A Phase II, Two-Part, Double-Blind, Randomized, Placebo Controlled Study to Evaluate the Safety and Efficacy of LT3001 Drug Product in Subjects With Acute Ischemic Stroke (AIS) Undergoing Endovascular Thrombectomy (EVT)
Latest Information Update: 11 Jun 2025
At a glance
- Drugs LT 3001 (Primary)
- Indications Stroke
- Focus Therapeutic Use
- Sponsors Lumosa Therapeutics
Most Recent Events
- 05 Jun 2025 Planned End Date changed from 30 Apr 2024 to 31 Mar 2026.
- 05 Jun 2025 Planned primary completion date changed from 30 Apr 2024 to 31 Mar 2026.
- 02 Feb 2024 Status changed from not yet recruiting to recruiting, according to Lumosa Therapeutics media release.