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Drugs and Medicinal Substances

Decitabine/cedazuridine

Antineoplastic and Immunomodulating Agents

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
Approved 1
ATC ClassSourced to the subject's own account
L: Antineoplastic and Immunomodulating Agents 2
Route of Administration
Oral 1
First Approved / Isolated Year
2020 3
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.
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2. Anatomical Therapeutic Chemical Classification System (Wikipedia)
WikipediaFirst-level anatomical group codes, Code L
Quote, First-level anatomical group codes, Code L
Antineoplastic and immunomodulating agents
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3. Drugs.com: Inqovi (decitabine and cedazuridine) FDA Approval History
FDA Approval History
Quote, FDA Approval History
Inqovi was first approved by the FDA on July 7, 2020
View the Source
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