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New PET tracer aims to spot Parkinson's protein in living brains
NCT ID NCT07348250
First seen Jun 27, 2026 · Last updated Jul 28, 2026 · Updated 2 times
Summary
This early-phase study tests a new imaging drug called [18F]MK-0947 that works with PET scans to show where a protein called α-synuclein builds up in the brain—a hallmark of Parkinson's disease. Researchers will check safety and how well the tracer works in 22 adults (some with Parkinson's, some healthy). If successful, this could lead to better tools for diagnosing and tracking Parkinson's.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- [18F]MK-0947 (a radioactive imaging drug for PET scans)
- What this could lead to
- If successful, this could lead to a new way to see Parkinson's-related protein buildup in the brain, helping doctors diagnose the disease earlier and track its progression.
- What could go wrong
- This is a very early, small study (22 people) focused on safety and imaging, not treatment. The tracer may not work as hoped, and results may not apply to all Parkinson's patients.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
-
Early phase 1
The earliest testing in people: a first look at safety, in a very small group.
- Participants
-
16 people
The number who actually took part.
- Started
-
Dec 2025
- Finished
-
Jul 2026
- Lead sponsor
-
Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
-
18 to 80 years
- Sex
-
Anyone
- Healthy volunteers
-
Accepted
You do not need to have the condition being studied to take part.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Signed informed consent prior to any study procedures * Women of childbearing potential: abstinent or use 2 contraception methods (one barrier) during study and 90 days post last injection * Men: use 2 contraception methods and refrain from sperm donation during study and 90 days post last injection * PD \& HE participants: Age 40-80 years; HP participants: Age 18-50 years * Adequate circulation and normal clotting for arterial cannulation (if applicable) * HE participants: no neurological disorder, no first-degree relative with idiopathic PD * HP participants: healthy with no clinically relevant findings Exclusion Criteria: * Unwilling or unable to provide informed consent * Clinically significant hepatic, renal, cardiovascular, pulmonary, or systemic illness * Pregnant or breastfeeding * Contraindication to PET or MRI procedures (e.g., implants, claustrophobia) * History of severe allergic reactions to PET tracers or related compounds * Current or prior participation in investigational drug study within 30 days * Any condition that may interfere with study conduct or participant safety
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
-
Invicro (dba Perceptive)
New Haven, Connecticut, 06510, United States
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