[18F]MC225-PET in Neurodegenerative Disease
Primary Purpose
Neurodegenerative Diseases, Alzheimer Disease, Parkinson Disease
Status
Recruiting
Phase
Phase 1
Locations
Netherlands
Study Type
Interventional
Intervention
[18F]MC225
Sponsored by
About this trial
This is an interventional diagnostic trial for Neurodegenerative Diseases focused on measuring PET, pharmacokinetic modeling, [18F]MC225
Eligibility Criteria
Inclusion Criteria: Patient is diagnosed with Alzheimer's disease, Parkinson's disease or Mild Cognitive Impairment Exclusion Criteria: Use of any medication influencing the P-glycoprotein function History of neuropsychiatric disorders Contra-indications MRI Allergy contrast agent
Sites / Locations
- University Medical Center GroningenRecruiting
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm Type
Active Comparator
Active Comparator
Active Comparator
Arm Label
Alzheimer's disease
Mild Cognitive Impairment
Parkinson's disease
Arm Description
Patients diagnosed with Alzheimer's disease
Patients diagnosed with Mild Cognitive Impairment
Patients diagnosed with Parkinson's disease
Outcomes
Primary Outcome Measures
P-glycoprotein function
The function of P-glycoprotein at the blood-brain barrier measured by PET tracer-uptake (volume of distribution) in the brain
Secondary Outcome Measures
Full Information
NCT ID
NCT05853471
First Posted
November 9, 2022
Last Updated
May 9, 2023
Sponsor
University Medical Center Groningen
1. Study Identification
Unique Protocol Identification Number
NCT05853471
Brief Title
[18F]MC225-PET in Neurodegenerative Disease
Official Title
Evaluation of [18F]MC225-PET to Measure P-glycoprotein Function in Neurodegenerative Disease
Study Type
Interventional
2. Study Status
Record Verification Date
May 2023
Overall Recruitment Status
Recruiting
Study Start Date
February 1, 2022 (Actual)
Primary Completion Date
January 1, 2024 (Anticipated)
Study Completion Date
January 1, 2024 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University Medical Center Groningen
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
P-glycoprotein, an efflux transporter at the blood-brain barrier plays an important role in de development of neurodegenerative disease. A novel PET tracer ([18F]MC225) was developed to measure the function of P-glycoprotein and was tested with succes in healthy volunteers. This study aims to evaluate [18F]MC225 in neurodegenerative disease.
Detailed Description
A decrease in P-glycoprotein (P-gp) function is associated with the onset of neurodegenerative disease. New treatment strategies in neurodegenerative disease, including Parkinson's disease and Alzheimer's disease, aim to restore the P-gp function. To evaluate the effect of these potential therapies, measurement of the P-gp function is necessary. Up until now [11C]verapamil is considered to be the gold standard to measure P-gp function. However tracer uptake in the brain of [11C]verapamil is too low for adequate measurement of treatment effect, especially of restoring P-gp function. A novel PET tracer to measure P-gp function, [18F]MC225, has the potential advantage of higher brain uptake values at baseline and might therefore able to measure both up- and down regulation P-gp function. [18F]MC225 was recently studied in healthy volunteers and a method to quantify P-gp function was developed. This study aims to evaluate [18F]MC225 to measure P-gp function in neurodegenerative disease.
To this aim 10 MCI patients, 10 patients with Alzheimer's disease and 10 Parkinson's disease patients will be included and undergo one 60 min dynamic [18F]MC225 PET scan, combined with a 10 min [15O]H2O PET. Tracer uptake values (Vt) and influx (K1) in several brain regions of interest, representing local P-gp function will be compared with the [18F]MC225 uptake values in the brain of healthy volunteers obtained in a previous study.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Neurodegenerative Diseases, Alzheimer Disease, Parkinson Disease, Mild Cognitive Impairment
Keywords
PET, pharmacokinetic modeling, [18F]MC225
7. Study Design
Primary Purpose
Diagnostic
Study Phase
Phase 1, Phase 2
Interventional Study Model
Parallel Assignment
Model Description
[18F]MC225 is administrated to patients in three groups to evaluate the P-glycoprotein function in these groups and compare the results with the P-gp function of healthy volunteers obtained in a previous study
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
30 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Alzheimer's disease
Arm Type
Active Comparator
Arm Description
Patients diagnosed with Alzheimer's disease
Arm Title
Mild Cognitive Impairment
Arm Type
Active Comparator
Arm Description
Patients diagnosed with Mild Cognitive Impairment
Arm Title
Parkinson's disease
Arm Type
Active Comparator
Arm Description
Patients diagnosed with Parkinson's disease
Intervention Type
Drug
Intervention Name(s)
[18F]MC225
Intervention Description
All participants will undergo a PET scan with [18F]MC225. No pharmaceutical effects are expected and the study will exclusively have a diagnostic purpose. However, since [18F]MC225 is a new PET tracer, it is included in pharmaceutical studies and any study performed with [18F]MC225 will be automatically be registered as intervention study.
Primary Outcome Measure Information:
Title
P-glycoprotein function
Description
The function of P-glycoprotein at the blood-brain barrier measured by PET tracer-uptake (volume of distribution) in the brain
Time Frame
60 minutes
10. Eligibility
Sex
All
Minimum Age & Unit of Time
50 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Patient is diagnosed with Alzheimer's disease, Parkinson's disease or Mild Cognitive Impairment
Exclusion Criteria:
Use of any medication influencing the P-glycoprotein function
History of neuropsychiatric disorders
Contra-indications MRI
Allergy contrast agent
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Pascalle Mossel, Msc
Phone
+31503616161
Email
p.mossel@umcg.nl
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Gert Luurtsema, Phd
Organizational Affiliation
University Medical Center Groningen
Official's Role
Principal Investigator
Facility Information:
Facility Name
University Medical Center Groningen
City
Groningen
ZIP/Postal Code
9713GZ
Country
Netherlands
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Pascalle Mossel, Msc
Phone
0503616161
Email
p.mossel@umcg.nl
12. IPD Sharing Statement
Plan to Share IPD
No
IPD Sharing Plan Description
No IPD will be shared with other researchers
Learn more about this trial
[18F]MC225-PET in Neurodegenerative Disease
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