Drug intelligence / Profile preview

liposomal ropivacaine hydrochloride

Development stage
Phase 1
Lead developer
Luye Pharma
Modality
Small Molecules, Lipid-based Nanoparticles → Nanoparticles → Drug Delivery Systems
Administration
Parenteral
01

Overview

Liposomal ropivacaine hydrochloride (LY09606) is a multivesicular liposome formulation of the long-acting amide local anesthetic ropivacaine hydrochloride. Developed by Luye Pharma, LY09606 is designed for local infiltration to provide sustained-release postoperative analgesia. Ropivacaine acts as a sodium channel blocker, preventing the generation and conduction of nerve impulses to produce local anesthesia and analgesia. The multivesicular liposome structure of LY09606 allows for a slow, controlled release of ropivacaine, extending the duration of action and potentially reducing the need for postoperative opioids or continuous infusion devices while minimizing systemic cardiac and central nervous system toxicities compared to bupivacaine-based liposomal formulations. It is currently in Phase I clinical development in China for postoperative pain management, such as after hemorrhoidectomy.

Other names
ropivacaine hydrochloride liposomeropivacaine hydrochloride liposome suspension injection
02

Targets

KCNQ1 (Potassium voltage-gated channel subfamily KQT member 1)SCN10A (Sodium channel protein type X alpha subunit)NaV alpha (Voltage-gated sodium channel alpha subunit family)

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