A 52-Week, Multicenter, Phase 1 Open-label Study to Evaluate the Safety of LX1001 in Participants With APOE4 Homozygote Alzheimer's Disease
Latest Information Update: 26 Nov 2024
At a glance
- Drugs LX 1001 (Primary)
- Indications Alzheimer's disease; Mild cognitive impairment
- Focus Adverse reactions
- Sponsors LEXEO Therapeutics
Most Recent Events
- 22 Nov 2024 Status changed from active, no longer recruiting to completed.
- 30 Oct 2024 According to a Lexeo Therapeutics media release, Company has initiated engagement with FDA on these data and expects to provide an update on regulatory interactions and further LX1001 development plans in 2025.
- 30 Oct 2024 According to a Lexeo Therapeutics media release, Dr. Kim Johnson is the principal investigator of the trial.