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Liposomal daunorubicin

University of Birmingham · Phase 3 active Small molecule

Liposomal daunorubicin is an anthracycline chemotherapy agent encapsulated in liposomes that intercalates into DNA and inhibits topoisomerase II, leading to DNA damage and cancer cell death.

Liposomal daunorubicin is an anthracycline chemotherapy agent encapsulated in liposomes that intercalates into DNA and inhibits topoisomerase II, leading to DNA damage and cancer cell death. Used for Acute myeloid leukemia (AML), Acute lymphoblastic leukemia (ALL).

At a glance

Generic nameLiposomal daunorubicin
Also known asDaunoxome, DaunoXome, daunorubicin liposomal, liposomal daunorubicin
SponsorUniversity of Birmingham
Drug classAnthracycline chemotherapy agent
TargetTopoisomerase II, DNA
ModalitySmall molecule
Therapeutic areaOncology
PhasePhase 3

Mechanism of action

Daunorubicin is a topoisomerase II inhibitor that intercalates between DNA base pairs, preventing DNA replication and transcription. The liposomal formulation encapsulates the drug in lipid vesicles, which improves pharmacokinetics, reduces systemic toxicity, and enhances delivery to tumor tissues. This formulation allows for higher doses with potentially improved therapeutic index compared to conventional daunorubicin.

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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