OncoMatch/Clinical Trials/JS207
JS207 (JS207) Clinical Trials
JS207 is a recombinant humanized anti-PD-1/VEGF bispecific antibody developed by Junshi Biosciences, designed to simultaneously block the PD-1/PD-L1 axis and inhibit VEGF-driven angiogenesis with VEGF-binding affinity designed to be comparable to bevacizumab. With numerous ongoing Phase 2 studies, JS207 is being evaluated in NSCLC (including neoadjuvant settings for resectable disease), colorectal cancer, triple-negative breast cancer, and hepatocellular carcinoma, both as monotherapy and in combination with chemotherapy, checkpoint antibodies, and ADCs. Junshi filed an IND with FDA clearance for a Phase 2/3 study comparing JS207 to nivolumab for neoadjuvant treatment of resectable AGA-negative NSCLC. Eligibility criteria vary by indication and arm; most NSCLC trials specify actionable genomic alteration (AGA) status — meaning whether a known targetable mutation such as EGFR, ALK, or ROS1 is present — and some specify PD-L1 expression thresholds (perioperative and neoadjuvant trials may not).
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Recruiting JS207 trials
Ranked by phase and US site count.
Fudan University Shanghai Cancer Center Breast Cancer Precision Platform Series Study- Neoadjuvant Therapy
Fudan University
JS207 Combined With JS007 as First-line Treatment for Advanced Hepatocellular Carcinoma
Shanghai Junshi Bioscience Co., Ltd.
JS207Combined With Chemotherapy in First-line Treatment of Advanced NSCLC
Shanghai Junshi Bioscience Co., Ltd.
How OncoMatch helps you find JS207 trials
AI reads the protocol
OncoMatch reads the eligibility criteria for every JS207 trial and extracts structured requirements — biomarkers, stage, prior therapy — from protocol text.
Enter your results
Select your cancer type and mark your biomarker results. Your data never leaves your device. OncoMatch instantly filters to trials you may qualify for.
See your matches
Each trial shows which criteria you meet, which you don't, and which need more information. Bring the shortlist to your oncologist.