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NCT Number: NCT02281474

Nilotinib in Cognitively Impaired Parkinson Disease Patients 001

This pilot study will test Nilotinib's ability to alter the abnormal protein build up in Parkinson disease and Diffuse Lewey Body Disease patients . Patients will receive Nilotinib at different doses for 6 months. Patients will then be tested to see if there is change in three areas: 1) has the disease symptoms changed. 2) has levels of a specific misfolded protein changed in the fluid around their brain and spine. 3) Have inflammatory markers changed in the patient's blood and fluid around their brain and spine. If successful, this drug could be used to slow down or stop the progression of disorders that involve abnormal collection of misfolded proteins. However, the main purpose of this pilot study is to check for the safety of using this medication at this level.

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Key information

Conditions

Parkinson's Disease Basal Ganglia Diseases Brain Diseases Central Nervous System Diseases Dementia Diffuse Lewy Body Disease Lewy Body Disease Mental Disorders Movement Disorders Nervous System Diseases Neurocognitive Disorders Neurodegenerative Diseases Parkinson Disease Parkinson's Disease Dementia Parkinsonian Disorders Synucleinopathies

Age range

40 year–90 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 1

Primary location

MedStar Georgetown University Hospital

Washington D.C., District of Columbia, 20007, United States

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Patients aged 40 to 90 with Idiopathic Parkinson's Disease (Significant Sinemet response) on a stable medication drug regimen L-dopa and/or Dopamine agonist (at least 1 month before enrollment with no new medication change) and with moderate to severe cognitive impairment (MOCA ≤24).

Inclusions criteria:

  • Written informed consent
  • Capability and willingness to comply with the study related criteria
  • Patients between the age of 40-90 y
  • Diagnosis of PD according to the UK Brain Bank Diagnostic Criteria
  • Early PD subjects with MMSE between 23-30.
  • Hoehn and Yahr stage <2
  • Stable treatment (>4 weeks) with MAO-B inhibitor (Selegeline up to 10mg/d or rasagiline up to 1 mg/d) allowable
  • Patients not needing dopamine agonist or levodopa therapy presently or at least for the next 6 months
  • Idiopathic PD with NO genetic mutations (autosomal recessive or dominant)
  • Detectable levels of CSF for blood and CSF Alpha-Synuclein

Exclusion criteria

  • Patients with a known genetic form of PD that does not involve alpha-synuclein.
  • Unwillingness to undergo lumbar punctures
  • Immeasurable CSF α-synuclein.
  • Presence of dementia or severe cognitive impairment that would not permit the patient to give adequate feedback for potential side effects.
  • Unwilling to be in an off state for UPDRS assessment.
  • Pre-menopausal women
  • Patients with autosomal recessive (PARKIN, PINK1 or DJ1) or dominant mutations (LRRK2)
  • Patients with hypokalemia, hypomagnesaemia, or long QT syndrome.
  • Concomitant drugs known to prolong the QT interval
  • Strong CYP3A4 inhibitors
  • Any drugs or foods that may interact with Nilotinib as stated in the Package Insert (PI).
  • Medical history of liver and pancreatic diseases.
  • Clinical signs indicating syndromes other than idiopathic PD, including supranucelar gaze palsy, signs of frontal dementia, history of stroke, head injury or encephalitis, cerebellar sings, early severe autonomic involvement, Babinski's signs.
  • History of any cardiovascular disease, including hypertension, myocardial infraction or cardiac failure, angina, arrhythmia.

Treatment and study plan

Nilotinib

Drug

Other names: Tasigna

Primary outcomes

  1. Change in α-synuclein and Tau concentrations in the CSF and serum of patients

    Time frame: 6 months

    Working Hypothesis: PD patients have been shown to have elevated levels of α-synuclein in their CSF. Nilotinib has been shown to reduce α-synuclein and Tau in the gastrointestinal tract and central nervous system in animal models, and similarly, we propose will show changes in CSF and serum α-synuclein concentrations in nilotinib treated PD patients.

Secondary outcomes

  1. Determine nilotinib's efficacy by improvement in motor and non-motor symptoms

    Time frame: 6 months

    Working Hypothesis: By following strict safety guidelines, monitoring patients through physical examinations, self-examinations, laboratory and neurological examinations, nilotinib will be a safe drug to use in patients with PD and PD related patients.

    Determine if any clinical benefit is observed in this small, short, limited clinical trial.

    Working Hypothesis: In cell culture and animal models of PD, dopaminergic neurons have shown increased cell death with accumulating α-synuclein. Therefore, PD patients treated with nilotinib, which lowers α-synuclein and Tau in vivo and in vitro studies, will have improvement or stabilization of their motor UPDRS and cognition.

  2. Safety and tolerability, as measured by number of Participants with Adverse Events

    Time frame: 6 months

    Working Hypothesis: By following strict safety guidelines, monitoring patients through physical examinations, self-examinations, laboratory and neurological examinations, nilotinib will be a safe drug to use in patients with PD and PD related patients.

    Determine if any clinical benefit is observed in this small, short, limited clinical trial.

    Working Hypothesis: In cell culture and animal models of PD, dopaminergic neurons have shown increased cell death with accumulating α-synuclein. Therefore, PD patients treated with nilotinib, which lowers α-synuclein and Tau in vivo and in vitro studies, will have improvement or stabilization of their motor UPDRS and cognition.

Sponsors and collaborators

Lead sponsor

Georgetown University

Other

Registry information

Official study title

Open Label Dose Escalation of Nilotinib in Cognitively Impaired Parkinson Disease Patients With Elevated Cerebrospinal Fluid and Blood α-Synuclein

Important dates

Study start
2014
Primary completion
2015
First posted
Nov 3, 2014
Registry last updated
Dec 16, 2015

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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