Drug intelligence / Profile preview

durvalumab + monalizumab + cetuximab

Development stage
Unknown
Lead developer
AstraZeneca
Modality
Monoclonal Antibodies → Antibody-Based Therapeutics
Administration
Intravenous
01

Overview

This is an investigational combination of three monoclonal antibodies: durvalumab (an anti-PD-L1 antibody developed as MEDI4736), monalizumab (an anti-NKG2A antibody, also known as IPH2201), and cetuximab (an anti-EGFR antibody, marketed as Erbitux). The combination is designed to target three distinct immune pathways and has shown anti-tumor activity in early clinical studies, particularly in solid tumors such as colorectal cancer (CRC) and recurrent or metastatic squamous cell carcinoma of the head and neck (R/M HNSCC)[1][5]. Durvalumab blocks PD-L1, enhancing T-cell mediated anti-tumor immunity; monalizumab relieves NK cells and some T cells from NKG2A-mediated inhibition, improving immune cell activation; cetuximab blocks EGFR and also triggers antibody-dependent cellular cytotoxicity (ADCC) which is further enhanced by monalizumab[2][3][5][6].

Other names
durvalumab + monalizumab + cetuximab
02

Targets

EGFR T790M (Epidermal growth factor receptor T790M mutant)KLRC1 (Killer cell lectin-like receptor subfamily C member 1)CD274 (Programmed cell death protein 1 ligand 1)

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