Drug intelligence / Profile preview

LiCO-saUcp1

Development stage
Preclinical
Lead developer
Ractigen Therapeutics
Modality
Small RNA Therapeutics → RNA Therapeutics → Nucleic Acid Therapeutics
Administration
Subcutaneous
01

Overview

LiCO-saUcp1 is a first-in-class, adipose-biased, lipid-conjugated small activating RNA (saRNA) designed to treat obesity and metabolic disorders. Developed by Ractigen Therapeutics, it utilizes RNA activation (RNAa) technology to specifically target the promoter of the Uncoupling protein 1 (UCP1) gene, inducing its expression and promoting the browning of white adipose tissue. In preclinical studies using diet-induced obesity (DIO) mice, subcutaneous administration of LiCO-saUcp1 resulted in significant, durable weight loss characterized by selective fat mass reduction and preservation of lean mass. It also demonstrated potential in treating hepatic steatosis by lowering liver triglycerides and showed synergistic efficacy when combined with GLP-1 receptor agonists like semaglutide.

02

Targets

UCP1 (Uncoupling protein 1)

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