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DSP

Taiwan Liposome Company · FDA-approved active Small molecule

DSP is a liposomal doxorubicin formulation that delivers the chemotherapy agent doxorubicin within lipid nanoparticles to improve drug targeting and reduce systemic toxicity.

DSP is a liposomal doxorubicin formulation that delivers the chemotherapy agent doxorubicin within lipid nanoparticles to improve drug targeting and reduce systemic toxicity. Used for Metastatic breast cancer, Ovarian cancer, Multiple myeloma.

At a glance

Generic nameDSP
Also known asDexamethasone Sodium Phosphate
SponsorTaiwan Liposome Company
Drug classLiposomal anthracycline chemotherapy
TargetTopoisomerase II
ModalitySmall molecule
Therapeutic areaOncology
PhaseFDA-approved

Mechanism of action

The liposomal encapsulation of doxorubicin allows for preferential accumulation in tumor tissues through the enhanced permeability and retention (EPR) effect, while reducing exposure to healthy tissues. This formulation approach decreases cardiotoxicity and other dose-limiting side effects associated with free doxorubicin, allowing for improved therapeutic efficacy.

Approved indications

Common side effects

Key clinical trials

Primary sources

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