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The global pipeline of new medicines for the control and elimination of malaria

Over the past decade, there has been a transformation in the portfolio of medicines to combat malaria. New fixed-dose artemisinin combination therapy is available, with four different types having received approval from Stringent Regulatory Authorities or the World Health Organization (WHO). However...

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Autores principales: Anthony, Melinda P, Burrows, Jeremy N, Duparc, Stephan, JMoehrle, Joerg, Wells, Timothy NC
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3472257/
https://www.ncbi.nlm.nih.gov/pubmed/22958514
http://dx.doi.org/10.1186/1475-2875-11-316
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author Anthony, Melinda P
Burrows, Jeremy N
Duparc, Stephan
JMoehrle, Joerg
Wells, Timothy NC
author_facet Anthony, Melinda P
Burrows, Jeremy N
Duparc, Stephan
JMoehrle, Joerg
Wells, Timothy NC
author_sort Anthony, Melinda P
collection PubMed
description Over the past decade, there has been a transformation in the portfolio of medicines to combat malaria. New fixed-dose artemisinin combination therapy is available, with four different types having received approval from Stringent Regulatory Authorities or the World Health Organization (WHO). However, there is still scope for improvement. The Malaria Eradication Research agenda identified several gaps in the current portfolio. Simpler regimens, such as a single-dose cure are needed, compared with the current three-day treatment. In addition, new medicines that prevent transmission and also relapse are needed, but with better safety profiles than current medicines. There is also a big opportunity for new medicines to prevent reinfection and to provide chemoprotection. This study reviews the global portfolio of new medicines in development against malaria, as of the summer of 2012. Cell-based phenotypic screening, and ‘fast followers’ of clinically validated classes, mean that there are now many new classes of molecules starting in clinical development, especially for the blood stages of malaria. There remain significant gaps for medicines blocking transmission, preventing relapse, and long-duration molecules for chemoprotection. The nascent pipeline of new medicines is significantly stronger than five years ago. However, there are still risks ahead in clinical development and sustainable funding of clinical studies is vital if this early promise is going to be delivered.
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spelling pubmed-34722572012-10-17 The global pipeline of new medicines for the control and elimination of malaria Anthony, Melinda P Burrows, Jeremy N Duparc, Stephan JMoehrle, Joerg Wells, Timothy NC Malar J Review Over the past decade, there has been a transformation in the portfolio of medicines to combat malaria. New fixed-dose artemisinin combination therapy is available, with four different types having received approval from Stringent Regulatory Authorities or the World Health Organization (WHO). However, there is still scope for improvement. The Malaria Eradication Research agenda identified several gaps in the current portfolio. Simpler regimens, such as a single-dose cure are needed, compared with the current three-day treatment. In addition, new medicines that prevent transmission and also relapse are needed, but with better safety profiles than current medicines. There is also a big opportunity for new medicines to prevent reinfection and to provide chemoprotection. This study reviews the global portfolio of new medicines in development against malaria, as of the summer of 2012. Cell-based phenotypic screening, and ‘fast followers’ of clinically validated classes, mean that there are now many new classes of molecules starting in clinical development, especially for the blood stages of malaria. There remain significant gaps for medicines blocking transmission, preventing relapse, and long-duration molecules for chemoprotection. The nascent pipeline of new medicines is significantly stronger than five years ago. However, there are still risks ahead in clinical development and sustainable funding of clinical studies is vital if this early promise is going to be delivered. BioMed Central 2012-09-07 /pmc/articles/PMC3472257/ /pubmed/22958514 http://dx.doi.org/10.1186/1475-2875-11-316 Text en Copyright ©2012 Anthony et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review
Anthony, Melinda P
Burrows, Jeremy N
Duparc, Stephan
JMoehrle, Joerg
Wells, Timothy NC
The global pipeline of new medicines for the control and elimination of malaria
title The global pipeline of new medicines for the control and elimination of malaria
title_full The global pipeline of new medicines for the control and elimination of malaria
title_fullStr The global pipeline of new medicines for the control and elimination of malaria
title_full_unstemmed The global pipeline of new medicines for the control and elimination of malaria
title_short The global pipeline of new medicines for the control and elimination of malaria
title_sort global pipeline of new medicines for the control and elimination of malaria
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3472257/
https://www.ncbi.nlm.nih.gov/pubmed/22958514
http://dx.doi.org/10.1186/1475-2875-11-316
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