drugset / Trial / NCT02947893

Impact of Nilotinib on Safety, Biomarkers and Clinical Outcomes in Mild to Moderate Alzheimer's Disease

NCT02947893

Phase 2 Completed 37 enrolled Georgetown University
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The investigators hypothesize that Nilotinib will be safe in individuals with mild to moderate AD. Specifically, investigators hypothesize that low daily oral doses of Nilotinib will lead to CSF penetration, CNS Abl inhibition, and stabilization of CSF total Tau and p-Tau231/181 and Abeta42/40 levels. The investigators hypothesize that Nilotinib will decrease brain load of amyloid using amyloid positron emission tomography (PET). The investigators also predict that Nilotinib will reduce CSF markers of cell death, including neuron specific enolase (NSE) and S100B.

Timeline

Start
2017-01
Primary completion
2020-12
Completion
2021-03

Drugs

EvaluationDrugModalityDoseRoute
Comparator Nilotinib Small molecule 300 mg Oral

Indications