Drug intelligence / Profile preview

RP910

Development stage
Unknown
Lead developer
Runjia
Modality
Chemically Modified siRNA → Small Interfering RNA (siRNA) → Small RNA Therapeutics → RNA Therapeutics → Nucleic Acid Therapeutics, Conjugated siRNA → Small Interfering RNA (siRNA) → Small RNA Therapeutics → RNA Therapeutics → Nucleic Acid Therapeutics
Administration
Subcutaneous
01

Overview

RP910 is a small interfering RNA (siRNA) therapeutic designed to target and inhibit the production of **proprotein convertase subtilisin/kexin type 9 (PCSK9)**. Developed through a collaboration between **Risen Shanghai Medical Technology** (also known as Risen Suzhou Pharma Technology) and **TopAlliance**, the drug utilizes a proprietary **GalNAc (N-acetylgalactosamine)** delivery system to facilitate specific uptake by hepatocytes. By silencing the PCSK9 gene, RP910 reduces the circulating levels of the PCSK9 protein, which normally promotes the degradation of LDL receptors. This reduction leads to an increase in LDL receptor density on the surface of liver cells, thereby enhancing the clearance of LDL cholesterol from the blood. RP910 is primarily indicated for the treatment of **dyslipidemia** and the prevention of associated **cardiovascular diseases**.

02

Targets

PCSK9 (Proprotein convertase subtilisin/kexin type 9)

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