drugset / Trial / NCT07617870

Pro-urokinase for Extended-Window Posterior Circulation Stroke

NCT07617870

Phase 3 Not yet recruiting 586 enrolled The First Affiliated Hospital of Zhengzhou University
RandomizedParallel-groupQuadruple-blindTreatment

Summary

This study aims to evaluate whether, in patients with imaging-confirmed acute ischemic stroke of the posterior circulation presenting within 4.5-24 hours after symptom onset and not scheduled for endovascular thrombectomy, intravenous thrombolysis with recombinant human prourokinase (rhPro-UK), compared with standard medical treatment, can achieve superior 90-day functional outcomes with a higher level of safety.

Timeline

Start
2026-06-01
Primary completion
2027-12-31
Completion
2028-06-30

Drugs

EvaluationDrugModalityDoseRoute
Comparator Asprin (300mg) Unknown 300 mg Oral
Subject rhPro-UK Protein / enzyme biologic 35 mg Intravenous

Indications