About this trial

It is hypothesize that patients with clinically diagnosed neurodegenerative diseases will have significantly different receptor occupancy of 5HT2A receptors compared to a healthy age/sex-matched control group. This will be tested by measuring 5HT2A receptor density using the PET radioligand (R)-\[18F\]MH.MZ in both populations.

Eligibility criteria

Qualifiers

Patient arm - clinical diagnosis of Parkinson disease, diffuse Lewy body disease, multiple systems atrophy, Huntington's Disease, Frontotemporal Dementia, and other variants

Healthy arm - age and gender matched to patient arm

Psychosis (presence of hallucinations or delusions) starting after the diagnosis of Parkinson's disease, occurring at least weekly for 4 weeks, severe enough to warrant treatment.

Study partner available for study visits

Disqualifiers

Prior stroke or other uncontrolled serious neurological or medical illness

Contra-indication or inability to tolerate MRI scan

Use of serotonergic medications in the last 6 weeks

Incapable of providing independent consent.

Trial design

Treatments tested in this trial

  • Pimavanserin

Treatment groups

75 Participants
are divided into 1 treatment group

Locations

1
Vanderbilt University Medical Center37212, NashvilleTennessee, United States

Sponsors and collaborators

Vanderbilt University Medical Center

Lead sponsor

ACADIA Pharmaceuticals Inc.

Collaborator