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Brenetafusp is an ImmTAC (Immune mobilizing monoclonal TCRs Against Cancer) bispecific biologic targeting PRAME, under development for the treatment of ovarian cancer. It has shown clinical activity as monotherapy and in combination with chemotherapy in heavily pre-treated, platinum-resistant ovarian cancer patients. Bevacizumab is a recombinant humanized monoclonal antibody that inhibits vascular endothelial growth factor A (VEGF-A), thereby blocking angiogenesis and reducing tumor blood supply. Bevacizumab is approved for use in multiple cancers including colorectal, lung, glioblastoma, renal cell carcinoma, cervical cancer, and ovarian cancer. The combination of brenetafusp and bevacizumab represents a multi-modal approach targeting both tumor antigens (via T-cell redirection) and tumor vasculature (via VEGF inhibition)[3][4][5][7].
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