Regorafenib
| Clinical data | |
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| Trade names | Stivarga, Regonix |
| Other names | BAY 73-4506 |
| AHFS/Drugs.com | Monograph |
| MedlinePlus | a613004 |
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| Routes of administration | By mouth |
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| Pharmacokinetic data | |
| Bioavailability | 69-83% |
| Protein binding | 99.5% |
| Metabolism | Liver (UGT1A9-mediated) |
| Elimination half-life | 20-30 hours |
| Excretion | Feces (71%), urine (19%) |
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| CompTox Dashboard (EPA) | |
| ECHA InfoCard | 100.248.939 |
| Chemical and physical data | |
| Formula | C21H15ClF4N4O3 |
| Molar mass | 482.82 g·mol−1 |
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Regorafenib, sold under the brand name Stivarga among others, is an oral multi-kinase inhibitor developed by Bayer which targets angiogenic, stromal and oncogenic receptor tyrosine kinase (RTK). Regorafenib shows anti-angiogenic activity due to its dual targeted VEGFR2-TIE2 tyrosine kinase inhibition. Since 2009 it was studied as a potential treatment option in multiple tumor types. By 2015 it had two US approvals for advanced cancers.