Drug intelligence / Profile preview

tidapaxicept

Development stage
Unknown
Lead developer
ImmuneOnco
Modality
Fc-Fusion Proteins → Carrier/Scaffold Proteins → Recombinant Proteins and Enzymes
Administration
Intravenous
01

Overview

Tidapaxicept (IMM01) is a recombinant human SIRPα-IgG1 Fc fusion protein designed to target the CD47-SIRPα pathway. Developed by ImmuneOnco Biopharmaceuticals, it acts as a CD47 antagonist, blocking the "don't eat me" signal that tumor cells use to evade the immune system. By inhibiting the interaction between CD47 on cancer cells and SIRPα on macrophages, tidapaxicept promotes macrophage-mediated phagocytosis. A distinguishing feature of tidapaxicept is its engineered lack of binding to human erythrocytes, which minimizes the risk of hemagglutination and anemia, common toxicities associated with other CD47-targeting agents. It is currently being evaluated in Phase 3 clinical trials for PD-(L)1-refractory classical Hodgkin lymphoma and in Phase 2 trials for various other hematological malignancies and solid tumors.

Other names
tidapaxiceptSIRPα-Fc fusion protein
02

Targets

CD47 (Cluster of Differentiation 47)FcγR (Low affinity immunoglobulin gamma Fc region receptor II-c)

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