Drug intelligence / Profile preview

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

Development stage
Phase 1
Lead developer
Hansoh Pharmaceutical Group
Modality
Cytotoxic ADCs → Antibody-Drug Conjugates (ADCs) → Antibody Conjugates → Antibody-Based Therapeutics, Monoclonal Antibodies → Antibody-Based Therapeutics, Small Molecules
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

B7-H3DNATS (Thymidylate synthase)VEGFA (Vascular endothelial growth factor A)

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