Acute myeloid leukaemia (AML)

Active Ingredient: Idarubicin

Indication for Idarubicin

Population group: only adults (18 years old or older)

For the treatment of acute myeloid leukaemia (AML), for remission induction in untreated patients or for remission induction in relapsed or refractory patients.

For this indication, competent medicine agencies globally authorize below treatments:

8-12 mg/m² once daily for 3-5 days

Route of admnistration


Defined daily dose

8 - 12 mg per m² of body surface area (BSA)

Dosage regimen

From 8 To 12 mg per m² of body surface area (BSA) once every day

Detailed description

12 mg/m²/day i.v. daily for 3 days in combination with cytarabine or 8 mg/m²/day i.v. daily for 5 days with/without combination.

Active ingredient


Idarubicin is a DNA intercalating anthracycline which interacts with the enzyme topoisomerase II and has an inhibitory effect on nucleic acid synthesis. Idarubicin has been shown to have a higher potency with respect to daunorubicin and to be an effective agent against murine leukaemia and lymphomas both by i.v. and oral routes.

Read more about Idarubicin

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