Please use this identifier to cite or link to this item: https://doi.org/10.1128/AAC.02727-13
Title: KAF156 is an antimalarial clinical candidate with potential for use in prophylaxis, treatment, and prevention of disease transmission
Authors: Kuhen, K.L
Chatterjee, A.K
Rottmann, M
Keywords: antimalarial agent
artesunate
chloroquine
imidazole derivative
kaf 156
kaf156
mefloquine
piperazine derivative
unclassified drug
antimalarial agent
imidazole derivative
KAF156
piperazine derivative
animal experiment
animal model
Anopheles
antimalarial activity
antimalarial drug susceptibility
article
controlled study
disease elimination
dose time effect relation
drug dose comparison
drug efficacy
drug safety
female
genetic strain
human
human cell
IC 50
in vitro study
in vivo study
malaria control
malaria falciparum
mouse
multiple drug dose
nonhuman
parasite clearance
parasite transmission
Plasmodium falciparum
Plasmodium vivax malaria
priority journal
rodent malaria
schizont
single drug dose
sporozoite
treatment response
animal
drug effects
IC50
Institute for Cancer Research mouse
Malaria, Falciparum
transmission
Animals
Antimalarials
Imidazoles
Inhibitory Concentration 50
Malaria, Falciparum
Mice
Mice, Inbred ICR
Piperazines
Plasmodium falciparum
Sporozoites
Issue Date: 2014
Publisher: American Society for Microbiology
Citation: Kuhen, K.L, Chatterjee, A.K, Rottmann, M (2014). KAF156 is an antimalarial clinical candidate with potential for use in prophylaxis, treatment, and prevention of disease transmission. Antimicrobial Agents and Chemotherapy 58 (9) : 5060-5067. ScholarBank@NUS Repository. https://doi.org/10.1128/AAC.02727-13
Rights: Attribution 4.0 International
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. Copyright © 2014 Kuhen et al.
Source Title: Antimicrobial Agents and Chemotherapy
URI: https://scholarbank.nus.edu.sg/handle/10635/180171
ISSN: 0066-4804
DOI: 10.1128/AAC.02727-13
Rights: Attribution 4.0 International
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