Drug intelligence / Profile preview

clevidipine

Development stage
Approved
Lead developer
Novartis
Modality
Small Molecules
Administration
Intravenous
01

Overview

Clevidipine is a third-generation, intravenous, dihydropyridine L-type calcium channel blocker used for the rapid reduction of blood pressure when oral antihypertensive therapy is not feasible or desirable. It acts by selectively inhibiting calcium influx in vascular smooth muscle cells, leading to arterial vasodilation and decreased systemic vascular resistance without significant effects on cardiac contractility or conduction. Clevidipine has a very short half-life (~1 minute), allowing for precise titration and rapid onset/offset of action. It is indicated primarily for acute hypertension management in perioperative settings and emergencies where oral administration is not possible. The drug is formulated as a lipid emulsion and metabolized rapidly by esterases in blood and tissues, making its clearance independent of renal or hepatic function[2][3][4][5][6].

Brand names
Cleviprex
Other names
clevidipine butyrate
02

Targets

CACNA1C (Voltage-dependent L-type calcium channel subunit alpha-1C)

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