Drug intelligence / Profile preview

JS207 + capecitabine + oxaliplatin

Development stage
Phase 2
Lead developer
Junshi Biosciences
Modality
Bispecific Antibodies → Multispecific Antibodies → Engineered Antibody Formats → Antibody-Based Therapeutics, Small Molecules
Administration
Intravenous, Oral
01

Overview

JS207 + capecitabine + oxaliplatin is an investigational combination regimen consisting of JS207, a recombinant humanized bispecific antibody targeting programmed cell death protein 1 (PD-1) and vascular endothelial growth factor A (VEGFA), combined with the standard XELOX (CAPOX) chemotherapy backbone (capecitabine and oxaliplatin). Developed by Junshi Biosciences, JS207 simultaneously blocks the PD-1/PD-L1/PD-L2 immune checkpoint pathways and inhibits VEGF-mediated tumor angiogenesis, thereby enhancing immune cell infiltration and improving the tumor microenvironment. Capecitabine, an oral fluoropyrimidine carbamate prodrug, and oxaliplatin, a platinum-based DNA alkylating agent, provide synergistic cytotoxic activity. This combination is currently being evaluated in Phase 2 clinical trials (such as NCT06885385) as a first-line treatment for patients with mismatch repair proficient/microsatellite stable (pMMR/MSS) metastatic colorectal cancer (mCRC).

Other names
JS207 + CAPOXJS207 + XELOXJS207 plus CAPOXJS-207 plus CAPOXJS 207 plus CAPOXJS207 plus capecitabine and oxaliplatinJS-207 plus capecitabine and oxaliplatinJS 207 plus capecitabine and oxaliplatinJS207 plus XELOXJS-207 plus XELOXJS 207 plus XELOX
02

Targets

DNAPDCD1 (Programmed cell death protein 1 receptor)CD274 (Programmed cell death protein 1 ligand 1)PDCD1LG2 (Programmed cell death 1 ligand 2)TS (Thymidylate synthase)VEGFA (Vascular endothelial growth factor A)VEGFR2 (Vascular endothelial growth factor receptor 2)

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