CI

At a glance

ClinicalIndex Comparison Record
Phase 2Completed· 89 enrolled
Drug / intervention
LT3001 Drug Product +1 moredrug
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT05403866
NCT05403866Phase 2Completed

A Phase II, Double-Blind, Randomized, Placebo-Controlled Study to Evaluate the Safety and Efficacy of Multiple Doses of LT3001 Drug Product in Subjects With Acute Ischemic Stroke (AIS)

Lumosa Therapeutics Co., Ltd.·interventional·Posted Jun 3, 2022·Updated Dec 26, 2025

In Brief

A Phase 2 clinical trial evaluating LT3001 Drug Product and Placebo for Acute Ischemic Stroke. Completed, enrolled 89 participants across 1 site.

Detailed Summary

This is a phase II, double-blind, randomized, placebo-controlled study to evaluate the safety and efficacy of multiple doses of LT3001 drug product in subjects with acute ischemic stroke (AIS)

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesUnited States
Collaborators--

Timeline

Phase 2CompletedFinished
2023202420252026
First PostedJun 3, 2022
Enrollment StartAug 17, 2022
Primary CompletionMay 23, 2025
TodayJul 2, 2026
Enrollment to primary: 2.8 yearsPosted 4.1 years ago

Interventions

LT3001 Drug Productdrug

Administered by intravenous infusion

Placebodrug

Administered by intravenous infusion