Expanded Access of Pimavanserin for Patients With PD Psychosis
Primary Purpose
Parkinson's Disease Psychosis
Status
Approved for marketing
Phase
Locations
Study Type
Expanded Access
Intervention
Pimavanserin tartrate
Sponsored by
About this trial
This is an expanded access trial for Parkinson's Disease Psychosis
Eligibility Criteria
Inclusion Criteria:
Patient meets one of the following criteria:
- Patient has participated in a previous study of pimavanserin for Parkinson's disease psychosis (PDP)
- New ("De novo") patients
- A clinical diagnosis of Parkinson's disease with a minimum duration of 1 year
- Female patients must be of non-childbearing potential
- Psychotic symptoms must have developed after Parkinson's disease diagnosis was established
- Patient that has received stereotaxic surgery for subthalamic nucleus deep brain stimulation must be at least 6 months post-surgery and the stimulator settings must have been stable for at least 1 month prior to Study Day 1 (Baseline) and must remain stable during the trial
- The patient or Legally Authorized Representative (LAR) is willing and able to provide consent
- The patient or LAR is willing and able to adequately communicate in English.
Exclusion Criteria:
- Patient has a history of significant psychotic disorders prior to or concomitantly with the diagnosis of Parkinson's disease including, but not limited to, schizophrenia or bipolar disorder
- Patient has had dementia prior to or concurrently with their diagnosis of Parkinson's disease that may be inconsistent with a Parkinson's diagnosis
- Patient has current evidence of a serious and/or unstable cardiovascular, respiratory, gastrointestinal, renal, hematologic, or other medical disorder, including cancer or malignancies, which would affect the patient's ability to participate in the program
- Patient has had a myocardial infarction in last six months
- Patient has any surgery planned during the screening, treatment, or follow-up periods
Patients will be evaluated at screening to ensure that all criteria for study participation are met. These evaluations will include specific measures of psychosis severity, delirium, dementia, cardiovascular condition, and pregnancy status. Patients may be excluded from the study based on these assessments (and specifically if it is determined that their baseline health and psychiatric condition do not meet all pre-specified entry criteria).
Sites / Locations
Outcomes
Primary Outcome Measures
Secondary Outcome Measures
Full Information
NCT ID
NCT02762591
First Posted
May 3, 2016
Last Updated
April 17, 2017
Sponsor
ACADIA Pharmaceuticals Inc.
1. Study Identification
Unique Protocol Identification Number
NCT02762591
Brief Title
Expanded Access of Pimavanserin for Patients With PD Psychosis
Official Title
Expanded Access Program of Pimavanserin in Patients With Parkinson's Disease Psychosis
Study Type
Expanded Access
2. Study Status
Record Verification Date
April 2017
Overall Recruitment Status
Approved for marketing
Study Start Date
undefined (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
undefined (undefined)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
ACADIA Pharmaceuticals Inc.
4. Oversight
5. Study Description
Brief Summary
The purpose of this program is to provide patients with PDP access to pimavanserin until the product receives marketing approval from the FDA and is commercially available.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Parkinson's Disease Psychosis
7. Study Design
8. Arms, Groups, and Interventions
Intervention Type
Drug
Intervention Name(s)
Pimavanserin tartrate
Intervention Description
Pimavanserin tartrate 40 mg, tablet, taken as two 20 mg tablets, once daily by mouth
10. Eligibility
Sex
All
Minimum Age & Unit of Time
40 Years
Eligibility Criteria
Inclusion Criteria:
Patient meets one of the following criteria:
Patient has participated in a previous study of pimavanserin for Parkinson's disease psychosis (PDP)
New ("De novo") patients
A clinical diagnosis of Parkinson's disease with a minimum duration of 1 year
Female patients must be of non-childbearing potential
Psychotic symptoms must have developed after Parkinson's disease diagnosis was established
Patient that has received stereotaxic surgery for subthalamic nucleus deep brain stimulation must be at least 6 months post-surgery and the stimulator settings must have been stable for at least 1 month prior to Study Day 1 (Baseline) and must remain stable during the trial
The patient or Legally Authorized Representative (LAR) is willing and able to provide consent
The patient or LAR is willing and able to adequately communicate in English.
Exclusion Criteria:
Patient has a history of significant psychotic disorders prior to or concomitantly with the diagnosis of Parkinson's disease including, but not limited to, schizophrenia or bipolar disorder
Patient has had dementia prior to or concurrently with their diagnosis of Parkinson's disease that may be inconsistent with a Parkinson's diagnosis
Patient has current evidence of a serious and/or unstable cardiovascular, respiratory, gastrointestinal, renal, hematologic, or other medical disorder, including cancer or malignancies, which would affect the patient's ability to participate in the program
Patient has had a myocardial infarction in last six months
Patient has any surgery planned during the screening, treatment, or follow-up periods
Patients will be evaluated at screening to ensure that all criteria for study participation are met. These evaluations will include specific measures of psychosis severity, delirium, dementia, cardiovascular condition, and pregnancy status. Patients may be excluded from the study based on these assessments (and specifically if it is determined that their baseline health and psychiatric condition do not meet all pre-specified entry criteria).
12. IPD Sharing Statement
Learn more about this trial
Expanded Access of Pimavanserin for Patients With PD Psychosis
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