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[18F]MNI-444 for Healthy Subjects
Phase 1
Waitlist Available
Led By David Russell, M.D., Ph.D
Research Sponsored by Invicro
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 1 year
Awards & highlights
Study Summary
This trial is testing if caffeine can help prevent Parkinson's by binding to receptors in the brain.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 1 year
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~1 year
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
To evaluate the pharmacodynamics of multiple doses of oral caffeine on striatal binding of the adenosine A2A receptor ligand [18F]MNI-444.
To evaluate the pharmacokinetics of multiple doses of oral caffeine on striatal binding of the adenosine A2A receptor ligand [18F]MNI-444.
Trial Design
1Treatment groups
Experimental Treatment
Group I: [18F]MNI-444Experimental Treatment1 Intervention
After a wash-out of caffeine of at least 24 hours, each participant will receive a single injection of [18F]MNI-444 followed by brain PET imaging of up to 90 minutes to establish baseline A2A receptor binding.
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
[18F]MNI-444
2021
Completed Phase 1
~10
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Logistics
Participation is compensated
You will be compensated for participating in this trial.
Who is running the clinical trial?
InvicroLead Sponsor
16 Previous Clinical Trials
382 Total Patients Enrolled
David Russell, M.D., Ph.DPrincipal InvestigatorInvicro
1 Previous Clinical Trials
130 Total Patients Enrolled
Frequently Asked Questions
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