drugset / Trial / NCT06421532

Stimulating Amyloid Clearance in Cerebral Amyloid Angiopathy

NCT06421532 ↗

Phase 2 Enrolling by invitation 60 enrolled Leiden University Medical Center The Dutch Brain Foundation · collab
RandomizedParallel-groupOpen-labelTreatment

Summary

A pre-post study will be conducted to assess whether treatment with LXB, nVNS or a combination of both interventions can enhance the clearance of Aβ in patients with CAA. A total of 60 subjects, 30 with sCAA and 30 with D-CAA, will be randomly assigned to receive LXB, or both interventions. The primary outcome measure will be the morning levels of Aβ40 and Aβ42 in cerebrospinal fluid (CSF) before and after the intervention. The investigators will assess disease progression with (non-)haemorrhagic imaging markers on 7-Tesla Magnetic Resonance Imaging (7-T MRI) as a secondary outcome. Additionally, the activity of the glymphatic system by means of fluid dynamics will be assessed using 7-T MRI.

Timeline

Start
2025-03-27
Primary completion
2027-09-27
Completion
2027-09-27

Drugs

EvaluationDrugModalityDoseRoute
Subject XYWAV Unknown — —