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Pronunciation | /ˌtraɪləˈsaɪklɪb/ TRY-lə-SY-klib |
Trade names | Cosela |
AHFS/Drugs.com | FDA Professional Drug Information |
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Routes of administration | Intravenous |
Drug class | Cyclin-dependent kinase (CDK) inhibitor |
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Formula | C24H30N8O |
Molar mass | 446.559 g·mol−1 |
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Trilaciclib, sold under the brand name Cosela, is a medication used to reduce the frequency of chemotherapy-induced bone marrow suppression.[1][2][3][4]
The most common side effects include fatigue; low levels of calcium, potassium and phosphate; increased levels of an enzyme called aspartate aminotransferase; headache; and infection in the lungs (pneumonia).[2]
Trilaciclib may help protect bone marrow cells from damage caused by chemotherapy by inhibiting cyclin-dependent kinase 4/6, a type of enzyme.[2] Trilaciclib is the first therapy in its class and was approved for medical use in the United States in February 2021.[2][5] The U.S. Food and Drug Administration considers it to be a first-in-class medication.[6]
Chemotherapy drugs are designed to kill cancer cells but can damage normal tissues as well.[2] The bone marrow is particularly susceptible to chemotherapy damage.[2] The bone marrow makes red blood cells, white blood cells, and platelets (small fragments in the blood) that transport oxygen, fight infection, and stop bleeding.[2] When damaged, the bone marrow produces fewer of these cells, leading to fatigue, increased risk of infection, and bleeding, among other problems.[2] Trilaciclib may help protect the normal bone marrow cells from the harmful effects of chemotherapy.[2]