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Alemtuzumab
Alemtuzumab (Campath(®), MabCampath(®), Genzyme) is an IgG1k anti-CD52 humanized monoclonal antibody (mAb) that was first licensed in March 2001 by FDA. EMEA granted its approval in July 2001 and Health Canada in November 2005. The initial indication was limited to B-CLL previously treated and resis...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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2013
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7122495/ http://dx.doi.org/10.1007/978-88-470-5313-7_7 |
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author | Tridente, Giuseppe |
author_facet | Tridente, Giuseppe |
author_sort | Tridente, Giuseppe |
collection | PubMed |
description | Alemtuzumab (Campath(®), MabCampath(®), Genzyme) is an IgG1k anti-CD52 humanized monoclonal antibody (mAb) that was first licensed in March 2001 by FDA. EMEA granted its approval in July 2001 and Health Canada in November 2005. The initial indication was limited to B-CLL previously treated and resistant to alkylating agents. Starting from 2007, alemtuzumab was approved also as first-line therapy of B-CLL. So far, it has been experienced in over 60 countries. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/978-88-470-5313-7_7) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-7122495 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
record_format | MEDLINE/PubMed |
spelling | pubmed-71224952020-04-06 Alemtuzumab Tridente, Giuseppe Adverse Events with Biomedicines Article Alemtuzumab (Campath(®), MabCampath(®), Genzyme) is an IgG1k anti-CD52 humanized monoclonal antibody (mAb) that was first licensed in March 2001 by FDA. EMEA granted its approval in July 2001 and Health Canada in November 2005. The initial indication was limited to B-CLL previously treated and resistant to alkylating agents. Starting from 2007, alemtuzumab was approved also as first-line therapy of B-CLL. So far, it has been experienced in over 60 countries. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/978-88-470-5313-7_7) contains supplementary material, which is available to authorized users. 2013-07-12 /pmc/articles/PMC7122495/ http://dx.doi.org/10.1007/978-88-470-5313-7_7 Text en © Springer-Verlag Italia 2014 This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic. |
spellingShingle | Article Tridente, Giuseppe Alemtuzumab |
title | Alemtuzumab |
title_full | Alemtuzumab |
title_fullStr | Alemtuzumab |
title_full_unstemmed | Alemtuzumab |
title_short | Alemtuzumab |
title_sort | alemtuzumab |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7122495/ http://dx.doi.org/10.1007/978-88-470-5313-7_7 |
work_keys_str_mv | AT tridentegiuseppe alemtuzumab |