Difference between revisions of "Belinostat (Beleodaq)"

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(FDA approval)
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==History of changes in FDA indication==
 
==History of changes in FDA indication==
*7/3/2014: [http://www.fda.gov/newsevents/newsroom/pressannouncements/ucm403929.htm FDA accelerated approval] "for the treatment of patients with relapsed or refractory peripheral T-cell lymphoma (PTCL)."
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*7/3/2014: [http://www.fda.gov/newsevents/newsroom/pressannouncements/ucm403929.htm FDA accelerated approval] "for the treatment of patients with relapsed or refractory [[T-cell lymphoma | peripheral T-cell lymphoma (PTCL)]]."
  
 
==Also known as==
 
==Also known as==

Revision as of 03:31, 6 November 2014

General information

Class/mechanism: Histone deacetylase (HDAC) inhibitor. Belinostat causes cell cycle arrest and/or apoptosis of tumor cells by blocking HDAC, which results in accumulation of acetylated histones and other proteins.[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, 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

PXD101

References