarusk R; Laboratory of Malaria Immunobiology, Singapore Immunology Network, Agency for Science Technology and Research, Biopolis, Singapore.
  • Price RN; Global Health Division, Menzies School of Health Research, Charles Darwin University, Darwin, Australia Centre for Tropical Medicine, Nuffield Department of Clinical Medicine, University of Oxford, Oxford, United Kingdom.
  • Nosten F; Shoklo Malaria Research Unit, Mae Sot, Tak, Thailand Faculty of Tropical Medicine, Mahidol University, Bangkok, Thailand Centre for Tropical Medicine, Nuffield Department of Clinical Medicine, University of Oxford, Oxford, United Kingdom.
  • Tungtaeng A; Department of Veterinary Medicine, U.S. Army Medical Component, Armed Forces Research Institute of Medical Sciences, Bangkok, Thailand.
  • Gettayacamin M; Department of Veterinary Medicine, U.S. Army Medical Component, Armed Forces Research Institute of Medical Sciences, Bangkok, Thailand.
  • Sattabongkot J; Entomology Department, AFRIMS, Bangkok, Thailand Faculty of Tropical Medicine, Mahidol University, Bangkok, Thailand.
  • Taylor J; Genomics Institute of the Novartis Research Foundation, San Diego, California, USA.
  • Walker JR; Genomics Institute of the Novartis Research Foundation, San Diego, California, USA.
  • Tully D; Genomics Institute of the Novartis Research Foundation, San Diego, California, USA.
  • Patra KP; Division of Infectious Diseases, Department of Medicine, University of California, San Diego, La Jolla, California, USA.
  • Flannery EL; Division of Pharmacology and Drug Discovery, University of California, San Diego, School of Medicine, La Jolla, California, USA.
  • Vinetz JM; Division of Infectious Diseases, Department of Medicine, University of California, San Diego, La Jolla, California, USA.
  • Renia L; Laboratory of Malaria Immunobiology, Singapore Immunology Network, Agency for Science Technology and Research, Biopolis, Singapore.
  • Sauerwein RW; Radboud University Nijmegen Medical Center, Medical Microbiology Department, Nijmegen, The Netherlands.
  • Winzeler EA; Genomics Institute of the Novartis Research Foundation, San Diego, California, USA Division of Pharmacology and Drug Discovery, University of California, San Diego, School of Medicine, La Jolla, California, USA.
  • Glynne RJ; Genomics Institute of the Novartis Research Foundation, San Diego, California, USA.
  • Diagana TT; Novartis Institute for Tropical Diseases, Singapore thierry.diagana@novartis.com.
Antimicrob Agents Chemother ; 58(9): 5060-7, 2014 Sep.
Article em En | MEDLINE | ID: mdl-24913172
ABSTRACT
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.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Piperazinas / Malária Falciparum / Imidazóis / Antimaláricos Limite: Animals Idioma: En Ano de publicação: 2014 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Piperazinas / Malária Falciparum / Imidazóis / Antimaláricos Limite: Animals Idioma: En Ano de publicação: 2014 Tipo de documento: Article