Drug intelligence / Profile preview

SYS6090 + bevacizumab + FOLFOXIRI

Development stage
Phase 2
Lead developer
Suzhou Xinnuowei Pharmaceutical Technology
Modality
Monoclonal Antibodies → Antibody-Based Therapeutics, Small Molecules
Administration
Intravenous
01

Overview

SYS6090 + bevacizumab + FOLFOXIRI is an investigational combination therapy regimen being developed by CSPC Megalith Biopharmaceutical for the treatment of advanced or metastatic colorectal cancer. The regimen combines SYS6090, a recombinant humanized monoclonal antibody targeting the programmed cell death protein 1 (PD-1) receptor, with bevacizumab, an anti-angiogenic monoclonal antibody targeting vascular endothelial growth factor (VEGF), and the FOLFOXIRI chemotherapy backbone (comprising fluorouracil, leucovorin, oxaliplatin, and irinotecan). This intensive combination is primarily being evaluated in patients with proficient mismatch repair/microsatellite stable (pMMR/MSS) colorectal cancer, a population that has historically shown limited response to single-agent immune checkpoint inhibitors. The rationale for this approach is to utilize the cytotoxic and anti-angiogenic effects of chemotherapy and bevacizumab to potentially sensitize the tumor microenvironment to PD-1 blockade, thereby improving therapeutic efficacy.

Other names
SYS6090 + bevacizumab + fluorouracil + leucovorin + oxaliplatin + irinotecan
02

Targets

IL-15R (Interleukin 15 receptor alpha/interleukin 15 complex)PDCD1 (Programmed cell death protein 1 receptor)TOP1 (DNA Topoisomerase I)VEGFA (Vascular endothelial growth factor A)DNATS (Thymidylate synthase)

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