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Study identifier: NCT06712004 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

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

Condition: Ischemic Stroke, Acute · Ischemic Stroke · Cerebral Infarction  ·  Sponsor: Zhujiang Hospital

PhasePhase 2
Planned participants40
Who can joinAll sexes, 18 Years to 80 Years
Healthy volunteersNo

About this study

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.

This description comes directly from the study's public registry record.

Talk to the study team

Chuanzhi Duan, MD  ·  02062782757  ·  doctor_duanzj@163.com

Xin Feng, MD  ·  13681134001  ·  13681134001@163.com

Always discuss trial participation with your own doctor first.

Locations (1)

Zhujiang Hospital of Southern Medical UniversityGuangzhou, Guangdong, ChinaRecruiting

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Source record: clinicaltrials.gov/study/NCT06712004