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Revision as of 02:06, 1 September 2011 by BogBot (talk | contribs) (populated new fields in {{drugbox}} and reordered per bot approval. Report errors and suggestions to User_talk:BogBot)(diff) ← Previous revision | Latest revision (diff) | Newer revision → (diff) Pharmaceutical compoundClinical data | |
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AHFS/Drugs.com | Monograph |
MedlinePlus | a610013 |
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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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Chemical and physical data | |
Formula | C21H23N7O2S |
Molar mass | 437.517 g/mol g·mol |
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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 by the U.S. Food and Drug Administration. Pazopanib may also be active in ovarian cancer and soft tissue sarcoma. Pazopanib also appears effective in the treatment of non-small cell lung carcinoma.
References
- "FDA Approves GlaxoSmithKline's Votrient(TM) For Advanced Renal Cell Cancer". Medical News Today. 20 October 2009. Retrieved 8 June 2010.
- ^ "Pazopanib shows encouraging activity in several tumour types, including soft tissue sarcoma and ovarian cancer". FierceBiotech. 2008-09-15. Retrieved 2010-08-10.
- Attention: This template ({{cite doi}}) is deprecated. To cite the publication identified by doi:10.1200/JCO.2008.21.3223, please use {{cite journal}} (if it was published in a bona fide academic journal, otherwise {{cite report}} with
|doi=10.1200/JCO.2008.21.3223
instead.
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