Use of quantitative pharmacology tools to improve malaria treatments

The use of pharmacokinetic (PK) and pharmacodynamic (PD) data to inform antimalarial treatment regimens has accelerated in the past few decades, due in no small part to the stimulus provided by progressive development of parasite resistance to most of the currently available drugs. An understanding...

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Main Authors: Davis, T., Moore, B., Salman, S., Page-Sharp, Madhu, Batty, Kevin, Manning, L.
Format: Journal Article
Published: 2015
Online Access:http://hdl.handle.net/20.500.11937/16310
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author Davis, T.
Moore, B.
Salman, S.
Page-Sharp, Madhu
Batty, Kevin
Manning, L.
author_facet Davis, T.
Moore, B.
Salman, S.
Page-Sharp, Madhu
Batty, Kevin
Manning, L.
author_sort Davis, T.
building Curtin Institutional Repository
collection Online Access
description The use of pharmacokinetic (PK) and pharmacodynamic (PD) data to inform antimalarial treatment regimens has accelerated in the past few decades, due in no small part to the stimulus provided by progressive development of parasite resistance to most of the currently available drugs. An understanding of the disposition, interactions, efficacy and toxicity of the mainstay of contemporary antimalarial treatment, artemisinin combination therapy (ACT), has been facilitated by PK/PD studies which have been used to refine treatment regimens across the spectrum of disease, especially in special groups including young children and pregnant women. The present review highlights recent clinically-important examples of the ways in which these quantitative pharmacology tools have been applied to improve ACT, as well as 8-aminoquinoline use and the characterisation of novel antimalarial therapies such as the spiroindolones.
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spelling curtin-20.500.11937-163102017-09-13T15:04:07Z Use of quantitative pharmacology tools to improve malaria treatments Davis, T. Moore, B. Salman, S. Page-Sharp, Madhu Batty, Kevin Manning, L. The use of pharmacokinetic (PK) and pharmacodynamic (PD) data to inform antimalarial treatment regimens has accelerated in the past few decades, due in no small part to the stimulus provided by progressive development of parasite resistance to most of the currently available drugs. An understanding of the disposition, interactions, efficacy and toxicity of the mainstay of contemporary antimalarial treatment, artemisinin combination therapy (ACT), has been facilitated by PK/PD studies which have been used to refine treatment regimens across the spectrum of disease, especially in special groups including young children and pregnant women. The present review highlights recent clinically-important examples of the ways in which these quantitative pharmacology tools have been applied to improve ACT, as well as 8-aminoquinoline use and the characterisation of novel antimalarial therapies such as the spiroindolones. 2015 Journal Article http://hdl.handle.net/20.500.11937/16310 10.1586/17512433.2016.1129273 restricted
spellingShingle Davis, T.
Moore, B.
Salman, S.
Page-Sharp, Madhu
Batty, Kevin
Manning, L.
Use of quantitative pharmacology tools to improve malaria treatments
title Use of quantitative pharmacology tools to improve malaria treatments
title_full Use of quantitative pharmacology tools to improve malaria treatments
title_fullStr Use of quantitative pharmacology tools to improve malaria treatments
title_full_unstemmed Use of quantitative pharmacology tools to improve malaria treatments
title_short Use of quantitative pharmacology tools to improve malaria treatments
title_sort use of quantitative pharmacology tools to improve malaria treatments
url http://hdl.handle.net/20.500.11937/16310