Drug intelligence / Profile preview

HS-20093 + bevacizumab + oxaliplatin + 5-fluorouracil + leucovorin

Development stage
Unknown
Lead developer
Hansoh Pharmaceutical Group
Modality
Small Molecules, Cytotoxic ADCs → Antibody-Drug Conjugates (ADCs) → Antibody Conjugates → Antibody-Based Therapeutics, Monoclonal Antibodies → Antibody-Based Therapeutics
Administration
Intravenous
01

Overview

This is a combination regimen consisting of: - **HS-20093**: a fully humanized IgG1 antibody-drug conjugate (ADC) targeting B7-H3, overexpressed on solid tumor cells, with a mechanism involving targeted cytotoxic delivery[1][3][5][7]; - **bevacizumab**: a humanized monoclonal antibody that inhibits vascular endothelial growth factor A (VEGF-A), blocking angiogenesis[2][4][8]; - **oxaliplatin**: a platinum-based chemotherapeutic causing DNA crosslinking and apoptosis in rapidly dividing cells; - **5-fluorouracil**: a pyrimidine antimetabolite that inhibits thymidylate synthase, disrupting DNA synthesis; - **leucovorin**: a reduced folate used to enhance the effects of 5-fluorouracil. This regimen is primarily investigated for advanced solid tumors, including small cell lung cancer and potentially other indications, leveraging cytotoxic, antiangiogenic, and targeted mechanisms.

02

Targets

TS (Thymidylate synthase)VEGFA (Vascular endothelial growth factor A)TOP1 (DNA Topoisomerase I)B7-H3DNA

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