drugset / Trial / NCT04091945

A Study to Evaluate the Safety and Potential Efficacy of LT3001 Drug Product in Subjects With AIS

NCT04091945 ↗

Phase 2 Completed 24 enrolled Lumosa Therapeutics Co., Ltd.
RandomizedParallel-groupTriple-blindTreatment

Summary

This is a multicenter, double-blind, single-dose, randomized, and placebo-controlled prospective Phase IIa clinical study, designed to evaluate LT3001 drug product versus placebo/control in subjects with AIS.

Timeline

Start
2020-01-27
Primary completion
2021-02-22
Completion
2021-02-22

Drugs

EvaluationDrugModalityDoseRoute
Comparator Odatroltide Peptide 0.025 mg/kg Intravenous

Indications