drugset / Trial / NCT06679322

The Androtriol Injection for the Treatment of Acute Ischemic Stroke

NCT06679322 ↗

Phase 2 Not yet recruiting 300 enrolled Beijing Tiantan Hospital
RandomizedParallel-groupQuadruple-blindTreatment

Summary

This is a prospective, multicenter, randomized, double-blind, placebo-controlled, phase IIb clinical trial of Androtriol injection for the treatment of acute ischemic stroke. The goal of this trial is to explore the efficacy and safety of different doses of Androtriol injection in patients with acute ischemic stroke (AIS) who received vascular recanalization treatment within 24 hours of symptom onset. Participants will receive a low-dose Androtriol injection (100 mg BID), a high-dose Androtriol injection (300 mg BID), or a placebo intravenously within 24 hours of stroke onset. They will be treated twice daily (every 12 hours) for 7 days, with a total of 14 doses over the course of the study. Each infusion will last approximately 30±5 minutes.

Timeline

Start
2024-10-31
Primary completion
2025-09-30
Completion
2025-10-30

Drugs

EvaluationDrugModalityDoseRoute
Subject Androtriol Unknown 100 mg Intravenous
Subject Androtriol Unknown 300 mg Intravenous

Indications