Vorinostat: Difference between revisions
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Revision as of 17:25, 20 August 2012
File:Vorinostat.svg | |
Clinical data | |
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[[Regulation of therapeutic goods |Template:Engvar data]] |
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Routes of administration | Oral |
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Pharmacokinetic data | |
Protein binding | 71% |
Metabolism | Hepatic glucuronidation and oxidation CYP system not involved |
Elimination half-life | 2 hours |
Excretion | Renal (negligible) |
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E number | {{#property:P628}} |
ECHA InfoCard | {{#property:P2566}}Lua error in Module:EditAtWikidata at line 36: attempt to index field 'wikibase' (a nil value). |
Chemical and physical data | |
Formula | C14H20N2O3 |
Molar mass | 264.32 g/mol |
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Clinical Trials |
Ongoing Trials on Vorinostat at Clinical Trials.gov Clinical Trials on Vorinostat at Google
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US National Guidelines Clearinghouse on Vorinostat
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Patient resources on Vorinostat Discussion groups on Vorinostat Patient Handouts on Vorinostat Directions to Hospitals Treating Vorinostat Risk calculators and risk factors for Vorinostat
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Overview
Vorinostat (rINN) or suberoylanilide hydroxamic acid (SAHA), brand name Zolinza®, is a drug currently under investigation for the treatment of cutaneous T cell lymphoma (CTCL), a type of skin cancer, to be used when the disease persists, gets worse, or comes back during or after treatment with other medicines. It is the first in a new class of agents known as histone deacetylase inhibitors.
A recent study suggested that vorinostat also possesses some activity against recurrent glioblastoma multiforme, resulting in a median overall survival of 5.7 months (compared to 4 - 4.4 months in earlier studies). Further brain tumor trials are planned in which vorinostat will be combined with other drugs.
Zolinza was approved by the U.S. Food and Drug Administration (FDA) for the treatment of CTCL on October 6, 2006, and it is manufactured by Pantheon, Inc., in Mississauga, Ontario, Canada, for Merck & Co., Inc., White House Station, New Jersey.
References
- "ZOLINZA™, Merck's Investigational Medicine for Advanced Cutaneous T-Cell Lymphoma (CTCL), To Receive Priority Review from U.S. Food and Drug Administration" (Press release). Merck & Co. June 7, 2006. Retrieved 2006-10-06.
- "FDA Approves New Drug for Skin Cancer, Zolinza" (Press release). Food and Drug Administration. October 6, 2006. Retrieved 2006-10-06.
- "Vorinostat shows anti-cancer activity in recurrent gliomas" (Press release). Mayo Clinic. June 3, 2007. Retrieved 2007-06-03.
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- Chemotherapeutic agents
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- Hydroxamic acids