Baricitinib
| Clinical data | |||
|---|---|---|---|
| Trade names | Olumiant, others | ||
| Other names | INCB28050, LY3009104 | ||
| AHFS/Drugs.com | Monograph | ||
| MedlinePlus | a618033 | ||
| License data | 
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| Pregnancy category | 
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| Routes of administration | By mouth | ||
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| Pharmacokinetic data | |||
| Bioavailability | 79% | ||
| Protein binding | 50% | ||
| Metabolism | CYP3A4 (<10%) | ||
| Elimination half-life | 12.5 hours | ||
| Excretion | 75% urine, 20% faeces | ||
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| CompTox Dashboard (EPA) | |||
| ECHA InfoCard | 100.219.080 | ||
| Chemical and physical data | |||
| Formula | C16H17N7O2S | ||
| Molar mass | 371.42 g·mol−1 | ||
| 3D model (JSmol) | |||
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Baricitinib, sold under the brand name Olumiant among others, is an immunomodulatory medication used for the treatment of rheumatoid arthritis, alopecia areata, and COVID-19. It acts as an inhibitor of janus kinase (JAK), blocking the subtypes JAK1 and JAK2.
Baricitinib is approved for medical use in the European Union and in the United States.