Phase
Condition
N/ATreatment
Pimavanserin 10mg
Placebo
Clinical Study ID
Ages 18-45 All Genders Accepts Healthy Volunteers
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
Willing and able to give informed consent for participation in the research
Aged 18-45 years
Good vision and hearing
Body mass index (BMI) within the range of 18-35kg/m2 (This is to ensure anappropriate pharmacokinetic profile for pimavanserin is achieved by allparticipants)
Sufficiently fluent in English to understand tasks
Willing to avoid drinking any alcohol the day before the research visit
Exclusion
Exclusion Criteria:
Currently receiving or seeking treatment for any mental health condition
Any past or current history of severe and/or serious psychiatric disorder, includingbut not limited to schizophrenia, psychosis, bipolar affective disorder, severemajor depressive disorder, obsessive compulsive disorder (covered in SCID-5assessment in screening procedures)
ADHD requiring treatment with stimulant or other centrally-acting drugs
Regular alcohol consumption of more than 21 units per week
A head injury causing concussion or unconsciousness in the past 6 months
Pregnancy / intention to become pregnant during the study or breastfeeding
Any use of recreational drugs in the last three months
Participation in any other drug study in the last three months
Participation in any other study with the same tasks in the last year
History of cardiac disease or cardiac arrhythmias
Prolonged QTc interval on baseline ECG
Current usage of other drugs known to prolong QT interval including Class 1A or 3antiarrhythmics, e.g. certain antibiotics (getifloxacin, moxifloxacin)
Current use of drugs that inhibit CYP3A4 (eg Clarithromycin. Diltiazem.Erythromycin. Fluconazole). Participants will be asked to avoid grapefruit juice inthe week before the study.
Current use of psychoactive medication that in the opinion of the Chief Investigatormay interfere with the study measures
History of, or current medical condition(s) which, in the opinion of theInvestigator may interfere with the safety of the participant or the scientificintegrity of the study, including epilepsy/seizures, brain injury, severe hepatic orrenal disease, severe gastro-intestinal problems, Central Nervous System (CNS)tumours, severe neurological problems (e.g. Parkinson's disease; blackouts requiringhospitalisation);
Any physical (including visual and auditory), cognitive or language impairment thatwould make complying with the study protocol challenging
Excessive caffeine consumption, i.e., consumption higher than 8 cups of standardcaffeinated drinks (tea, instant coffee) or higher than 6 cups of stronger coffee orother drinks containing methylxanthines such as coca cola or Red Bull per day;
Smoking >10 cigarettes per day; or equivalent nicotine consumption
Participant who is unlikely to comply with the clinical study protocol or isunsuitable for any other reason, in the opinion of the chief investigator.
Inability to ingest up to 95mg of lactose
Additional Exclusion Criteria for Participants in the Sleep Study Cohort:
Unable to undergo cardiac monitoring
Unable to wear the sleep patch device for full monitoring period
Implanted neurostimulator
Study Design
Study Description
Connect with a study center
Department of Psychiatry, University of Oxford
Oxford,
United KingdomActive - Recruiting
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