Drug intelligence / Profile preview

[68Ga]-B7H3-BCH

Development stage
Unknown
Lead developer
Peking University Cancer Hospital & Institute
Modality
Antibody-Radionuclide Conjugates → Antibody Conjugates → Antibody-Based Therapeutics, Positron Emitters → Radiopharmaceuticals, Peptides
Administration
Intravenous
01

Overview

[68Ga]-B7H3-BCH (also known as [68Ga]Ga-B7H3-BCH) is a gallium-68 labeled, B7-H3 (CD276)-targeted affibody-based radiotracer developed by Peking University Cancer Hospital (Beijing Cancer Hospital). It is designed for positron emission tomography (PET) imaging to non-invasively and quantitatively map B7-H3 expression throughout the body. B7-H3 is an immune checkpoint molecule overexpressed in multiple solid tumors, including osteosarcoma, breast cancer, lung cancer, and gastric cancer, while showing low expression in normal tissues. The tracer utilizes an optimized B7-H3-targeting affibody conjugated to a chelator (such as RESCA or NOTA) and radiolabeled with gallium-68, enabling high-affinity binding and rapid clearance for high-contrast tumor visualization. It is being evaluated in clinical trials for tumor-specific diagnostics, staging, and screening of B7-H3-targeted therapies.

Other names
B7H3 Affibody-BCHB-7H3 Affibody-BCHB 7H3 Affibody-BCH[68Ga]Ga-B7H3-NOTA
02

Targets

B7-H3

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