A Study to Evaluate the Safety and Efficacy of LT3001 Drug Product in Subjects AIS Undergoing EVT

PHASE2RecruitingINTERVENTIONAL
Enrollment

66

Participants

Timeline

Start Date

August 11, 2022

Primary Completion Date

March 31, 2026

Study Completion Date

March 31, 2026

Conditions
Acute Ischemic Stroke
Interventions
DRUG

LT3001 Drug Product

LT3001 Drug Product administered once by intravenous infusion

DRUG

Placebo

Placebo administered once by intravenous infusion

Trial Locations (2)

37404

RECRUITING

CHI Memorial Hospital, Chattanooga

Unknown

RECRUITING

Taichung Medical University, Taichung

Sponsors
All Listed Sponsors
lead

Lumosa Therapeutics Co., Ltd.

INDUSTRY