Drug intelligence / Profile preview

ilf2 antisense oligonucleotide

Development stage
Preclinical
Lead developer
Ionis Pharmaceuticals
Modality
Antisense Oligonucleotides (ASOs) → Long RNA Therapeutics → RNA Therapeutics → Nucleic Acid Therapeutics, Modified DNA Oligonucleotides → Antisense DNA → DNA Therapeutics → Nucleic Acid Therapeutics, Single-strand DNA → Antisense DNA → DNA Therapeutics → Nucleic Acid Therapeutics
Administration
Intravenous
01

Overview

ILF2 antisense oligonucleotide is a research-stage therapeutic developed by Ionis Pharmaceuticals in collaboration with the MD Anderson Cancer Center. It is designed to target and deplete Interleukin Enhancer Binding Factor 2 (ILF2), a protein that modulates the DNA repair pathway and is overexpressed in approximately 70% of relapsed/refractory multiple myeloma patients, particularly those with 1q21 chromosomal amplification. The oligonucleotide utilizes constrained ethyl (cEt) chemistry to improve RNA affinity, metabolic stability, and tissue half-life. By reducing ILF2 levels, the drug induces DNA damage, inhibits cell proliferation, and enhances the sensitivity of myeloma cells to DNA-damaging agents such as melphalan and bortezomib.

Other names
ILF2-targeting antisense oligonucleotideILF-2-targeting antisense oligonucleotideILF 2-targeting antisense oligonucleotide
02

Targets

RNASEH1 (Ribonuclease H1)ILF2 (Interleukin enhancer-binding factor 2)

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