Drug intelligence / Profile preview

64Cu-TE2A-9E7.4

Development stage
Unknown
Modality
Antibody-Radionuclide Conjugates → Antibody Conjugates → Antibody-Based Therapeutics
Administration
Intravenous
01

Overview

64Cu-TE2A-9E7.4 is a radiolabeled monoclonal antibody used for immuno-positron emission tomography (immuno-PET) imaging, specifically targeting CD138 (syndecan-1), a cell surface antigen highly expressed in multiple myeloma cells. The drug consists of the murine anti-CD138 antibody 9E7.4 conjugated to the chelator TE2A and radiolabeled with copper-64 (^64Cu). Its mechanism relies on the antibody's specific binding to CD138 on myeloma cells, enabling sensitive in vivo detection of myeloma lesions. Compared to 18F-FDG and [^64Cu]CuCl2 PET tracers, 64Cu-TE2A-9E7.4 has demonstrated improved tumor uptake, higher tumor-to-background ratios, and superior lesion detection in preclinical murine models of multiple myeloma. Its immunoreactivity remains high following radiolabeling, making it a promising candidate for specific and sensitive PET imaging of multiple myeloma[1][2][3][5][6][7].

Other names
64Cu-labeled 9E7.4copper-64 anti-CD138 9E7.4copper64 anti-CD138 9E7.4copper 64 anti-CD138 9E7.464Cu-anti-CD13864Cu-TE2A-anti-CD138
02

Targets

SDC1 (Syndecan-1)

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