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gemcitabine + cisplatin + nimotuzumab + sintilimab

Development stage
Unknown
Lead developer
Eli Lilly
Modality
Monoclonal Antibodies → Antibody-Based Therapeutics, Small Molecules
Administration
Intravenous
01

Overview

This drug is a **combination regimen** consisting of **gemcitabine** and **cisplatin** (commonly referred to as the "GP regimen"), in combination with **nimotuzumab**, a recombinant humanized monoclonal antibody targeting the epidermal growth factor receptor (EGFR), and **sintilimab**, a monoclonal antibody that acts as a PD-1 checkpoint inhibitor. This combination targets tumor cells through synergistic mechanisms: the GP regimen delivers cytotoxic chemotherapy, nimotuzumab disrupts EGFR-mediated signaling and enhances sensitivity to therapy, and sintilimab activates immune-mediated anti-tumor responses by blocking PD-1/PD-L1 immune checkpoints. Regimens of this type are being evaluated in clinical studies for advanced solid tumors, especially nasopharyngeal carcinoma and esophageal cancer[1][4][8]. Main mechanisms include inhibition of DNA synthesis and repair (gemcitabine), DNA crosslinking (cisplatin), EGFR pathway blockade (nimotuzumab), and enhanced anti-tumor immunity via immune checkpoint inhibition (sintilimab).

Other names
GP Regimen + nimotuzumab + sintilimab
02

Targets

DNA polymerase familyDNAPDCD1 (Programmed cell death protein 1 receptor)EGFR T790M (Epidermal growth factor receptor T790M mutant)

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