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The Parkinson's Progression Markers Initiative (PPMI)

Conditions
Parkinson Disease
MedDRA version: 14.1Level: PTClassification code 10061536Term: Parkinson's diseaseSystem Organ Class: 10029205 - Nervous system disorders
Therapeutic area: Analytical, Diagnostic and Therapeutic Techniques and Equipment [E] - Diagnosis [E01]
Registration Number
EUCTR2010-019894-13-IT
Lead Sponsor
MICHAEL J. FOX FOUNDATION FOR PARKINSON'S RESEARCH
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Authorised-recruitment may be ongoing or finished
Sex
All
Target Recruitment
600
Inclusion Criteria

Parkinson Disease(PD)Subjects: 1.Patients must have at least two of the following: resting tremor, bradykinesia, rigidity (must have either resting tremor or bradykinesia); OR either asymmetric resting tremor or asymmetric bradykinesia. 2.A diagnosis of Parkinson disease for two years or less at Screening. 3.Hoehn and Yahr stage I or II. 4.Confirmation from imaging core that screening DAT scan is consistent with dopamine transporter deficit. 5.Not expected to require PD medication with at least 6 months from Baseline. 6.Male or female age 30 years or older at time of PD diagnosis. Healthy Control (HC)Subjects: 1.Male or female age 30 years or older at Screening. 2.Confirmation from imaging core that screening DAT scan is consistent with no dopamine transporter deficit.
Are the trial subjects under 18? no
Number of subjects for this age range: 0
F.1.2 Adults (18-64 years) yes
F.1.2.1 Number of subjects for this age range 300
F.1.3 Elderly (>=65 years) yes
F.1.3.1 Number of subjects for this age range 300

Exclusion Criteria

Parkinson Disease (PD) Subjects: 1.Currently taking levodopa, dopamine agonists, MAO-B inhibitors, amantadine or other PD medication. 2.Has taken levodopa, dopamine agonists, MAO-B inhibitors or amantadine within 60 days of Baseline. 3.Has taken levodopa or dopamine agonists prior to Baseline for more than a total of 60 days. 4.Received any of the following drugs that might interfere with DAT imaging: Neuroleptics, metoclopramide, alpha methyldopa, methylphenidate, reserpine, or amphetamine derivative, within 6 months of Screening. 5.Current treatment with anticoagulants (e.g., coumadin, heparin) that might preclude safe completion of the lumbar puncture. 6.Condition that precludes the safe performance of routine lumbar puncture, such as prohibitive lumbar spinal disease, bleeding diathesis, or clinically significant coagulopathy or thrombocytopenia. 7.Use of investigational drugs or devices within 60 days prior to Baseline (dietary supplements taken outside of a clinical trial are not exclusionary,e.g., coenzyme Q10). Healthy Control (HC) Subjects: 1.Current or active neurological disorder. 2.First degree relative with idiopathic PD (parent, sibling, child). 3.MoCA score = 26. 4.Received any of the following drugs that might interfere with DAT imaging: Neuroleptics, metoclopramide, alpha methyldopa, methylphenidate, reserpine, or amphetamine derivative, within 6 months of Screening. 5.Current treatment with anticoagulants (e.g., coumadin, heparin) that might preclude safe completion of the lumbar puncture. 6.Condition that precludes the safe performance of routine lumbar puncture, such as prohibitive lumbar spinal disease, bleeding diathesis, or clinically significant coagulopathy or thrombocytopenia. 7.Use of investigational drugs or devices within 60 days prior to baseline (dietary supplements taken outside of a clinical trial are not exclusionary, e.g., coenzyme Q10).

Study & Design

Study Type
Interventional clinical trial of medicinal product
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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