Prognia
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🇪🇺EU · EMAAuthorisedATC: L01BC08

Dacogen(decitabine)

Leukemia, Myeloid

Marketing Authorisation Holder: Janssen-Cilag International N.V.

EMA Authorisation: 20/09/2012

INN: decitabine

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.

Official EMA Resources

View on EMA (ema.europa.eu)

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Medical disclaimer: This information is intended for qualified healthcare professionals. Always verify with the official EMA Summary of Product Characteristics (SmPC) before clinical use.