Drug intelligence / Profile preview

DF9001 + pembrolizumab

Development stage
Unknown
Lead developer
Dragonfly Therapeutics
Modality
Bispecific Antibodies → Multispecific Antibodies → Engineered Antibody Formats → Antibody-Based Therapeutics, Monoclonal Antibodies → Antibody-Based Therapeutics
Administration
Intravenous
01

Overview

DF9001 + pembrolizumab is an investigational combination therapy being studied primarily for advanced solid tumors expressing epidermal growth factor receptor (EGFR), including renal cell carcinoma (RCC) and head and neck squamous cell carcinoma (HNSCC). DF9001 is a first-in-class, multi-specific EGFR immune engager that redirects natural killer (NK) cells, gamma-delta T cells, and CD8 T cells toward tumor cells by engaging activating receptors NKG2D and CD16. This engagement stimulates anti-tumor immunity and induces PD-L1 expression in tumor cells, potentially sensitizing them to checkpoint inhibition. Pembrolizumab (brand name Keytruda) is an anti-PD-1 monoclonal antibody immune checkpoint inhibitor developed by Merck. The combination aims to enhance anti-tumor immune responses in EGFR-positive tumors, including those resistant to other therapies. The combination is currently being studied in a first-in-human phase 1 clinical trial, with Dragonfly Therapeutics as the sponsor and Merck as collaborator[1][2][3].

Other names
DF9001 + Keytruda
02

Targets

EGFR T790M (Epidermal growth factor receptor T790M mutant)FCGR3B (Fc gamma receptor III)PDCD1 (Programmed cell death protein 1 receptor)NKG2D (Natural killer group 2 member D receptor)

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