Drug intelligence / Profile preview

dexamethasone + pegylated liposomal doxorubicin + vincristine

Development stage
Unknown
Lead developer
Johnson & Johnson
Modality
Small Molecules, Liposomes → Lipid-based Nanoparticles → Nanoparticles → Drug Delivery Systems
Administration
Intravenous, Oral
01

Overview

This drug is a combination chemotherapy regimen consisting of dexamethasone, pegylated liposomal doxorubicin, and vincristine. It is primarily used in the treatment of multiple myeloma. Pegylated liposomal doxorubicin (PLD) is a formulation of doxorubicin encapsulated in pegylated liposomes, which prolongs circulation time and reduces cardiac toxicity compared to conventional doxorubicin. Vincristine is a vinca alkaloid that inhibits microtubule formation, disrupting mitosis in cancer cells. Dexamethasone is a synthetic glucocorticoid with anti-inflammatory and immunosuppressive properties that also induces apoptosis in certain hematologic malignancies. The combination aims to maximize antitumor efficacy while minimizing toxicity; studies have shown similar response rates to traditional regimens but with reduced severe neutropenia, sepsis risk, need for central venous access, growth-factor support, and alopecia—though hand-foot syndrome may be more common due to PLD[1][2][3]. The regimen can be administered on an outpatient basis due to the pharmacokinetic advantages of PLD[5].

Brand names
DOXIL + vincristine + dexamethasone
Other names
DVd regimen
02

Targets

GR (Glucocorticoid receptor)TUBB (Tubulin (alpha and beta subunits))TOP2A (DNA topoisomerase II)

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