Predict Parkinson progression with scan

Trial ID
NCT07380204
Official Title
In Vivo Quantification of Hsp90 in the Human Brain in Healthy Aging and Neurodegeneration Using the Novel PET Radioligand [11C]HSP990
Goal
Predict Parkinson progression with scan
Phase
NA
Status
RECRUITING
Sponsor
Universitaire Ziekenhuizen KU Leuven
Study Type
INTERVENTIONAL
Enrollment
48 participants
Conditions
Parkinson's Disease (PD), Alzheimer's Disease (AD), Amyotrophic Lateral Sclerosis (ALS)
Interventions
[11C]HSP990 PET dosimetry, [11C]HSP990 PET test-retest, [11C]HSP990 simplified scan protocol

Plain-Language Summary

The goal is to map and measure Hsp90, a cellular "chaperone" protein that helps fold and clear damaged proteins, in the brains of people with Parkinson's, Alzheimer's, ALS, and healthy aging to learn how Hsp90 changes with neurodegeneration. The approach uses PET imaging with a new radioligand called [11C]HSP990 that binds Hsp90 so researchers can see where and how much of the protein is present; parts of the study check radiation dose, how reproducible the scans are, and whether the scan can be shortened. This is an imaging test, not a treatment, so it does not alter medications like levodopa. Eligible participants include people with clinically established Parkinson's aged 45 to 85 in Hoehn‑Yahr stages 1,3 with a prior abnormal DaT scan, people meeting diagnostic criteria for AD or ALS, and healthy volunteers roughly 18 to 70 who pass medical and MRI screening and can lie still for the scan.

Locations

  • UZ Leuven, Leuven, Vlaam-Brabant, Belgium

Frequently Asked Questions

What is this trial testing?
This trial is studying [11C]HSP990 PET dosimetry. The goal is to map and measure Hsp90, a cellular "chaperone" protein that helps fold and clear damaged proteins, in the brains of people with Parkinson's, Alzheimer's, ALS, and healthy aging to learn how Hsp90 changes with neurodegeneration. The approach uses PET imaging with a new radioligand called [11C]HSP990 that binds Hsp90 so researchers can see where and how much of the protein is present; parts of the study check radiation dose, how reproducible the scans are, and whether the scan can be shortened. This is an imaging test, not a treatment, so it does not alter medications like levodopa. Eligible participants include people with clinically established Parkinson's aged 45 to 85 in Hoehn‑Yahr stages 1,3 with a prior abnormal DaT scan, people meeting diagnostic criteria for AD or ALS, and healthy volunteers roughly 18 to 70 who pass medical and MRI screening and can lie still for the scan.
Who can participate?
Participants must be between 18 Years and 70 Years.
Where is this trial located?
This trial is recruiting at 1 location.
Does it cost anything to join?
No. There is no cost to participate. Study-related care and treatment are provided at no charge.
How long does the trial last?
This trial is estimated to last approximately 3 years and 3 months.

View on ClinicalTrials.gov