drugset / Trial / NCT05400330

Long-Term Follow-up of Gene Therapy for APOE4 Homozygote Alzheimer's Disease

NCT05400330 ↗

Phase 1 Active not recruiting 10 enrolled Lexeo Therapeutics
NaSingle-groupOpen-labelTreatment

Summary

The primary purpose of this long-term follow-up study is to assess the long-term safety profile of APOE4 homozygote participants who were administered gene therapy (LX1001) for the treatment of Alzheimer's disease in Study LX100101. A secondary objective is to assess the biomarker as shown by the conversion of CSF APOE isoforms from APOE4 to APOE2-APOE4. Additional secondary outcomes include amyloid PET scan, CSF markers (including Aβ42, Aβ42/Aβ40 ratio T--tau, and P-tau), and quantitative MRI (and other biomarkers that may be informative for this therapeutic approach). Other secondary objectives include instruments to assess cognitive and clinical AD and to evaluate if treatment with AAVrh.10hAPOE2 improves brain tau pathology with tau PET scan (LX1001-01 Cohorts 3 and 4 only).

Timeline

Start
2023-05-08
Primary completion
2028-11
Completion
2028-11

Drugs

EvaluationDrugModalityDoseRoute
Subject LX1001 Gene therapy (AAV / viral vector) 1.4e+10 unknown —
Subject LX1001 Gene therapy (AAV / viral vector) 4.4e+10 unknown —
Subject LX1001 Gene therapy (AAV / viral vector) 1.4e+11 unknown —
Subject LX1001 Gene therapy (AAV / viral vector) 1.4e+14 unknown —

Indications