Decitabine/cedazuridine, sold under the brand name Inqovi, is a fixed-dose combination anticancer medication used to treat myelodysplastic syndromes and chronic myelomonocytic leukemia in adults. Decitabine is a nucleoside metabolic inhibitor that disrupts the growth of abnormal blood cells, and cedazuridine is a cytidine deaminase inhibitor that protects decitabine from being broken down in the gut, allowing the combination to be taken as an oral tablet rather than by injection. Myelodysplastic syndromes are a group of blood cancers in which the bone marrow produces defective blood cells, leading to low counts of one or more blood cell types. The United States Food and Drug Administration approved the combination in July 2020, and the European Union approved it in September 2023. It is marketed by Astex Pharmaceuticals, Inc., a subsidiary of Otsuka Pharmaceutical Co. Ltd.
Facts
Classification
Approval Status ATC ClassSourced to the subject's own accountL: Antineoplastic and Immunomodulating Agents 2 Route of Administration First Approved / Isolated Year Sources
1. Decitabine/cedazuridine (Wikipedia)
Lead section, approval-status statement
Decitabine/cedazuridine was approved for medical use in the United States and Canada in July 2020, and in the European Union in September 2023.
Lead section, route-of-administration statement
It is taken by mouth.
View the Source2. Anatomical Therapeutic Chemical Classification System (Wikipedia)
WikipediaFirst-level anatomical group codes, Code LQuote, First-level anatomical group codes, Code L
Antineoplastic and immunomodulating agents
View the Source 3. Drugs.com: Inqovi (decitabine and cedazuridine) FDA Approval History
FDA Approval HistoryQuote, FDA Approval History
Inqovi was first approved by the FDA on July 7, 2020
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