Temsirolimus
| Clinical data | |
|---|---|
| Trade names | Torisel |
| Other names | CCI-779 |
| AHFS/Drugs.com | Monograph |
| MedlinePlus | a607071 |
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| Routes of administration | Intravenous |
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| Pharmacokinetic data | |
| Metabolism | Liver |
| Elimination half-life | 17.3 hours (temsirolimus); 54.6 hours (sirolimus)[2] |
| Excretion | Urine (4.6%), faeces (78%)[2] |
| Identifiers | |
IUPAC name
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| CompTox Dashboard (EPA) | |
| ECHA InfoCard | 100.211.882 |
| Chemical and physical data | |
| Formula | C56H87NO16 |
| Molar mass | 1030.303 g·mol−1 |
| (what is this?) (verify) | |
Temsirolimus, sold under the brand name Torisel, is an intravenous drug for the treatment of renal cell carcinoma (RCC), developed by Wyeth Pharmaceuticals and approved by the U.S. Food and Drug Administration (FDA) in May 2007,[3] and was also approved by the European Medicines Agency (EMA) in November 2007.[1] It is a derivative and prodrug of sirolimus.
- ^ a b "Torisel EPAR". European Medicines Agency. 17 September 2018. Retrieved 6 November 2020.
- ^ a b Temsirolimus Drug Monograph. Cancer Care Ontario. June 2014. p. 2.
- ^ "FDA Approves New Drug for Advanced Kidney Cancer" (Press release). U.S. Food and Drug Administration (FDA). May 30, 2007. Archived from the original on October 16, 2012. Retrieved October 15, 2013.