drugset / Trial / NCT07617870
Pro-urokinase for Extended-Window Posterior Circulation Stroke
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Comparator | Asprin (300mg) | Unknown | 300 mg | Oral |
| Subject | rhPro-UK | Protein / enzyme biologic | 35 mg | Intravenous |