drugset / Trial / NCT05922436

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

NCT05922436

Phase 3 Unknown 378 enrolled Qilu Pharmaceutical (Hainan) Co., Ltd.
RandomizedParallel-groupTriple-blindTreatment

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

Timeline

Start
2023-07-15
Primary completion
2024-05-24
Completion
2024-05-25

Drugs

EvaluationDrugModalityDoseRoute
Subject Clevidipine Small molecule 25 mg Intravenous

Indications