drugset / Trial / NCT06712004

A Dose-Response Controlled Trial of Bevifibatide for Acute Ischemic Stroke

NCT06712004 ↗

Phase 2 Recruiting 40 enrolled Zhujiang Hospital
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

EvaluationDrugModalityDoseRoute
Subject Bevifibatide Unknown 2 ug/kg Intravenous
Subject Bevifibatide Unknown 2.5 ug/kg Intravenous

Indications