Y-3 for Injection in the Treatment of Acute Ischemic Stroke

PHASE3RecruitingINTERVENTIONAL
Enrollment

998

Participants

Timeline

Start Date

July 24, 2024

Primary Completion Date

December 31, 2024

Study Completion Date

July 31, 2025

Conditions
Acute Ischemic Stroke
Interventions
DRUG

Y-3 for injection

Qualified subjects were randomly divided into groups in a 1:1 ratio and received continuous treatment with Y-3 injection (40 mg/dose, qd) or placebo control drug. The treatment was performed 10 times for 10 days.

DRUG

Placebo control group

Qualified subjects were randomly divided into groups in a 1:1 ratio and received continuous treatment with Y-3 injection (40 mg/dose, qd) or placebo control drug. The treatment was performed 10 times for 10 days.

Trial Locations (1)

100000

RECRUITING

Beijing Tiantan Hospital Capital Medical University Beijing, Beijing

Sponsors
All Listed Sponsors
collaborator

Neurodawn Pharmaceutical Co., Ltd.

INDUSTRY

lead

Beijing Tiantan Hospital

OTHER