a Study Evaluating the Safety and Efficacy of Clevidipine for Patients Who With Hypertensive Emergency and Sub-emergency

Hypertensive Emergency Clinical Trial

Official title:
A Multicentre, Randomized, Double-blind, Parallel Design Phase III Study to Evaluate the Efficacy and Safety of Intravenous QLG2071 Versus Cleviprex® for Patients With Hypertensive Emergency and Sub-emergency

Status Not yet recruiting

Clinical Trial Summary

A Multicentre, Randomized, Double-blind, Parallel Design Phase III Study to Evaluate the efficacy and safety of QLG2071 Versus Cleviprex® in the Treatment of Hypertensive Emergency and Sub-emergency

Clinical Trial Description

This is a multicenter, randomized, double-blind, active-compared Phase III clinical study to evaluate the efficacy and safety of clevidipine butyrate injectable emulsion in the treatment of Hypertensive Emergency and Sub-emergency. The Cleviprex® will be chosen as the positive controlled medicine with the same usage of the test drug ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT05922436
Study type	Interventional
Source	Qilu Pharmaceutical (Hainan) Co., Ltd.
Contact	Yuguo Chen
Phone	0531-82169022
Email	chen919085@126.com
Status	Not yet recruiting
Phase	Phase 3
Start date	July 15, 2023
Completion date	May 25, 2024

View Details

See also
Status	Clinical Trial	Phase
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Active, not recruiting	`NCT05155202` - Clinical Relevance of Nicardipine Induced Hypoxemia in the Intensive Care Unit
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