Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
This drug combination consists of envafolimab, a subcutaneously administered PD-L1 immune checkpoint inhibitor; chemotherapy agents (commonly platinum-based doublet chemotherapy); and recombinant human endostatin (Endostar), an anti-angiogenic agent. Envafolimab works by blocking the PD-L1 protein on tumor cells to enhance immune system recognition and destruction of cancer cells. Recombinant human endostatin inhibits angiogenesis by binding to VEGF receptor 2 (VEGF-R2), suppressing vascular endothelial tube formation and normalizing tumor vasculature, which can improve delivery of cytotoxic agents. Chemotherapy acts through cytotoxic mechanisms to kill rapidly dividing cancer cells. The combination is being investigated primarily for advanced non-small cell lung cancer (NSCLC) without driver mutations as a first-line treatment option. This regimen aims to improve efficacy while maintaining tolerability compared with standard chemo-immunotherapy regimens alone.
Beyond the preview
Explore the evidence, development activity, and competitive landscape with Gosset’s full data platform.
Follow clinical development from study design and recruitment through results.
Explore development by indication, patient population, and geography.
Trace asset ownership, licensing agreements, and commercial partnerships.
Explore the patent landscape and regulatory exclusivity around an asset.
Compare development programs by target, modality, and indication.
Connect source evidence and development news to your research questions.
See how Gosset can support your research on envafolimab + chemotherapy + recombinant human endostatin.