Eltrombopag
| Clinical data | |
|---|---|
| Trade names | Promacta, Revolade, others | 
| Other names | SB-497115-GR | 
| AHFS/Drugs.com | Monograph | 
| MedlinePlus | a609011 | 
| License data | |
| Pregnancy category | 
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| Routes of administration | By mouth | 
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| Pharmacokinetic data | |
| Bioavailability | ~52% | 
| Protein binding | >99% | 
| Metabolism | extensive liver (through CYP1A2 and CYP2C8) | 
| Elimination half-life | 21–35 hours | 
| Excretion | feces (59%), urine (31%) | 
| Identifiers | |
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| CAS Number | 
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| DrugBank | 
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| ChemSpider | |
| UNII | 
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| ChEBI | |
| ChEMBL | 
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| CompTox Dashboard (EPA) | |
| ECHA InfoCard | 100.128.125 | 
| Chemical and physical data | |
| Formula | C25H22N4O4 | 
| Molar mass | 442.475 g·mol−1 | 
| 3D model (JSmol) | |
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| (what is this?) (verify) | |
Eltrombopag, sold under the brand name Promacta among others, is a medication used to treat thrombocytopenia (abnormally low platelet counts) and severe aplastic anemia. Eltrombopag is sold under the brand name Revolade outside the US and is marketed by Novartis. It is a thrombopoietin receptor agonist. It is taken by mouth.
Eltrombopag was discovered as a result of research collaboration between GlaxoSmithKline and Ligand Pharmaceuticals and is transferred to Novartis Pharmaceuticals.