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itraconazole A synthetic triazole agent with antimycotic properties. Formulated for both topical and systemic use, itraconazole preferentially inhibits fugal cytochrome P450 enzymes, resulting in a decrease in fungal ergosterol synthesis. Because of its low toxicity profile, this agent can be used for long-term maintenance treatment of chronic fungal infections. Check for active clinical trials or closed clinical trials using this agent. (NCI Thesaurus)
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US brand name: | ![](https://webarchive.library.unt.edu/eot2008/20090115022603im_/http://www.cancer.gov/images/spacer.gif) | Sporanox | | ![](https://webarchive.library.unt.edu/eot2008/20090115022603im_/http://www.cancer.gov/images/spacer.gif) | Abbreviation: | ![](https://webarchive.library.unt.edu/eot2008/20090115022603im_/http://www.cancer.gov/images/spacer.gif) | ICZ | | ![](https://webarchive.library.unt.edu/eot2008/20090115022603im_/http://www.cancer.gov/images/spacer.gif) |
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