Drug intelligence / Profile preview

MDX-447

Development stage
Phase 1
Lead developer
Bristol Myers Squibb
Modality
Bispecific Antibodies → Multispecific Antibodies → Engineered Antibody Formats → Antibody-Based Therapeutics, Antibody Fragments → Engineered Antibody Formats → Antibody-Based Therapeutics
Administration
Intravenous, Intratumoral
01

Overview

MDX-447 is an investigational **EGFR × CD64 bispecific antibody fragment** developed through a Medarex and Merck KGaA collaboration for EGFR-expressing malignancies. It was constructed by chemically cross-linking humanized Fab fragments directed against epidermal growth factor receptor and the high-affinity immunoglobulin gamma Fc receptor I, thereby bridging EGFR-positive tumor cells to CD64-positive myeloid effector cells and promoting antibody-dependent cellular cytotoxicity and tumor-cell lysis. In a Phase 1 study in advanced solid tumors, weekly intravenous MDX-447 monotherapy had a maximum tolerated dose of 30 mg/m² but produced no objective responses; concomitant G-CSF increased toxicity and prevented meaningful dose escalation. ([link.springer.com](https://link.springer.com/content/pdf/10.1007/s002620050435.pdf))

Other names
BsAb MDX447bispecific antibody MDX447MDX447MDX-447MDX 447
02

Targets

FCGR1A (High affinity immunoglobulin gamma fc receptor I)EGFR T790M (Epidermal growth factor receptor T790M mutant)

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