The Androtriol Injection for the Treatment of Acute Ischemic Stroke

PHASE2Not yet recruitingINTERVENTIONAL
Enrollment

300

Participants

Timeline

Start Date

October 31, 2024

Primary Completion Date

September 30, 2025

Study Completion Date

October 30, 2025

Conditions
Acute Ischemic Stroke
Interventions
DRUG

Androtriol Injection (High-dose group)

Participants will receive 30 mL of Androtriol Injection per dose, administered every 12 hours for 7 consecutive days. Each infusion will be administered over a period of 30±5 minutes.

DRUG

Androtriol Injection (Low-dose group)

Participants will receive 10 mL of Androtriol Injection combined with 20 mL of placebo (Hydroxypropyl Beta-Cyclodextrin Injection) per dose, administered every 12 hours for 7 consecutive days. Each infusion will be administered over a period of 30±5 minutes.

DRUG

Hydroxypropyl-β-cyclodextrin injection

Participants will receive 30 mL of Hydroxypropyl-β-cyclodextrin injection per dose, administered every 12 hours for 7 consecutive days. Each infusion will be completed within 30±5 minutes.

All Listed Sponsors
lead

Beijing Tiantan Hospital

OTHER

NCT06679322 - The Androtriol Injection for the Treatment of Acute Ischemic Stroke | Biotech Hunter | Biotech Hunter