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matuzumab + epirubicin + cisplatin + capecitabine

Development stage
Phase 2
Lead developer
Merck KGaA
Modality
Monoclonal Antibodies → Antibody-Based Therapeutics, Small Molecules
Administration
Intravenous, Oral
01

Overview

This is a **combination therapy** comprising four drugs: **matuzumab**, a humanized IgG1 monoclonal antibody targeting epidermal growth factor receptor (**EGFR**), with **epirubicin** (an anthracycline topoisomerase II inhibitor), **cisplatin** (a platinum-based DNA crosslinker), and **capecitabine** (a prodrug of 5-fluorouracil). It was studied as first-line treatment for advanced, EGFR-positive oesophagogastric adenocarcinoma. Matuzumab blocks ligands from binding to EGFR, thereby inhibiting receptor-mediated downstream signaling and tumor cell proliferation; it can also trigger antibody-dependent cytotoxicity. The other three components are established chemotherapy agents with cytotoxic antitumor properties.

Other names
matuzumab + ECX
02

Targets

DNAEGFR (Epidermal growth factor receptor)TS (Thymidylate synthase)TOP2A (DNA topoisomerase II)

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