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gemcitabine + oxaliplatin
- Development stage
- Phase 3
- Lead developer
- Eli Lilly
- Modality
- Orthosteric Ligands → Classical Binding Small Molecules → Small Molecules, DNA Intercalators/Alkylators → Nucleic Acid-Directed Small Molecules → Small Molecules, Metabolically Activated Prodrugs → Prodrugs/Conditional Activator Small Molecules → Small Molecules
- Administration
- Intravenous
01
Overview
Gemcitabine + oxaliplatin is a combination chemotherapy regimen widely used for the treatment of various advanced solid tumors, including non-small cell lung cancer, gallbladder cancer, urothelial carcinoma, and others. Gemcitabine is a synthetic pyrimidine nucleoside analog that inhibits DNA synthesis by being incorporated into DNA during replication and causing chain termination. Oxaliplatin is a third-generation platinum-based compound that forms crosslinks with DNA, inhibiting its replication and transcription and inducing apoptosis in tumor cells. The two drugs have distinct mechanisms of action but are both broad-spectrum cytotoxic agents; their toxicities do not overlap significantly, making the combination synergistic for antitumor activity[2][1][5]. This regimen is administered intravenously.
- Other names
- 吉西他滨 + 奥沙利铂GemOx
02
Targets
DNADNA polymerase family
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