Bexarotene
| Clinical data | |
|---|---|
| Trade names | Targretin | 
| AHFS/Drugs.com | Monograph | 
| MedlinePlus | a608006 | 
| License data | 
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| Routes of administration | By mouth, topical | 
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| Pharmacokinetic data | |
| Protein binding | >99% | 
| Metabolism | Hepatic (CYP3A4-mediated) | 
| Elimination half-life | 7 hours | 
| Excretion | Parent drug and metabolites are eliminated primarily through the hepatobiliary system. Less than 1% is excreted in the urine unchanged. | 
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| CompTox Dashboard (EPA) | |
| ECHA InfoCard | 100.206.790 | 
| Chemical and physical data | |
| Formula | C24H28O2 | 
| Molar mass | 348.486 g·mol−1 | 
| 3D model (JSmol) | |
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Bexarotene, sold under the brand Targretin, is an antineoplastic (anti-cancer) agent used for the treatment of cutaneous T cell lymphoma (CTCL). It is a third-generation retinoid.
It was approved by the U.S. Food and Drug Administration (FDA) in December 1999, and the European Medicines Agency (EMA) in March 2001. It is available as a generic medication.