Drug intelligence / Profile preview

anti-EGFR-IL-dox

Development stage
Discontinued
Lead developer
Swiss Group for Clinical Cancer Research
Modality
Lipid-based Nanoparticles → Nanoparticles → Drug Delivery Systems, Antibody Fragments → Engineered Antibody Formats → Antibody-Based Therapeutics
Administration
Intravenous
01

Overview

anti-EGFR-IL-dox is a targeted nanomedicine consisting of pegylated liposomes containing the cytotoxic agent doxorubicin. The liposomal surface is functionalized with Fab' fragments of the anti-EGFR monoclonal antibody cetuximab, allowing for specific targeting of cells expressing the epidermal growth factor receptor (EGFR). Developed by the Swiss Group for Clinical Cancer Research (SAKK) with support from Merrimack Pharmaceuticals, it was primarily investigated as a first-line treatment for advanced triple-negative breast cancer (TNBC). The drug is designed to improve the therapeutic index of doxorubicin by concentrating the drug within EGFR-positive tumor cells through receptor-mediated endocytosis. Although the formulation demonstrated a favorable safety profile and was well-tolerated in clinical trials, it failed to meet primary efficacy endpoints in a multicenter Phase II study (SAKK 24/14) for TNBC, leading to the conclusion that it should not be further developed for this specific indication.

Other names
anti-EGFR immunoliposomes loaded with doxorubicindoxorubicin-loaded anti-EGFR immunoliposomesanti-EGFR-ILs-doxorubicin
02

Targets

EGFR T790M (Epidermal growth factor receptor T790M mutant)TOP2A (DNA topoisomerase II)DNA

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