Drug intelligence / Profile preview

chloroprocaine hydrochloride 2% injection

Development stage
Unknown
Lead developer
Johns Hopkins University
Modality
Small Molecules
Administration
Epidural, Intraperitoneal, Percutaneous, Subcutaneous
01

Overview

Chloroprocaine hydrochloride 2% injection (brand name: Nesacaine) is a short-acting, amino-ester class local anesthetic. It exerts its anesthetic effect by binding to and blocking voltage-gated sodium channels in peripheral neurons, thereby preventing the influx of sodium ions required for the initiation and conduction of nerve impulses. Characterized by a rapid onset of action (6–12 minutes) and a short duration of action (up to 60 minutes), chloroprocaine is rapidly metabolized by plasma esterases, which minimizes the risk of systemic accumulation and toxicity. While FDA-approved for infiltration, nerve block, epidural, and caudal anesthesia, it is also being evaluated in Phase 3 clinical trials by Johns Hopkins University as an investigational intraperitoneal lavage agent to reduce postoperative pain and nausea in women undergoing elective cesarean delivery.

Brand names
NesacaineNesacaine-MPF
Other names
Chloroprocaine Hcl 2% Injchloroprocainechloroprocaine HClchloroprocaine HCl 2%chloroprocaine hydrochloridechloroprocaine hydrochloride 2%
02

Targets

NaV alpha (Voltage-gated sodium channel alpha subunit family)

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