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Liposome doxorubicin

Sun Yat-sen University · FDA-approved active Small molecule

Liposome-encapsulated doxorubicin delivers the chemotherapy agent doxorubicin to cancer cells while reducing exposure to healthy tissues, thereby improving tolerability.

Liposome-encapsulated doxorubicin delivers the chemotherapy agent doxorubicin to cancer cells while reducing exposure to healthy tissues, thereby improving tolerability. Used for Metastatic breast cancer, Ovarian cancer, Multiple myeloma.

At a glance

Generic nameLiposome doxorubicin
Also known asliposome adriamycin, Caelyx
SponsorSun Yat-sen University
Drug classLiposomal chemotherapy; topoisomerase II inhibitor
TargetDNA topoisomerase II
ModalitySmall molecule
Therapeutic areaOncology
PhaseFDA-approved

Mechanism of action

Doxorubicin is a topoisomerase II inhibitor that intercalates into DNA and prevents DNA replication in rapidly dividing cells. By encapsulating doxorubicin in liposomes, the formulation preferentially accumulates in tumor tissues through the enhanced permeability and retention (EPR) effect, reducing cardiotoxicity and other systemic toxicities associated with free doxorubicin while maintaining anti-tumor efficacy.

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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