Drug intelligence / Profile preview

IMO-3100

Development stage
Phase 2
Lead developer
Aceragen
Modality
Small Molecules, MicroRNA (miRNA) → Small RNA Therapeutics → RNA Therapeutics → Nucleic Acid Therapeutics, 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, Small Interfering RNA (siRNA) → Small RNA Therapeutics → RNA Therapeutics → Nucleic Acid Therapeutics
Administration
Subcutaneous
01

Overview

IMO-3100 is a synthetic DNA-based antagonist of Toll-like receptor 7 (TLR7) and Toll-like receptor 9 (TLR9), developed for the treatment of autoimmune and inflammatory diseases. It acts by inhibiting TLR7- and TLR9-mediated immune responses, thereby reducing the production of multiple pro-inflammatory cytokines such as IL-6, TNF-alpha, IFN-gamma, IP-10, and others. Unlike therapies that target individual cytokines, IMO-3100 blocks upstream signaling pathways involved in inflammation. Preclinical studies have demonstrated its efficacy in models of lupus, rheumatoid arthritis, psoriasis, hyperlipidemia, and other immune-mediated conditions. The drug was originally developed by Idera Pharmaceuticals (now Aceragen) and has reached Phase 2 clinical development for indications including plaque psoriasis[1][2][3][4][5][6].

02

Targets

TLR9 (Toll-like receptor 9)TLR7 (Toll-like receptor 7)

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