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anti-EGFR immunoliposomes loaded with doxorubicin

Development stage
Phase 2
Lead developer
University Hospital Basel
Modality
Small Molecules, Antibody Fragments → Engineered Antibody Formats → Antibody-Based Therapeutics, Liposomes → Lipid-based Nanoparticles → Nanoparticles → Drug Delivery Systems, Cytotoxic ADCs → Antibody-Drug Conjugates (ADCs) → Antibody Conjugates → Antibody-Based Therapeutics
Administration
Intravenous
01

Overview

Anti-EGFR immunoliposomes loaded with doxorubicin are a targeted nanomedicine designed for the treatment of cancers that overexpress the epidermal growth factor receptor (EGFR). This formulation consists of pegylated liposomes encapsulating the chemotherapeutic agent doxorubicin. The surface of these liposomes is functionalized with antibody fragments derived from cetuximab (C225), which specifically bind to EGFR on tumor cells. Upon binding, the immunoliposome is internalized by EGFR-expressing cancer cells, enabling intracellular release of doxorubicin and enhancing cytotoxicity while aiming to reduce off-target toxicity. The drug has been evaluated in phase I and II clinical trials for advanced solid tumors and triple-negative breast cancer (TNBC) expressing EGFR[2][5][8]. It has also been studied in relapsed or refractory high-grade gliomas[1][6]. While early-phase studies showed manageable toxicity and some efficacy signals, a phase II trial in TNBC did not meet its primary endpoint for progression-free survival at 12 months[2][8].

Other names
doxorubicin-loaded anti-EGFR immunoliposomesIL-C225IL-C-225IL-C 225DXR-IL-C225DXR-IL-C-225DXR-IL-C 225
02

Targets

EGFR T790M (Epidermal growth factor receptor T790M mutant)DNA

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