Drug intelligence / Profile preview

rinatabart sesutecan + bevacizumab

Development stage
Unknown
Lead developer
Genmab
Modality
Cytotoxic ADCs → Antibody-Drug Conjugates (ADCs) → Antibody Conjugates → Antibody-Based Therapeutics, Monoclonal Antibodies → Antibody-Based Therapeutics
Administration
Intravenous
01

Overview

**Rinatabart sesutecan + bevacizumab** is an investigational **combination therapy** comprised of rinatabart sesutecan (Rina-S), a folate receptor alpha (FRα)-directed antibody-drug conjugate (ADC), and bevacizumab, a monoclonal antibody targeting vascular endothelial growth factor (VEGF). Rinatabart sesutecan consists of a human monoclonal antibody targeting FRα, a hydrophilic protease-cleavable linker, and exatecan (a topoisomerase I (TOPO1) inhibitor) as the cytotoxic payload[1]. Bevacizumab inhibits angiogenesis by neutralizing VEGF-A. This combination is being tested in advanced solid tumors—particularly endometrial and ovarian cancer{1}.

Other names
rinatabart sesutecanRina-SGEN1184GEN-1184GEN 1184PRO1184PRO-1184PRO 1184bevacizumabAvastin
02

Targets

FOLR1 (FRα)VEGFA (Vascular endothelial growth factor A)TOP1 (DNA Topoisomerase I)

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