Indication
Treatment of adult patients with newly diagnosed de novo or secondary acute myeloid leukaemia (AML), according to the World Health Organization (WHO) classification, who are not candidates for standard induction chemotherapy.
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Leukemia, Myeloid
Marketing Authorisation Holder: Janssen-Cilag International N.V.
EMA Authorisation: 20/09/2012
INN: decitabine
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Ask Osler about Dacogen: drug interactions and guideline evidence, with every claim numbered to its source. For reference and learning, not treatment advice.
Medical disclaimer: This information is intended for qualified healthcare professionals. Always verify with the official EMA Summary of Product Characteristics (SmPC) before clinical use.