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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 |
Appears in Collections: | Staff Publications Elements |
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