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NCT04091945 · ClinicalTrials.gov registry record · Phase 2

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

A Phase 2 study of Acute Ischemic Stroke, sponsored by Lumosa Therapeutics Co..

Completed
Registry status
Phase 2
Development phase
24
Enrollment target
10
Study locations

NCT04091945 is a Phase 2 study of Acute Ischemic Stroke that has completed, run by Lumosa Therapeutics Co.. The registered enrollment target is 24 participants, below the 351-participant average among 25 other Acute Ischemic Stroke trials with a reported enrollment target (93% lower). The trial reports 10 study locations across 5 states.

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The verdict

NCT04091945, a Phase 2 study of Acute Ischemic Stroke, has completed, sponsored by Lumosa Therapeutics Co..

COMPLETED
Registry status
Phase 2
Development phase
24 participants
Enrollment target
10
Study locations

Study 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.

Conditions Studied

Interventions

  • DRUG Placebo
  • DRUG LT3001 Drug Product

Study Locations (10)

Other

  • Kaohsiung Medical University Chung-Ho Memorial Hospital - Kaohsiung City
  • Linkou Chang Gung Memorial Hospital - New Taipei City
  • Taipei Medical University - Shuang Ho Hospital - New Taipei City
  • China Medical University Hospital - Taichung
  • Taichung Veterans General Hospital - Taichung
  • Taipei Veterans General Hospital - Taipei

Kentucky

  • University of Kentucky Chandler Medical Center - Lexington

New Jersey

  • JFK Neuroscience Institute, JFK Medical Center - Edison

Ohio

  • The Ohio State University - Wexner Medical Center - Columbus

Tennessee

  • Chattanooga Center for Neurologic Research - Chattanooga

Trial Details

FieldValue
Enrollment Target 24 participants
Start Date 2020-01-27
Est. Completion 2021-02-22
Phase Phase 2

Sponsor

Lumosa Therapeutics Co.

5 total trials

What the Registry Record Tells You About NCT04091945

The ClinicalTrials.gov registry entry for NCT04091945 describes a study currently listed as completed, categorized as Phase 2. The registered enrollment target is 24 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 351-participant average among 25 other Acute Ischemic Stroke trials with a reported enrollment target (93% lower). The listed sponsor is Lumosa Therapeutics Co., which has 5 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Acute Ischemic Stroke appearing as the primary indexed condition, and to 2 interventions - of which Placebo is the first listed.

NCT04091945 reports 10 study locations spanning 5 distinct geographic areas - top geographies include Other, Kentucky, New Jersey.

Frequently Asked Questions

What is clinical trial NCT04091945 about?

NCT04091945 is a clinical study titled "A Study to Evaluate the Safety and Potential Efficacy of LT3001 Drug Product in Subjects With AIS". 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.

What is the current status of trial NCT04091945?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 24 participants. The study started on 2020-01-27. Estimated completion is 2021-02-22.

What conditions does trial NCT04091945 study?

This clinical trial studies the following conditions: Acute Ischemic Stroke.

What interventions are being tested in trial NCT04091945?

The interventions under investigation include: Placebo (DRUG), LT3001 Drug Product (DRUG).

Who is sponsoring clinical trial NCT04091945?

This trial is sponsored by Lumosa Therapeutics Co., which has 5 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT04091945 being conducted?

This trial has 10 study locations across Kentucky, New Jersey, Ohio, Tennessee. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

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