Drug intelligence / Profile preview

IBI363 + fruquintinib

Development stage
Phase 1
Lead developer
Suzhou Innovent Biologics
Modality
Bispecific Antibodies → Multispecific Antibodies → Engineered Antibody Formats → Antibody-Based Therapeutics, Fc-Fusion Proteins → Carrier/Scaffold Proteins → Recombinant Proteins and Enzymes, Small Molecules
Administration
Intravenous, Oral
01

Overview

IBI363 + fruquintinib is a combination therapy currently being evaluated in Phase 1 clinical trials for the treatment of advanced colorectal cancer, specifically targeting patients with microsatellite stable (MSS) or proficient mismatch repair (pMMR) tumors. IBI363 is a first-in-class bispecific antibody fusion protein that simultaneously blocks the Programmed Cell Death Protein 1 (PD-1) pathway and provides biased Interleukin-2 (IL-2) signaling. By targeting IL-2α (CD25), IBI363 is designed to selectively stimulate tumor-specific T cells while minimizing the systemic toxicity typically associated with high-dose IL-2 therapy. Fruquintinib (also referred to as furuitinib) is a highly selective and potent small molecule tyrosine kinase inhibitor that targets Vascular Endothelial Growth Factor Receptors (VEGFR) 1, 2, and 3, thereby inhibiting tumor angiogenesis. The combination is intended to convert immunologically "cold" tumors into "hot" tumors by combining immune checkpoint blockade and cytokine stimulation with anti-angiogenic effects.

Other names
IBI363 + furuitinibIBI363 plus fruquintinibIBI-363 plus fruquintinibIBI 363 plus fruquintinibIBI363 plus furuitinibIBI-363 plus furuitinibIBI 363 plus furuitinib
02

Targets

FGFR1 (Fibroblast growth factor receptor 1)IL2RA (Interleukin-2 receptor alpha subunit)IL2RB (IL-2 receptor beta chain)IL2RG (Interleukin-2 receptor gamma subunit)PDCD1 (Programmed cell death protein 1 receptor)RET (Rearranged during transfection receptor tyrosine kinase)VEGFR-1 (Vascular endothelial growth factor receptor 1)VEGFR2 (Vascular endothelial growth factor receptor 2)VEGFR4 (Vascular endothelial growth factor Receptor-3)KIT (c-KIT proto-oncogene receptor tyrosine kinase)

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