drugset / Trial / NCT02954978

Impact of Nilotinib on Safety, Tolerability, Pharmacokinetics and Biomarkers in Parkinson's Disease

NCT02954978

Phase 2 Completed 75 enrolled Georgetown University
RandomizedParallel-groupQuadruple-blindTreatment

Summary

Parkinson's disease (PD) is the second most common neurodegenerative disorder causing motor and non-motor symptoms. PD is characterized by death of dopaminergic (DA) neurons in the substantia nigra (SN) pars compacta and formation of inclusions known as Lewy bodies (LBs) that primarily contain aggregated alpha-Synuclein. Nilotinib (Tasigna®, AMN107, Novartis, Switzerland) is approved by U.S. Food and Drug Administration (FDA) and is well tolerated for CML treatment at oral doses of 600-800mg daily. Nilotinib penetrates the brain and promotes autophagic degradation of alpha-Synuclein and p-Tau, leading to survival of DA neurons and improvement of motor function in PD models. For these studies, Nilotinib (1-10mg/kg daily) was used at significantly less than the clinically approved dose (up to 1200mg daily) in CML.

Timeline

Start
2017-01
Primary completion
2020-05
Completion
2020-07

Drugs

EvaluationDrugModalityDoseRoute
Comparator Nilotinib Small molecule 150 mg Oral
Comparator Nilotinib Small molecule 300 mg Oral

Indications