drugset / Trial / NCT06712004
A Dose-Response Controlled Trial of Bevifibatide for Acute Ischemic Stroke
RandomizedParallel-groupDouble-blindTreatment
Summary
BCAIS-I is a single-center, randomized, double-blind, dose-response controlled clinical Trial, to preliminarily explore the efficacy of two different maintenance doses of bevifibatide citrate injection in improving 90-day neurological outcomes and the incidence of symptomatic intracranial hemorrhage in patients with acute ischemic stroke without large or medium-sized vessel occlusion, aiming to identify a dosing regimen that maintains therapeutic efficacy while minimizing the rates of symptomatic intracranial hemorrhage and serious adverse events, thereby providing dosing evidence for future large-scale randomized controlled trials.
Timeline
- Start
- 2025-02-10
- Primary completion
- 2025-09-01
- Completion
- 2025-12-01
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Bevifibatide | Unknown | 2 ug/kg | Intravenous |
| Subject | Bevifibatide | Unknown | 2.5 ug/kg | Intravenous |