Difference between revisions of "Alemtuzumab (Campath)"

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==History of changes in FDA indication==
 
==History of changes in FDA indication==
*5/7/2001: Initial approval "for the treatment of patients with B-cell chronic lymphocytic leukemia who have been treated with alkylating agents and who have failed fludarabine therapy."<ref>[http://www.accessdata.fda.gov/drugsatfda_docs/appletter/2001/alemmil050701L.htm FDA approval letter dated May 7th, 2001]</ref>
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*5/7/2001: Initial approval "for the treatment of patients with [[Chronic lymphocytic leukemia (CLL) and Small lymphocytic lymphoma (SLL) | B-cell chronic lymphocytic leukemia]] who have been treated with [http://hemonc.org/wiki/Category:Alkylating_agents alkylating agents] and who have failed [[Fludarabine (Fludara) | fludarabine]] therapy."<ref>[http://www.accessdata.fda.gov/drugsatfda_docs/appletter/2001/alemmil050701L.htm FDA approval letter dated May 7th, 2001]</ref>
*9/19/2007: Indication expanded "to include use as a single agent for treatment of B-cell chronic lymphocytic leukemia (B-CLL)"
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*9/19/2007: Indication expanded "to include use as a single agent for treatment of [[Chronic lymphocytic leukemia (CLL) and Small lymphocytic lymphoma (SLL) | B-cell chronic lymphocytic leukemia (B-CLL)]]"
 
*October 2012: Genzyme withdraws drug from USA and EU (still available for B-CLL patients, however).  See Lancet editorial.<ref>[http://www.thelancet.com/journals/lancet/article/PIIS0140-6736(12)61776-0/fulltext Alemtuzumab for multiple sclerosis]</ref>
 
*October 2012: Genzyme withdraws drug from USA and EU (still available for B-CLL patients, however).  See Lancet editorial.<ref>[http://www.thelancet.com/journals/lancet/article/PIIS0140-6736(12)61776-0/fulltext Alemtuzumab for multiple sclerosis]</ref>
  
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[[Category:Antibody medications]]
 
[[Category:Antibody medications]]
 
[[Category:Chronic lymphocytic leukemia (CLL) and Small lymphocytic lymphoma (SLL) medications]]
 
[[Category:Chronic lymphocytic leukemia (CLL) and Small lymphocytic lymphoma (SLL) medications]]
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[[Category:Myelodysplastic syndrome medications]]
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[[Category:Drugs FDA approved in 2001]]

Revision as of 21:09, 5 November 2014

General information

Class/mechanism: Anti-CD52 antibody that is believed to cause antibody-dependent cell-mediated cytotoxicity of cells that express the CD52 antigen on their surface: B and T lymphocytes, most monocytes, macrophages, natural killer (NK) cells, and a subpopulation of granulocytes.[1][2][3]
Route: IV
Extravasation: no information

For conciseness and simplicity, HemOnc.org currently will focus on treatment regimens and not list information such as: renal/hepatic dose adjustments, metabolism (including CYP450), excretion, monitoring parameters (although this will be considered for checklists), or manufacturer. Instead, for the most current information, please refer to your preferred pharmacopeias such as Micromedex, Lexicomp, Medscape, UpToDate (courtesy of Lexicomp), or the prescribing information.[1]

Diseases for which it is used

Patient drug information

History of changes in FDA indication

Also known as

Precise Name: alemtuzumab (RXCUI 117055)

Campath, Campath-1H, Lemtrada, Mabcampath

References