Open-label Study to Evaluate Brain α-Synuclein Deposition Using PET and [18F]MK-0947 in Parkinson's Disease

Stopped early · Early Phase 1

Conditions studied: Parkinson's Disease (PD), Parkinson's Disease, Parkinson's Disease (Disorder)

In brief

This clinical study is being conducted to learn more about a new imaging drug called \[18F\]MK-0947, which is designed to help doctors see changes in the brain related to Parkinson's disease (PD). PD is a condition that affects movement, balance, and thinking. The drug works with a type of scan called PET (Positron Emission Tomography) to show areas of the brain where a protein called α-synuclein builds up. This buildup is linked to PD and other brain disorders. The main goal of this study is to find out if \[18F\]MK-0947 is safe for people and if it works well to show α-synuclein in the brain. The study will also look at how the drug moves through the body and how much radiation it gives off. Researchers hope this information will help develop better tools for diagnosing PD and tracking how it changes over time. Who can join? Adults who have PD or who are healthy may be able to take part. Participants will have screening tests to make sure they qualify. What does participation involve? People in the study will have PET scans, blood tests, and other safety checks. Some participants will also have an MRI scan. The study is divided into two parts: Part 1 looks at how the drug works in the brain of PD patients and healthy elderly participants, and Part 2 measures radiation levels in healthy participants. Why is this important? There is currently no cure for PD, and better imaging tools could help researchers develop new treatments. By joining this study, participants will help advance research that may improve care for people with PD and similar conditions in the future.

Key facts

Study ID: NCT07348250
Run by: Invicro
People needed: 16
Starts: 2025-12-08
Expected to finish: 2026-07-20
Last updated by the study team: 2026-07-27

Who can join

Age: 18 and older, up to 80. Sex: any. Healthy volunteers: accepted.

You may qualify if…

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

You may not qualify if…

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

Where it is running

Invicro (dba Perceptive) — New Haven, Connecticut, United States

Full record on ClinicalTrials.gov

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