drugset / Trial / NCT07581210

Efficacy and Safety of QD202 in Participants With Acute Ischemic Stroke Undergoing Thrombolysis Excluding Endovascular Thrombectomy

NCT07581210 ↗

Phase 2 Recruiting 120 enrolled Shanghai QuietD Biotechnology Co., Ltd.
RandomizedParallel-groupTriple-blindTreatment

Summary

This is a randomized, double-blinded, placebo-controlled study investigating the safety and efficacy of QD202 injection in patients with acute ischemic stroke undergoing thrombolysis excluding endovascular thrombectomy. Up to 120 male and female patients with acute ischemic stroke undergoing thrombolysis excluding endovascular thrombectomy will be dosed with QD202 injection or placebo as a 60 minute intravenous infusion after completion of the thrombolysis procedure on Day 1-5 of the study period. Subjects will undergo interim procedures at Day 7 or the day of discharge, Day 30, and end-of-study procedures on Day 90.

Timeline

Start
2025-10-14
Primary completion
2026-08
Completion
2026-12

Drugs

EvaluationDrugModalityDoseRoute
Subject QD202 Peptide 5 mg Intravenous
Subject QD202 Peptide 10 mg Intravenous

Indications