Drug intelligence / Profile preview

OLX702A

Development stage
Unknown
Lead developer
Olix Pharmaceuticals
Modality
Chemically Modified siRNA → Small Interfering RNA (siRNA) → Small RNA Therapeutics → RNA Therapeutics → Nucleic Acid Therapeutics, MicroRNA (miRNA) → Small RNA Therapeutics → RNA Therapeutics → Nucleic Acid Therapeutics, Antisense Oligonucleotides (ASOs) → Long RNA Therapeutics → RNA Therapeutics → Nucleic Acid Therapeutics, Conjugated siRNA → Small Interfering RNA (siRNA) → Small RNA Therapeutics → RNA Therapeutics → Nucleic Acid Therapeutics, Antisense DNA → DNA Therapeutics → Nucleic Acid Therapeutics
Administration
Subcutaneous
01

Overview

**OLX702A** is a GalNAc-conjugated asymmetric small interfering RNA targeting **mitochondrial amidoxime reducing component 1** to silence hepatic **MTARC1** expression. It was originated by **OliX Pharmaceuticals** and is being developed for **metabolic-associated steatohepatitis** with additional preclinical rationale in **obesity**, including reported synergy with GLP-1 agonists such as semaglutide. The drug is formulated as a **subcutaneous injection** intended for infrequent dosing, including once-every-3-months administration, and entered **Phase 1** clinical testing in Australia. In 2025, **Eli Lilly** licensed rights to further develop and commercialize the program.

02

Targets

MTARC1 (Mitochondrial amidoxime-reducing component 1)

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