Drug intelligence / Profile preview

Non-pegylated liposomal doxorubicin + trastuzumab + docetaxel

Development stage
Unknown
Lead developer
Chiesi
Modality
Small Molecules, Liposomes → Lipid-based Nanoparticles → Nanoparticles → Drug Delivery Systems, Monoclonal Antibodies → Antibody-Based Therapeutics
Administration
Intravenous
01

Overview

A combination regimen consisting of non-pegylated liposomal doxorubicin, trastuzumab, and docetaxel is used as first-line therapy in patients with metastatic breast cancer that overexpresses human epidermal growth factor receptor 2 (HER2). Non-pegylated liposomal doxorubicin is an anthracycline antibiotic formulated in a liposome to reduce cardiotoxicity compared to conventional formulations. Trastuzumab is a monoclonal antibody targeting the HER2 receptor, inhibiting proliferation of tumor cells that overexpress this protein. Docetaxel is a taxane-class chemotherapeutic agent that promotes microtubule assembly and inhibits cell division. The combination leverages different mechanisms of action for synergistic antitumor activity while aiming to minimize overlapping toxicities, particularly cardiac toxicity associated with anthracyclines and trastuzumab. Clinical studies have shown promising response rates and manageable safety profiles for this regimen in HER2-positive metastatic breast cancer[8].

Brand names
Herceptin + Taxotere + Myocet
Other names
trastuzumab + docetaxel + liposomal doxorubicintrastuzumab/docetaxel/NPLD
02

Targets

TUBB (Tubulin (alpha and beta subunits))TOP2A (DNA topoisomerase II)ERBB2 (Erb-b2 receptor tyrosine kinase 2)

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