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dulanermin + FOLFOX + bevacizumab
- Development stage
- Unknown
- Lead developer
- Genentech
- Modality
- Nucleic Acid-Directed Small Molecules → Small Molecules, Recombinant Proteins and Enzymes, Monoclonal Antibodies → Antibody-Based Therapeutics, Covalent Small Molecules → Small Molecules, Classical Binding Small Molecules → Small Molecules
- Administration
- Intravenous
01
Overview
This is a combination regimen consisting of **dulanermin** (a recombinant human Apo2L/TRAIL that induces apoptosis in tumor cells), **FOLFOX** (a chemotherapy combination of folinic acid, fluorouracil, and oxaliplatin used primarily for colorectal cancer), and **bevacizumab** (a humanized monoclonal antibody targeting vascular endothelial growth factor A/VEGF-A, inhibiting angiogenesis). This investigational combination targets malignant cells through multiple antineoplastic mechanisms: direct apoptosis induction (dulanermin), cytotoxic chemotherapy (FOLFOX), and angiogenesis inhibition (bevacizumab). FOLFOX is most often used intravenously as cycles for 12-24 weeks in metastatic or advanced colorectal carcinoma; bevacizumab is used IV as an adjunct to chemotherapy in several cancers including colorectal cancer.
- Other names
- folinic acid + fluorouracil + oxaliplatin + dulanermin + bevacizumab
02
Targets
TNFRSF10A (Death receptor 4)TS (Thymidylate synthase)DNATNFRSF10B (DR5)VEGFA (Vascular endothelial growth factor A)
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