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PLD

AGO Research GmbH · FDA-approved active Small molecule

PLD is a pegylated liposomal doxorubicin that delivers the chemotherapy agent doxorubicin within lipid nanoparticles to reduce systemic toxicity while maintaining anti-tumor efficacy.

PLD is a pegylated liposomal doxorubicin that delivers the chemotherapy agent doxorubicin within lipid nanoparticles to reduce systemic toxicity while maintaining anti-tumor efficacy. Used for Ovarian cancer, Breast cancer, Multiple myeloma.

At a glance

Generic namePLD
Also known asdoxorubicin, caelyx, duomeisu, DOXIL, Caelyx, ATI-0918, doxorubicin hydrochloride liposome
SponsorAGO Research GmbH
Drug classPegylated liposomal chemotherapy
TargetDNA (topoisomerase II inhibitor via doxorubicin)
ModalitySmall molecule
Therapeutic areaOncology
PhaseFDA-approved

Mechanism of action

The drug encapsulates doxorubicin in pegylated liposomes, which preferentially accumulate in tumor tissue through the enhanced permeability and retention (EPR) effect. This formulation reduces cardiotoxicity and other systemic side effects associated with free doxorubicin while preserving its DNA intercalation and topoisomerase II inhibition mechanisms. The pegylation extends circulation time and improves tumor targeting.

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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