Drug intelligence / Profile preview

conbercept + paclitaxel

Development stage
Unknown
Lead developer
Chengdu Kanghong Biotechnology
Modality
Small Molecules, Fc-Fusion Proteins → Carrier/Scaffold Proteins → Recombinant Proteins and Enzymes
Administration
Intravenous
01

Overview

KH903 (conbercept) in combination with paclitaxel is an investigational therapeutic regimen being developed by Chengdu Kanghong Biotech for the treatment of advanced gastric adenocarcinoma and gastroesophageal junction (GEJ) adenocarcinoma. Conbercept is a recombinant fusion protein biologic that functions as a VEGF trap; it is composed of the second immunoglobulin-like domain of VEGF receptor 1 (VEGFR1) and the third and fourth domains of VEGF receptor 2 (VEGFR2) fused to the Fc fragment of human IgG1. This decoy receptor binds with high affinity to VEGF-A, VEGF-B, and placental growth factor (PlGF), thereby inhibiting tumor angiogenesis and depriving the tumor of necessary blood supply and nutrients. Paclitaxel is a cytotoxic chemotherapy agent that stabilizes microtubules, leading to cell cycle arrest and apoptosis. The combination is currently being evaluated in Phase 2 clinical trials as a second-line treatment for patients who have progressed after initial platinum and fluoropyrimidine-based therapy.

Brand names
Lumitin
Other names
KH903 + paclitaxelconbercept + paclitaxel
02

Targets

VEGFB (Vascular endothelial growth factor B)TUBB (Tubulin (alpha and beta subunits))VEGFA (Vascular endothelial growth factor A)PGF (Placental Growth Factor)

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