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liposomal irinotecan + sintilimab + anlotinib
- Development stage
- Phase 2
- Lead developer
- Sun Yat-Sen Memorial Hospital
- Modality
- Monoclonal Antibodies → Antibody-Based Therapeutics, Small Molecules, Nanoparticles → Drug Delivery Systems
- Administration
- Intravenous, Oral
01
Overview
liposomal irinotecan + sintilimab + anlotinib is a combination therapy regimen being evaluated for the treatment of recurrent or persistent ovarian clear cell carcinoma (OCCC). The regimen consists of liposomal irinotecan, a nanoparticle-encapsulated topoisomerase I inhibitor that induces DNA damage in cancer cells; sintilimab, a humanized monoclonal antibody that targets the programmed cell death protein 1 (PD-1) receptor to restore anti-tumor immune responses; and anlotinib, an oral multi-target tyrosine kinase inhibitor that suppresses tumor angiogenesis and growth by inhibiting VEGFR, FGFR, PDGFR, and c-Kit. This triplet combination is currently being studied in a Phase II clinical trial (NCT06143371) sponsored by Sun Yat-Sen Memorial Hospital of Sun Yat-Sen University to assess its efficacy and safety in patients with OCCC, a subtype of ovarian cancer known for its poor prognosis and resistance to standard platinum-based chemotherapy.
- Brand names
- Fukanghua
- Other names
- Liposomal irinotecan, sintilimab, and anlotinib combinationIrinotecan liposome injection + sintilimab + anlotinib
02
Targets
TOP1 (DNA Topoisomerase I)KIT (c-KIT proto-oncogene receptor tyrosine kinase)PDCD1 (Programmed cell death protein 1 receptor)VEGFR-1 (Vascular endothelial growth factor receptor 1)VEGFR2 (Vascular endothelial growth factor receptor 2)VEGFR4 (Vascular endothelial growth factor Receptor-3)FGFR1 (Fibroblast growth factor receptor 1)FGFR2 (Keratinocyte growth factor receptor)FGFR3 (Fibroblast growth factor receptor 3)FGFR4 (Fibroblast growth factor receptor 4)PDGFRA (Platelet-derived growth factor receptor alpha)PDGFRB (Platelet-derived growth factor receptor beta)
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