Drug intelligence / Profile preview

D2C7-CAR

Development stage
Preclinical
Lead developer
Duke University
Modality
CAR-T Cells → Engineered T Cells → Adoptive Cell Transfer → Cell Therapies
Administration
Intratumoral
01

Overview

D2C7-CAR is a dual-specific chimeric antigen receptor (CAR) T-cell therapy designed to target both wild-type epidermal growth factor receptor (EGFR) and its variant III (EGFRvIII) mutation. Developed by researchers at Duke University, this cell therapy aims to address the significant intratumoral heterogeneity found in glioblastoma (GBM) and other EGFR-aberrant tumors like medulloblastoma. By utilizing the D2C7 clone, which possesses high specificity for both the overexpressed wild-type receptor and the tumor-specific vIII mutation, D2C7-CAR seeks to improve tumor clearance and prevent antigen escape mechanisms that often limit the efficacy of single-target CAR-T therapies. Preclinical studies have demonstrated robust in vitro cytotoxicity and significantly prolonged survival in orthotopic mouse models of GBM and medulloblastoma. Notably, the therapy has shown a favorable safety profile in preclinical models, with no observed cytotoxicity against EGFR-expressing human keratinocytes.

Other names
D2C7-CAR T cellsD-2C7-CAR T cellsD 2C7-CAR T cellsD2C7-targeted CAR T cellsD-2C7-targeted CAR T cellsD 2C7-targeted CAR T cells
02

Targets

Epidermal growth factor receptor (EGFR) extracellular domain D2C7 epitopeEpidermal growth factor receptor variant III and wild-type epidermal growth factor receptor shared conformational epitope

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