Pazopanib hydrochloride
File:Pazopanib structure.svg | |
Clinical data | |
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Trade names | Votrient |
AHFS/Drugs.com | Monograph |
MedlinePlus | a610013 |
[[Regulation of therapeutic goods |Template:Engvar data]] | |
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Routes of administration | Oral |
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Pharmacokinetic data | |
Protein binding | >99% |
Metabolism | Hepatic (CYP3A4, 1A2 and 2C8-mediated) |
Elimination half-life | 31 hours (mean) |
Excretion | Mostly fecal |
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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 | C21H23N7O2S |
Molar mass | 437.517 g/mol |
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]
Overview
Pazopanib (trade name Votrient) is a potent and selective multi-targeted receptor tyrosine kinase inhibitor of VEGFR-1, VEGFR-2, VEGFR-3, PDGFR-a/β, and c-kit that blocks tumor growth and inhibits angiogenesis. It has been approved for renal cell carcinoma and soft tissue sarcoma by the U.S. Food and Drug Administration.[1][2][3] Pazopanib may also be active in ovarian cancer[4] Pazopanib also appears effective in the treatment of non-small cell lung carcinoma.[4]
References
- ↑ "FDA Approves GlaxoSmithKline's Votrient(TM) For Advanced Renal Cell Cancer". Medical News Today. 20 October 2009. Retrieved 8 June 2010.
- ↑ Template:Cite doi
- ↑ "FDA Approves Glaxo Cancer Drug Votrient". Reuters. 26 April 2012. Retrieved 27 April 2012.
- ↑ 4.0 4.1 "Pazopanib shows encouraging activity in several tumour types, including soft tissue sarcoma and ovarian cancer". FierceBiotech. 2008-09-15. Retrieved 2010-08-10.
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