Drug intelligence / Profile preview

iparomlimab + regorafenib

Development stage
Unknown
Lead developer
Qilu Pharmaceutical
Modality
Monoclonal Antibodies → Antibody-Based Therapeutics, Small Molecules
Administration
Intravenous, Oral
01

Overview

Iparomlimab + regorafenib is an investigational combination therapy consisting of iparomlimab, a humanized IgG4 monoclonal antibody targeting the programmed cell death protein 1 (PD-1) receptor, and regorafenib, an oral multi-kinase inhibitor. Iparomlimab functions as a checkpoint inhibitor, blocking the interaction between PD-1 and its ligands (PD-L1 and PD-L2) to reactivate T-cell mediated anti-tumor immunity. Regorafenib inhibits a broad range of protein kinases involved in tumor angiogenesis (VEGFR1-3, TIE2), oncogenesis (KIT, RET, RAF-1, BRAF), and the tumor microenvironment (PDGFR, FGFR). This combination is being explored for its potential synergistic effects, where regorafenib-mediated modulation of the tumor microenvironment and angiogenesis may enhance the efficacy of PD-1 blockade. Clinical development is notably being led by Peking Union Medical College Hospital for the treatment of advanced solid tumors, including anal squamous cell carcinoma, peritoneal mesothelioma, and peritoneal metastatic cancer.

Other names
QL1604 + regorafenib
02

Targets

RAF1 (c-Raf-1 (Y340D/Y341D))BRAF (B-Raf proto-oncogene, serine/threonine kinase)KIT (c-KIT proto-oncogene receptor tyrosine kinase)PDCD1 (Programmed cell death protein 1 receptor)TEK (Tie2)PDGFRB (Platelet-derived growth factor receptor beta)VEGFR3 (Vascular endothelial growth factor receptor 3)VEGFR-1 (Vascular endothelial growth factor receptor 1)VEGFR2 (Vascular endothelial growth factor receptor 2)FGFR1 (Fibroblast growth factor receptor 1)RET (Rearranged during transfection receptor tyrosine kinase)

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