Drug intelligence / Profile preview

DSP107 + atezolizumab

Development stage
Unknown
Lead developer
KAHR Medical
Modality
Fc-Fusion Proteins → Carrier/Scaffold Proteins → Recombinant Proteins and Enzymes, Monoclonal Antibodies → Antibody-Based Therapeutics
Administration
Intravenous
01

Overview

DSP107 + atezolizumab is a combination therapy consisting of DSP107, a first-in-class bispecific fusion protein that targets both CD47 and 4-1BB, and atezolizumab, a monoclonal antibody targeting PD-L1. DSP107 is engineered to bind CD47 overexpressed on tumor cells, blocking the "don't eat me" signal to phagocytes and simultaneously presenting a 4-1BB ligand that costimulates and activates T cells. This dual mechanism aims to trigger both innate (via macrophage and polymorphonuclear leukocyte activation) and adaptive (via T-cell activation and cytotoxicity) anti-tumor immune responses. Atezolizumab further unleashes T cell activity by blocking PD-L1-mediated immune evasion, providing a synergistic immunotherapeutic approach. This combination has been tested in clinical studies in microsatellite stable metastatic colorectal cancer and other solid tumors[1][2][3][4].

Other names
DSP107 + TecentriqDSP107 + anti-PD-L1DSP107 + atezolizumab
02

Targets

TNFRSF9 (CD137 extracellular domain)CD47 (Cluster of Differentiation 47)CD274 (Programmed cell death protein 1 ligand 1)

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