Ribociclib
| Clinical data | |
|---|---|
| Trade names | Kisqali |
| Other names | LEE 011 |
| AHFS/Drugs.com | Monograph |
| MedlinePlus | a617008 |
| License data |
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| Routes of administration | By mouth |
| Drug class | Antineoplastic, CDK inhibitor |
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| Pharmacokinetic data | |
| Bioavailability | Unknown |
| Protein binding | ~70% |
| Metabolism | Liver (CYP3A4) |
| Elimination half-life | 32.0 (29.7–54.7) hrs |
| Excretion | 69% feces, 23% urine |
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| CAS Number | |
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| DrugBank | |
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| CompTox Dashboard (EPA) | |
| ECHA InfoCard | 100.234.566 |
| Chemical and physical data | |
| Formula | C23H30N8O |
| Molar mass | 434.548 g·mol−1 |
| 3D model (JSmol) | |
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Ribociclib, sold under the brand name Kisqali, is a medication used for the treatment of certain kinds of breast cancer. Ribociclib is a kinase inhibitor. It was developed by Novartis and Astex Pharmaceuticals.
The most common side effects include infections, low levels of white blood cells, headache, cough, nausea (feeling sick), vomiting, diarrhea, constipation, tiredness, hair loss and rash.
Ribociclib was approved for medical use in the United States in March 2017, in the European Union in August 2017, and in the United Kingdom in February 2021.