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A dose-escalating phase II trial studied masitinib, an oral tyrosine kinase inhibitor, in 43 patients with rheumatoid arthritis. Masitinib induced American College of Rheumatology (ACR)20, ACR50 and ACR70 responses in 54%, 26% and 8% of patients, respectively. A placebo group was not included. Thirt...
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2009
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2745773/ https://www.ncbi.nlm.nih.gov/pubmed/19664170 http://dx.doi.org/10.1186/ar2734 |
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author | Walker, Ulrich A |
author_facet | Walker, Ulrich A |
author_sort | Walker, Ulrich A |
collection | PubMed |
description | A dose-escalating phase II trial studied masitinib, an oral tyrosine kinase inhibitor, in 43 patients with rheumatoid arthritis. Masitinib induced American College of Rheumatology (ACR)20, ACR50 and ACR70 responses in 54%, 26% and 8% of patients, respectively. A placebo group was not included. Thirty-seven per cent of the patients withdrew before the 12-week end-point was reached, primarily because of adverse events. These findings are the first on the efficacy of tyrosine kinase inhibition in a sizeable population. Future work should focus on delineating the tyrosine kinase that is most important in maintaining rheumatoid activity and address potential long-term toxicities such as gonadal insufficiency, teratogenicity and cardiotoxicity. |
format | Text |
id | pubmed-2745773 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-27457732009-09-18 More about masitinib Walker, Ulrich A Arthritis Res Ther Editorial A dose-escalating phase II trial studied masitinib, an oral tyrosine kinase inhibitor, in 43 patients with rheumatoid arthritis. Masitinib induced American College of Rheumatology (ACR)20, ACR50 and ACR70 responses in 54%, 26% and 8% of patients, respectively. A placebo group was not included. Thirty-seven per cent of the patients withdrew before the 12-week end-point was reached, primarily because of adverse events. These findings are the first on the efficacy of tyrosine kinase inhibition in a sizeable population. Future work should focus on delineating the tyrosine kinase that is most important in maintaining rheumatoid activity and address potential long-term toxicities such as gonadal insufficiency, teratogenicity and cardiotoxicity. BioMed Central 2009 2009-07-13 /pmc/articles/PMC2745773/ /pubmed/19664170 http://dx.doi.org/10.1186/ar2734 Text en Copyright © 2009 BioMed Central Ltd |
spellingShingle | Editorial Walker, Ulrich A More about masitinib |
title | More about masitinib |
title_full | More about masitinib |
title_fullStr | More about masitinib |
title_full_unstemmed | More about masitinib |
title_short | More about masitinib |
title_sort | more about masitinib |
topic | Editorial |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2745773/ https://www.ncbi.nlm.nih.gov/pubmed/19664170 http://dx.doi.org/10.1186/ar2734 |
work_keys_str_mv | AT walkerulricha moreaboutmasitinib |