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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...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2012
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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. |
format | Online Article Text |
id | pubmed-3472257 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
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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