Drug intelligence / Profile preview

trastuzumab + docetaxel + NPLD + bevacizumab

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

Overview

This is a combination regimen consisting of four drugs: trastuzumab, docetaxel, nonpegylated liposomal doxorubicin (NPLD), and bevacizumab. Trastuzumab is a monoclonal antibody targeting the human epidermal growth factor receptor 2 (HER2), used primarily in HER2-positive breast cancer. Docetaxel is a taxane-class small molecule chemotherapeutic that inhibits microtubule depolymerization, disrupting cell division. NPLD (nonpegylated liposomal doxorubicin) is an anthracycline antibiotic encapsulated in liposomes to reduce cardiotoxicity while intercalating DNA and inhibiting topoisomerase II. Bevacizumab is a monoclonal antibody that binds vascular endothelial growth factor A (VEGF-A), inhibiting angiogenesis. This combination has been studied for efficacy and safety in HER2-positive metastatic or early-stage breast cancer, with particular attention to cardiac toxicity due to the inclusion of both anthracyclines and anti-HER2 therapy[1][4][6].

Brand names
Caelyx
Other names
pegylated liposomal doxorubicin
02

Targets

TUBB (Tubulin (alpha and beta subunits))ERBB2 (Erb-b2 receptor tyrosine kinase 2)TOP2A (DNA topoisomerase II)VEGFA (Vascular endothelial growth factor A)DNA

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