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LDAC and/or Mitoxantrone

DKMS gemeinnützige GmbH · Phase 3 active Small molecule

LDAC (low-dose cytarabine) and mitoxantrone are chemotherapy agents that inhibit DNA synthesis and topoisomerase II, respectively, to kill rapidly dividing leukemic cells.

LDAC (low-dose cytarabine) and mitoxantrone are chemotherapy agents that inhibit DNA synthesis and topoisomerase II, respectively, to kill rapidly dividing leukemic cells. Used for Acute myeloid leukemia (AML), particularly in elderly or unfit patients, Relapsed or refractory acute leukemia.

At a glance

Generic nameLDAC and/or Mitoxantrone
SponsorDKMS gemeinnützige GmbH
Drug classChemotherapy combination (nucleoside analog + topoisomerase II inhibitor)
TargetDNA polymerase (cytarabine); Topoisomerase II (mitoxantrone)
ModalitySmall molecule
Therapeutic areaOncology
PhasePhase 3

Mechanism of action

Low-dose cytarabine is a nucleoside analog that incorporates into DNA and inhibits DNA polymerase, while mitoxantrone is a topoisomerase II inhibitor that causes DNA strand breaks. Together, they are used in combination chemotherapy regimens to treat acute myeloid leukemia and other hematologic malignancies by inducing apoptosis in leukemic blasts.

Approved indications

Common side effects

Key clinical trials

Primary sources

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SourceUsed for
ClinicalTrials.govTrial enrolment, design, endpoints, results

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