Clinical trials
Follow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
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.
Beyond the preview
Explore the evidence, development activity, and competitive landscape with Gosset’s full data platform.
Follow clinical development from study design and recruitment through results.
Explore development by indication, patient population, and geography.
Trace asset ownership, licensing agreements, and commercial partnerships.
Explore the patent landscape and regulatory exclusivity around an asset.
Compare development programs by target, modality, and indication.
Connect source evidence and development news to your research questions.
See how Gosset can support your research on chloroprocaine hydrochloride 2% injection.