Drug intelligence / Profile preview

cytarabine + daunorubicin liposome

Development stage
Phase 4
Lead developer
Jazz Pharmaceuticals
Modality
Small Molecules, Lipid-based Nanoparticles → Nanoparticles → Drug Delivery Systems
Administration
Intravenous
01

Overview

CPX-351 (Vyxeos) is a liposomal nanoparticle formulation that co-encapsulates two conventional chemotherapy agents, cytarabine and daunorubicin, in a fixed 5:1 molar ratio. This specific ratio has been shown in preclinical models to be synergistic in killing leukemia cells. The liposomal delivery system is designed to prolong the half-life of the drugs in the plasma and preferentially accumulate in the bone marrow, where it is taken up by leukemia cells. Once internalized, the liposomes release the drugs, which then exert their cytotoxic effects: cytarabine inhibits DNA polymerase and DNA synthesis, while daunorubicin intercalates into DNA and inhibits topoisomerase II. CPX-351 is primarily indicated for the treatment of adults with newly-diagnosed therapy-related acute myeloid leukemia (t-AML) or AML with myelodysplasia-related changes (AML-MRC). It was originally developed by Celator Pharmaceuticals, which was subsequently acquired by Jazz Pharmaceuticals.

Brand names
Vyxeos
Other names
Vyxeos LiposomalLiposomal cytarabine-daunorubicinLiposomal daunorubicin-cytarabine
02

Targets

DNADNA polymerase familyTOP2A (DNA topoisomerase II)

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