Drug intelligence / Profile preview

BEZ235 + paclitaxel + trastuzumab

Development stage
Unknown
Lead developer
Novartis
Modality
Monoclonal Antibodies → Antibody-Based Therapeutics, Small Molecules
Administration
Oral, Intravenous, Subcutaneous
01

Overview

This is a combination therapy consisting of three agents: BEZ235 (dactolisib), paclitaxel, and trastuzumab. BEZ235 is an orally available dual inhibitor of phosphoinositide 3-kinase (PI3K) and mammalian target of rapamycin kinase (mTOR). It inhibits the PI3K-AKT-mTOR signaling pathway, leading to reduced cancer cell viability. Paclitaxel is a chemotherapy agent that works by inhibiting microtubule disassembly, thereby blocking cell division. Trastuzumab is a monoclonal antibody targeting the human epidermal growth factor receptor 2 (HER2), commonly overexpressed in certain breast cancers. This combination has been investigated primarily for HER2-positive advanced breast cancer and other solid tumors with PI3K-pathway alterations[1][2][5]. The rationale for combining these drugs lies in their complementary mechanisms—targeting both HER2 signaling and downstream PI3K/mTOR pathways while also providing cytotoxic chemotherapy.

Brand names
Taxol (for paclitaxel)Herceptin (for trastuzumab)
Other names
NVP-BEZ235NVP-BEZ-235NVP-BEZ 235PTX (for paclitaxel, as used in clinical trials)TZ (for trastuzumab, as used in clinical trials)
02

Targets

TUBB (Tubulin (alpha and beta subunits))PI3K (Phosphoinositide-3-kinase regulatory subunit 6)ERBB2 (Erb-b2 receptor tyrosine kinase 2)mTOR (Mammalian target of rapamycin kinase)

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