Drug intelligence / Profile preview

JX-594 + irinotecan

Development stage
Unknown
Lead developer
SillaJen
Modality
Nucleic Acid-Directed Small Molecules → Small Molecules, Oncolytic Viruses → Oncolytic Therapeutics, Covalent Small Molecules → Small Molecules, Classical Binding Small Molecules → Small Molecules
Administration
Intravenous
01

Overview

JX-594 + irinotecan is an investigational combination therapy for cancer that pairs two distinct agents: - **JX-594 (Pexa-Vec, pexastimogene devacirepvec)** is a genetically engineered oncolytic vaccinia virus designed to selectively infect and lyse cancer cells. It has been modified to express human granulocyte-macrophage colony-stimulating factor (GM-CSF) and β-galactosidase, enhancing tumor-specific immune responses. The virus preferentially replicates in tumor cells due to their high thymidine kinase activity and defects in interferon signaling pathways. Its mechanisms include direct oncolysis of tumor cells, induction of anti-tumor immunity via GM-CSF expression, and disruption of tumor vasculature[6][8][9]. - **Irinotecan** is a small molecule chemotherapeutic agent that inhibits topoisomerase I, leading to DNA damage and apoptosis in rapidly dividing cells. The combination has been studied primarily in patients with metastatic colorectal cancer who are refractory or intolerant to standard therapies. Early-phase clinical trials have evaluated the safety, tolerability, and preliminary efficacy of this regimen[1][3][4].

Brand names
Pexa-Vec
Other names
JX-594 + irinotecan combination
02

Targets

TOP1 (DNA Topoisomerase I)

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