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Identification of targets and new developments in the treatment of multiple sclerosis – focus on cladribine
Orally available disease-modifying drugs for relapsing-remitting multiple sclerosis (MS) represent an unmet need for this chronic and debilitating disease. Among 5 currently investigated drugs at phase 3 clinical stage, promising efficacy data for fingolimod and oral cladribine have recently been pu...
Autores principales: | , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2010
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2915536/ https://www.ncbi.nlm.nih.gov/pubmed/20689698 |
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author | Warnke, Clemens Wiendl, Heinz Hartung, Hans-Peter Stüve, Olaf Kieseier, Bernd C |
author_facet | Warnke, Clemens Wiendl, Heinz Hartung, Hans-Peter Stüve, Olaf Kieseier, Bernd C |
author_sort | Warnke, Clemens |
collection | PubMed |
description | Orally available disease-modifying drugs for relapsing-remitting multiple sclerosis (MS) represent an unmet need for this chronic and debilitating disease. Among 5 currently investigated drugs at phase 3 clinical stage, promising efficacy data for fingolimod and oral cladribine have recently been published. However, benefits need to be weighed against the risks to define the role of these compounds within current treatment regimens. In this review, data on the efficacy of a promising compound, oral cladribine, are discussed and balanced with known and anticipated risks in a postmarketing era, and finally gives an outlook on the potential place of this drug in treatment algorithms for MS in the future. |
format | Text |
id | pubmed-2915536 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-29155362010-08-05 Identification of targets and new developments in the treatment of multiple sclerosis – focus on cladribine Warnke, Clemens Wiendl, Heinz Hartung, Hans-Peter Stüve, Olaf Kieseier, Bernd C Drug Des Devel Ther Review Orally available disease-modifying drugs for relapsing-remitting multiple sclerosis (MS) represent an unmet need for this chronic and debilitating disease. Among 5 currently investigated drugs at phase 3 clinical stage, promising efficacy data for fingolimod and oral cladribine have recently been published. However, benefits need to be weighed against the risks to define the role of these compounds within current treatment regimens. In this review, data on the efficacy of a promising compound, oral cladribine, are discussed and balanced with known and anticipated risks in a postmarketing era, and finally gives an outlook on the potential place of this drug in treatment algorithms for MS in the future. Dove Medical Press 2010-07-21 /pmc/articles/PMC2915536/ /pubmed/20689698 Text en © 2010 Warnke et al, publisher and licensee Dove Medical Press Ltd. This is an Open Access article which permits unrestricted noncommercial use, provided the original work is properly cited. |
spellingShingle | Review Warnke, Clemens Wiendl, Heinz Hartung, Hans-Peter Stüve, Olaf Kieseier, Bernd C Identification of targets and new developments in the treatment of multiple sclerosis – focus on cladribine |
title | Identification of targets and new developments in the treatment of multiple sclerosis – focus on cladribine |
title_full | Identification of targets and new developments in the treatment of multiple sclerosis – focus on cladribine |
title_fullStr | Identification of targets and new developments in the treatment of multiple sclerosis – focus on cladribine |
title_full_unstemmed | Identification of targets and new developments in the treatment of multiple sclerosis – focus on cladribine |
title_short | Identification of targets and new developments in the treatment of multiple sclerosis – focus on cladribine |
title_sort | identification of targets and new developments in the treatment of multiple sclerosis – focus on cladribine |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2915536/ https://www.ncbi.nlm.nih.gov/pubmed/20689698 |
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