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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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Autor principal: Walker, Ulrich A
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2009
Materias:
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.
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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