Drug intelligence / Profile preview

211At-MX35 F(ab')2

Development stage
Unknown
Lead developer
Memorial Sloan Kettering Cancer Center
Modality
Antibody-Radionuclide Conjugates → Antibody Conjugates → Antibody-Based Therapeutics, Antibody Fragments → Engineered Antibody Formats → Antibody-Based Therapeutics
Administration
Intraperitoneal
01

Overview

211At-MX35 F(ab')2 is a radiolabeled monoclonal antibody fragment designed for targeted alpha-particle therapy, specifically for ovarian cancer. It comprises the murine IgG1-class monoclonal antibody MX35 (fragment F(ab')2), which binds to a cell-surface glycoprotein (95 kDa) that is highly expressed in approximately 90% of human epithelial ovarian cancers (OVCAR-3 cells). The antibody is labeled with astatine-211 (^211At), an alpha-emitting radionuclide, which enables localized delivery of cytotoxic radiation to microscopic tumor clusters while minimizing exposure to healthy tissue. The drug is administered intraperitoneally, allowing direct contact with residual cancer cells after chemotherapy. Developed at Memorial Sloan-Kettering Cancer Center, its clinical application is currently under investigation in open clinical trials in Denmark and Sweden, mainly focusing on safety, pharmacokinetics, and toxicity in relapsed or recurrent ovarian cancer[1][2][3][4][5].

Other names
211-astatine-MX35 F(ab')2At-211-MX35-F(ab')2Astatine-211-MX35-F(ab')2
02

Targets

SLC34A2 (Sodium-dependent phosphate transporter type IIb)

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