drugset / Trial / NCT03578822

Thrombolysis With rhPro-UK in 4.5-6 Hours After Acute Ischemic Stroke in a Double-blinded,Controlled Trial

NCT03578822

Phase 3 Completed 149 enrolled Tasly Biopharmaceuticals Co., Ltd.
RandomizedParallel-groupQuadruple-blindTreatment

Summary

This is a randomized,controlled, double-blinded, phase 3 clinical study to evaluate the efficacy and safety of recombinant human urokinase(rhPro-UK) versus basic treatment for patients with acute ischaemic stroke in 4.5-6 hours after stroke onset.

Timeline

Start
2018-08-10
Primary completion
2020-02-28
Completion
2020-03-01

Drugs

EvaluationDrugModalityDoseRoute
Subject Aspirin Small molecule 300 mg Oral
Subject rhPro-UK Protein / enzyme biologic 35 mg Other

Indications