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Cytarabine vs. Cytarabine+Amsacrine+Mitoxantrone

Technische Universität Dresden · FDA-approved active Small molecule

Cytarabine is a cytidine analog that inhibits DNA synthesis, while the combination with amsacrine and mitoxantrone adds topoisomerase II inhibition and intercalating DNA damage to enhance leukemic cell killing.

Cytarabine is a cytidine analog that inhibits DNA synthesis, while the combination with amsacrine and mitoxantrone adds topoisomerase II inhibition and intercalating DNA damage to enhance leukemic cell killing. Used for Acute myeloid leukemia (AML), particularly in relapsed or refractory disease.

At a glance

Generic nameCytarabine vs. Cytarabine+Amsacrine+Mitoxantrone
SponsorTechnische Universität Dresden
Drug classCombination chemotherapy (nucleoside analog + topoisomerase II inhibitors)
TargetDNA polymerase (cytarabine); Topoisomerase II (amsacrine, mitoxantrone)
ModalitySmall molecule
Therapeutic areaOncology
PhaseFDA-approved

Mechanism of action

Cytarabine (ara-C) is a nucleoside analog that is phosphorylated intracellularly and incorporated into DNA, inhibiting DNA polymerase and causing chain termination. Amsacrine and mitoxantrone are topoisomerase II inhibitors that intercalate into DNA and prevent religation of DNA strands, leading to double-strand breaks. The combination therapy targets multiple mechanisms of DNA damage to overcome resistance in acute myeloid leukemia.

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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